Skip to main content

Signal transduction inhibitors in treatment of myelodysplastic syndromes


Myelodysplastic syndromes (MDS) are a group of hematologic disorders characterized by ineffective hematopoiesis that results in reduced blood counts. Although MDS can transform into leukemia, most of the morbidity experienced by these patients is due to chronically low blood counts. Conventional cytotoxic agents used to treat MDS have yielded some encouraging results but are characterized by many adverse effects in the predominantly elderly patient population. Targeted interventions aimed at reversing the bone marrow failure and increasing the peripheral blood counts would be advantageous in this cohort of patients. Studies have demonstrated over-activated signaling of myelo-suppressive cytokines such as TGF-β, TNF-α and Interferons in MDS hematopoietic stem cells. Targeting these signaling cascades could be potentially therapeutic in MDS. The p38 MAP kinase pathway, which is constitutively activated in MDS, is an example of cytokine stimulated kinase that promotes aberrant apoptosis of stem and progenitor cells in MDS. ARRY-614 and SCIO-469 are p38 MAPK inhibitors that have been used in clinical trials and have shown activity in a subset of MDS patients. TGF-β signaling has been therapeutically targeted by small molecule inhibitor of the TGF-β receptor kinase, LY-2157299, with encouraging preclinical results. Apart from TGF-β receptor kinase inhibition, members of TGF-β super family and BMP ligands have also been targeted by ligand trap compounds like Sotatercept (ACE-011) and ACE-536. The multikinase inhibitor, ON-01910.Na (Rigosertib) has demonstrated early signs of efficacy in reducing the percentage of leukemic blasts and is in advanced stages of clinical testing. Temsirolimus, Deforolimus and other mTOR inhibitors are being tested in clinical trials and have shown preclinical efficacy in CMML. EGF receptor inhibitors, Erlotinib and Gefitinib have shown efficacy in small trials that may be related to off target effects. Cell cycle regulator inhibitors such as Farnesyl transferase inhibitors (Tipifarnib, Lonafarnib) and MEK inhibitor (GSK1120212) have shown acceptable toxicity profiles in small studies and efforts are underway to select mutational subgroups of MDS and AML that may benefit from these inhibitors. Altogether, these studies show that targeting various signal transduction pathways that regulate hematopoiesis offers promising therapeutic potential in this disease. Future studies in combination with high resolution correlative studies will clarify the subgroup specific efficacies of these agents.



Myelodysplastic syndromes (MDS) encompass a spectrum of hematologic diseases characterized by ineffective hematopoiesis in the marrow that leads to refractory cytopenia. Based on the degree of cytopenia and malignant potential, MDS can be classified as low or high grade subtypes, using the International Prognostic Scoring System [1]. In low grade MDS, marrow hyper cellularity and peripheral cytopenia are commonly seen due to upregulated apoptosis in the progenitor stem cells. However decreased apoptosis is seen during transformation to higher risk MDS, which often manifests with an increase in myeloblasts [2]. Most patients present with low risk disease and experience morbidity due to anemia, neutropenia or thrombocytopenia. Strategies to raise blood counts are needed to alleviate morbidity in these patients. Despite numerous advances, better understanding of pathways regulating hematopoiesis is still lacking. Since cytokines are important in regulating differentiation of hematopoietic cells, targeting them appears to be a rational therapeutic strategy in MDS. Various studies suggest Tumor Necrosis factor α(TNF α) [3], Transforming Growth Factor β(TGF β) [4], Vascular endothelial Growth Factor (VEGF) [5], Activin receptor like kinase (ALK) [6], Interleukins(ILs) [7], and Interferons(IFN) [8] regulate the bone marrow milieu in MDS. The physiologic effects of a few of these cytokines are executed by the support of transcription regulators like the JAK-STAT pathway and many other pathways [9]. Hence strategies that can balance the effects of the stimulatory and inhibitory cytokine pathways can potentially be of therapeutic utility in MDS and other hematologic neoplasm [10, 11].

Cytokine regulation of hematopoiesis

A complex interplay of various cytokines has been implied in maintaining normal hematopoiesis. Growth factors such as erythropoietin (EPO), Granulocyte macrophage colony stimulating factor (GM-CSF), Granulocyte colony stimulating factor (G-CSF) and Interleukin-3 promotes the differentiation of erythroid and myeloid progenitors [12]. On the other hand, Interferons, Interleukins, TGF-β and TNF-α have inhibitory actions on hematopoietic stem cells (Figures 1 and 2). It is conceivable that an imbalance between the action of inhibitory and stimulatory cytokines can lead to increased myelo-suppression and bone marrow failure. In fact, excessive signaling of inhibitory cytokines is seen in MDS, thus making these pathways a potential target for therapy.

Figure 1
figure 1

Regulation of hematopoiesis by cytokines. The process of differentiation of hematopoietic stem cells into mature blood cells is tightly regulated by the actions of both stimulatory and inhibitory cytokines.

Figure 2
figure 2

Model for pathogenesis of MDS. A mutation or epigenetic alteration in hematopoietic stem cells (HSC), leads to generation of pro-inflammatory milieu in marrow microenvironment that can result in apoptotic cell death of normal HSCs. Inhibition of myelo-suppressive cytokine signaling cascades can stimulate hematopoietic activity in HSCs.

P38 Mitogen Activated Protein (MAP) Kinase - Therapeutic target in MDS

Various inhibitory cytokines can activate the p38 MAPK pathway in the hematopoietic progenitor cells (Figure 3). In prior studies we have shown that this pathway is constitutively activated in MDS [1315]. Activation of p38 MAPK was seen in a large proportion of bone marrow cells of patients with low grade MDS, with a greater number of phospho-p38-positive staining cells and significantly higher intensity of immunohistochemical staining when compared to anemic non-MDS controls. We also determined that p38 MAPK activation mediates enhanced progenitor cell apoptosis seen in MDS bone marrows. Thus blocking this pathway is a potential therapeutic strategy that can lead to decrease in apoptosis and enhanced survival of hematopoietic stem and progenitor cells.

Figure 3
figure 3

Mitogen activated protein kinases. These are evolutionarily conserved protein kinases that regulate many important physiological processes. The p38 MAP kinase regulates cell death and proliferation in hematopoietic cells.

The compound SCIO-469, was the first small molecule inhibitor of the p38 MAPK that was tested clinically in MDS [16]. By predominantly inhibiting the alpha isoform (dominant isoform in MDS) of the P38 MAPK, this compound could stimulate hematopoiesis from MDS progenitors in vitro [17]. A phase 1/ 2 multi center trial of SCIO- 469 (N-62) was conducted in patients with low to intermediate risk MDS [18]. Patients in this trial received SCIO-469 at doses of 30 mg TID (n-15), 60 mg TID (n-15) and 90 mg TID (n-15). Due to the fact that the maximum tolerable dose was not achieved, an additional arm with 120 mg TID dosing (n-17) was added to the trial. Based on International Working Group criteria, responders were evaluated with an intention to continue using the drug until a maximum of 104 weeks of therapy. Of the 62 patients enrolled in the study only 47 of them completed the treatment till week 16. Only 12 of these patients were able to continue therapy after week 16 and 5 of them completed treatment till week 52. About 29% of patients (18 out of 62) experienced HI in each of the hematopoietic lineage. Amongst 62 study recruited patients, erythroid (6 major, 5 minor), neutrophil (3 major, 3 minor) and platelets (1 major) response were documented. Five patients were found to have progression of disease, 36 patients had stable disease and 1 patient achieved a cytogenetic response. Hence it was concluded that SCIO- 469 was found to be modestly active as a monotherapy in low- int risk MDS and recommended further studies at higher doses.

More recently, another p38 MAPK inhibitor, ARRY-614, has shown promising activity in MDS. This compound can block both the p38 MAPK and the Tie-2 pathway. Tie-2 pathway has been noted to complement P38 MAP kinase pathway in cytokine regulation and phenotypic maturation of hematopoietic stem cells [19]. Tie-2 ligands have been found to be over-expressed in marrows of MDS patients and higher expression of Tie-2 has been correlated as a poor prognostic indicator [20]. A phase I trial of Arry-614 in low (n-11)/int-1(n-34) risk, heavily pretreated cohort of MDS patients was conducted recently [21]. In the inclusion criterion, prior therapies with erythropoietin stimulating agents (49%), hypo-methylating agents (82%) and lenalidomide (40%) were permitted. ARRY- 614 at doses of 400-1200 mg once daily and 200-300 mg twice daily was administered in fasting state patients and a dose of 400 mg daily was tested in non- fasting state. Of the 43 evaluable patients, hematological improvement was noted in 8 patients (erythroid- 4, platelet-4 and neutrophil-5). Interestingly 5 bilineage improvement in counts was reported. Also the study demonstrated that ARRY-614 decreased the baseline elevated EPO levels and reduced platelet transfusions in patients who had failed therapy with hypomethylating agents. Hence it was hypothesized by the authors that addition of recombinant EPO in combination with ARRY- 614 may further optimize erythroid responses. Correlative studies showed that treatment with ARRY-614 resulted in an 85% reduction of phosphorylated/activated-p38 levels in the marrow along with concomitant decreased apoptosis [22]. Based on encouraging responses, particularly in patients that failed hypo-methylating agents, further clinical studies are being planned with this drug.

Transforming Growth Factor- β (TGF- β) inhibitors

The role of TGF- β cytokine on inhibition of normal stem and progenitor cells is well documented [23]. TGF-β binds to a set of TGF-β receptors and lead to activation of intracellular SMAD 2/3 proteins. These proteins associate with other cofactors and translocate to the nucleus to mediate the biological actions on stem cells. We have demonstrated that smad2, a downstream mediator of TGF-β receptor I kinase (TBRI) activation, is constitutively activated and over expressed in MDS bone marrow precursors [24]. Furthermore, we showed that shRNA mediated down regulation as well as pharmacologic inhibition of TBRI leads to enhanced hematopoiesis in a variety of MDS subtypes in vitro. TBRI kinase inhibition also alleviated anemia and stimulated hematopoiesis in a mouse model of bone marrow failure, demonstrating it as a potential therapeutic target in MDS [4]. These studies provided a preclinical rationale for targeting TGF-β signaling pathways in MDS.

LY2157299 is a novel small molecule that specifically inhibits the kinase activity of the Transforming Growth Factor- β Type I Receptor (TGF- β RI) and its downstream signaling pathway. In vitro and In vivo studies have shown the efficacy of LY2157299 in stimulating hematopoiesis in MDS [25], thus providing the rationale for using this drug in MDS (Figure 4). This agent is clinically relevant and has shown adequate safety signals in phase I studies in solid tumors [26]. This agent is also being tested clinically in gliomas and will be evaluated in MDS in the near future.

Figure 4
figure 4

TGF-β signaling pathway. TGF-β receptors after binding with the TGF-β ligand, forms a receptor- ligand complex. This dimerization activates the kinase domain of Type I receptor. The activated Type 1 receptor kinase further activates the downstream smad complexes to regulate gene transcription. LY2157299 inhibits the TGF-β receptor I kinase and can reverse the cellular effects of TGF- β signaling pathway in hematopoietic cells.

Activin and TGF-beta receptor ligand traps

The stimulatory role of erythropoietin (EPO) in erythropoiesis has been well established [27]. Hematopoietic cells in MDS are usually resistant to EPO and increased EPO level, reflecting a refractory state to therapy is often seen in the long course of this disease [28]. Consequently, only a minority of patients respond to recombinant EPO [29]. Activin family members belong to the TGF-superfamily ligands and plays important roles in cellular development of many different tissues including the hematopoietic tissue [30]. Hence compounds that can regulate Activin mediated hematopoietic activity have been tested for clinical applicability in MDS. ACE-536 is a modified type-II Activin receptor fusion protein and serves as a ligand trap for TGF- β family members that are involved in erythroid differentiation. Preclinical trials in C57BL/6 mice were associated with rise in hematocrit, red blood cells and hemoglobin parameters at doses of 10 mg/kg. The authors of this study observed a rapid proliferation of late stages of erythroid precursors, independent of EPO mediated mechanisms [31]. The encouraging stimulation of erythropoiesis observed led to further tests in the NUP98/HOX murine model of MDS [32]. When RAP-536 (The murine homolog of human ACE-536) was injected at 10 mg/kg, twice a week for 8 months, it led to significant improvements in hematologic parameters in comparison to control studied. Authors reported that progression of anemia was much slower in mice treated with RAP-536 (8.3% vs. 22% in HCT and 13% vs. 30% in RBC). Lack of increased blasts detected probably suggests a reduction in transformation to leukemia with RAP-536 treatment [33]. Currently a few phase-1/2 studies (Table one) are evaluating the role of ACE-536 in treating anemia.

Sotatercept (formerly known as ACE- 011) (fusion protein of Human soluble Activin receptor type-IIA and Fc- portion of human IgG1) [34] is another ligand trap that has been shown to inhibit the inhibitory SMAD2/3 signaling in hematopoietic cells [35]. A recent clinical report of sotatercept in cancer patients and healthy volunteers has shown a rapid rise in hemoglobin and reticulocyte counts [36]. Various clinical trials (NCT01464164, NCT01571635 and NCT01736683) have been initiated and will explore the efficacy of this agent in treating anemia associated with marrow failure syndromes.

Multi kinase inhibitor

Onconova-01910.Na (Rigosertib) is a multi-kinase inhibitor of Polo like kinase, Akt and PI3 kinase pathways [37]. It appears to have selectivity for tumor cells containing these activated pathways and can cause apoptosis by inducing mitotic arrest at G2/M phase of cell cycle [38]. Preclinical studies in MDS demonstrated that ON-01910 could induce selective apoptosis in myeloid cells with trisomy of chromosome 8. Trisomy 8 is a frequent cytogenetic alteration in MDS and is associated with upregulation of cyclin D1 and c-myc proteins, which drive cellular proliferation. Treatment of primary MDS samples containing trisomy 8 with ON-01910 showed a reduction in CD34+ blasts in the first Phase 1 (NCT00533416) study conducted [39]. The trial included 12 patients with High risk MDS and 2 AML patients with trisomy-8. As reported in the study, 3 patients had greater than 50% reduction in blast counts & 3 patients achieved hematologic improvement as per IWG criteria. All patients that showed a hematologic response to ON-01910 had reduced expression of cyclin D1 in CD34+ cells post therapy [39]. A more recent trial with Rigosertib in 60 MDS patients demonstrated the ability of this drug in reducing blasts and also revealed a positive correlation between bone marrow response and overall survival [40]. The encouraging results offered by this study have prompted an ongoing phase 3 study in MDS patients who have failed hypo-methylating agent therapy.

Mammalian target of rapamycin inhibitors (mTOR inhibitors)

The PI3K/mTOR pathway is an intracellular signaling pathway that is well studied in various cancers [41]. PI3K is a serine/threonine protein kinase that acts as a fulcrum and interface for various downstream pathways concerned with cell proliferation and metabolism [42, 43]. By controlling enzymatic activity and decreasing angiogenesis, mTOR inhibitors have shown antiproliferative effects in various malignancies [44]. Preclinical studies have shown the oncogene, Ecotropic Viral Integration Site 1(EVI1) [45], a nuclear transcription factor is necessary for hematopoietic stem cell proliferation & differentiation. In MDS and myeloid malignancies with EVI1 translocations, this transcription factor can cause PTEN repression and activation of PI3K/mTOR pathways [46], thereby leading to increased cell proliferation and reduced differentiation. Hence, many mTOR inhibitors are being studied as a novel strategy in treating MDS and other hematologic malignancies. Deforolimus has been studied in relapsed or refractory hematologic malignancies and has shown antitumor activity [47]. Temsirolimus is currently being evaluated in the TEMDS (Temsirolimus in MDS Study) trial (NCT 01111448). Unfortunately, NCT 00809185 which was meant to evaluate everolimus in MDS was terminated due to slow accrual. Despite this initial set back, with results of many studies yet to be presented, the role of mTOR inhibition could still hold promise in MDS [48].

Epithelial Growth Factor Receptor (EGFR) inhibitors

The arrival of EGFR inhibitors in clinical practice has significantly changed the landscape of lung cancer treatment in modern era and a similar attempt to replicate this success is tried in other cancers [49, 50]. An interesting report of Gefitinib induced differentiation in AML cell lines and AML patient samples [51], spurred preclinical studies that reported pro apoptotic and anti-mitotic effects of erlotinib in EGFR negative MDS and AML cell lines [52]. This off target effect of EGFR inhibitor was attributed to blockage of Jak2/Stat-5 pathway in subsequent experiments [53]. A phase 2 study of erlotinib in MDS was reported at ASH 2010 [54]. In this study, patients who received Tarceva had failed prior Azacytadine or Decitabine. Amongst 23 reportable study patients who received 150 mg Erlotinib tablets daily for 16 weeks, 3 went into CR, 1 showed hematologic improvement and 6 had stable disease. 4 patients died in the study arm. Diarrhea, platelet disorders and rash were commonly observed adverse events. Currently there is an ongoing NCT 1085838 clinical trial that is looking further into the role of erlotinib in High risk MDS. These studies have now been followed up by preclinical evaluation of combining erlotinib with azacytadine [55]. Another preclinical study reported that the combination of erlotinib with chemotherapeutic agents, leads to increased chemosensitivity in AML cell lines. This synergistic effect observed was achieved by promoting apoptosis and inhibiting the drug efflux from cells via inhibition of the ABC transporters [56]. Based on these pre clinical studies further clinical studies are being designed to explore combinations of EGFR inhibitors with other agents.

Ezatiostat (TLK199) (Glutathione S Transferase1-1 inhibitor)

The enzyme GSTP1-1 (GSTP- Glutathione S Transferase pi1) can bind and inhibit the Jun Kinases with subsequent impact on growth and differentiation of healthy hematopoietic stem cells and cancer cells [57]. Ezatiostat is structurally analogous to Glutathione and can displace it from the glutathione binding site needed to inhibit the Jun Kinase pathways. Hence Ezatiostat acts as a Glutathione S-Transferase P1-1 inhibitor and activates the pro apoptotic Jun kinase in cancer cells that express GSTP1-1[58]. This action promotes growth and maturation of normal hematopoietic progenitors and induces apoptosis in cancer cell lines. A recent phase 2 trial of Ezatiostat using 2 dosing schedules for heavily pretreated Low/Int-1 risk MDS (n-89) led to RBC transfusion reduction in 29% and independence in 11% of transfusion dependent population [59]. Liposomal preparation of the compound showed encouraging results in one other Phase 2 MDS study [60]. The oral formulation of the compound is currently being studied in del5q MDS (NCT01422486). Since there are limited effective therapeutic options in non- del 5q MDS patients (low and intermediate-1 risk), Ezatiostat has been explored in combination with Lenalidomide in a phase-1 study. As per the design of this study patients received a starting dose of Lenalidomide 10 mg for every 21 days followed by a week break in combination with 2 grams/day Ezatiostat. Dose escalation of Ezatiostat to 2.5 grams/day without changing the dose of Lenalidomide was carried out to determine the maximal tolerable dose and to determine the efficacy of combination therapy measured in terms of hematologic improvement. Amongst the 2.5 grams/day Ezatiostat with 10 mg Lenalidomide receiving arm, about 25% of the patients experienced HI- E response. The HI- E response rate was 40% in 2 grams/day Ezatiostat arm and approximately 43% of patients who were red blood cell transfusion dependent prior to therapy become independent of transfusion post therapy. Also 60% of patients showed HI- P response. A significant proportion of bilineage (Erythroid/Platelet- 60%) (Erythroid/Neutrophil and Neutrophil/Platelet- 33%) response was observed in 2000 mg Ezatiostat arm. Interestingly, 33% of patients had trilineage improvement with this combination. The combination was well tolerated and found a limited amount of gastrointestinal disturbance and low blood counts as commonly observed adverse events [61]. This study provides further impetus to test Ezatiostat in future phase2 or 3 MDS studies, either as monotherapy or in combination with lenalidomide.

Farnesyl Transferase Inhibitors (FTI)

Farnesyl transferases regulate post translational farnesylation of protein substrates that are involved in cell signaling, proliferation and differentiation [62]. The oncogenic Ras protein requires post translational changes to become active in cancer cell lines with the help of the enzyme Farnesyl Transferase. Gain of function mutations in RAS are commonly seen with various cancers and this gene has been reported to be mutated in about approximately 20% of MDS patients [63]. Hence inhibitors of Farnesylation, that have shown antiangiogenic, antiproliferative and pro apoptotic functions in tumor cell lines [6466] are being studied in MDS.

Tipifarnib (R115777) was studied in a phase 1 setting by Kurzrock et al. who tried doses of 300 mg BID for 8 weeks schedule (3 weeks on and 1 week off). Of the 21 patients treated, only 4 of them had RAS mutation. Authors reported 30% objective response with 3 patients showing HI, 2 showing PR and 1 reaching complete remission. Interestingly, amongst the responders only 2 of these 6 patients had a RAS mutation. The maximal tolerable dose as per this study was 400 mg BID and myelo-suppression was a frequently reported side effect [67]. This was followed by a multicenter phase 2 study reported in 2004, where 28 patients received Tipifarnib. At doses of 600 mg BID the compound was tested for 4 weeks followed by 2 weeks break. Treatment was discontinued at the end of 2 cycles if therapeutic effect was observed. A dose reduction to 300 mg BID was allowed for toxicities. Once response was noted, patients were allowed to complete the induction regime for a total of 12 months. Three responders were observed in the trial (Complete-2, Partial-1). All responders had received an initial induction with R115777 of 600 mg BID followed by dose reduction to 300 mg BID after 12 weeks. Low neutrophil count, weakness, gastrointestinal upset were often reported adverse events in the study [68]. A subsequent phase 2 study reported in 2007 tested R115777 in int- high risk MDS. In this study a total of 82 patients received the compound at doses of 300 mg BID for 3 weeks followed by 1 week break from the compound. Of the 26 responders 12 had achieved CR, 14 had HI and about 45% (n-37) were noted to be in stable disease. The median response duration amongst patients who had achieved CR was about 11.5 months. Approximately 18% (neutropenia), (32%) thrombocytopenia and (18%) anemia was reported as drug related hematologic adverse events in this study [69].

Lonafarnib is another farnesyl transferase inhibitor that has been studied in MDS. In a phase 2 study, lonafarnib was studied in MDS and CMML patients (N-67) [70]. The drug was studied at doses of 200 mg BID and 300 mg BID. For patients who had greater than Grade 2 toxicity the dose was decreased to 150 mg BID after interruptions. In this trial, HI was noted in 6 MDS patients and 10 CMML patients. Diarrhea, fatigue and nausea were the commonly reported adverse events with this compound. However earlier treatment withdrawal was noted amongst patients in the trial and the authors recommended intermittent dosing frequencies to be tested in future trials. Another phase 2 trial reported a very small benefit of lonafarnib in MDS at doses of 200 mg BID for 3 courses of 4 weeks separated by 1–4 weeks of drug holiday [71]. With significant toxicity profile and modest benefit, lonafarnib needs to be further tested in large population studies and varied dosing schedule to find their clinical niche in MDS and AML.

Mek inhibitor

The binding of stimulatory growth factors can lead to the activation of Ras, Raf, MEK and ERK signaling cascades. These signaling cascades regulate proliferation, cell survival, angiogenesis and invasion [72]. Alteration in Mek/Raf/Erk has been found to promote abnormal cell growth in Kras mediated MDS/myeloproliferative neoplasm (CMML/JMML) [73]. Constitutively activated MAP/Erk kinase pathways in various cancers with activating mutations in the RAS oncogene are often associated with poor prognosis [74, 75]. Blocking Mek pathways in preclinical models of AML have resulted in growth inhibitory effects [76] and could potentially sensitize leukemic cells to chemotherapy induced apoptosis [77]. Mek kinase inhibitor, PD 0325901, has shown to improve erythropoiesis and rectify abnormal proliferation and differentiation pattern in mouse models of CMML and JMML [78]. A more recent study reported in ASCO 2011 demonstrated utility of MEK inhibition in relapsed/refractory myeloid neoplasm. GSK1120212 (Mek- inhibitor) was given at 2 mg daily dose to 45 patients with K or N RAS mutant MDS and led to an ORR of 31% and a CR rate of 23%. Approximately 54% of these patients exhibited stable disease [79]. The utility of MEK inhibitors in suppressing mutant RAS mediated abnormal myeloproliferation and its ability to suppress apoptosis is currently being tested in clinical trials (Table 1).

Table 1 Relevant signal transduction inhibitors clinical trials in MDS

TNF- α antagonist


The efficacy of anti-TNF-α strategies in inflammatory conditions like rheumatoid arthritis [80] encouraged the testing of these agents in MDS. Increased levels of TNF-α have been reported in MDS marrows and this cytokine has been implicated in increased apoptosis noted with the disease [81]. TNF α inhibition was first tested in a phase 2 study by Deeg et al, in 12 MDS patients. Patients enrolled in the study received Etanercept 25 mg s/c twice weekly dose with a plan to increase it to three times a week if there was no improvement in the counts by 8th week. The study showed Hematologic Improvement in 3 parameters (erythroid =4, neutrophils = 2, platelets = 2). Interestingly there was no correlation observed between the pretreatment TNF-α levels and hematologic response [82].

Infliximab (Remicaide) (Chimeric TNF alpha antibody)

Similar to Etanercept, Remicade has also been used in Rheumatoid arthritis (auto immune disorder) and tested in MDS. Infliximab was tried in 2 cohorts of low risk MDS with 5 and 10 mg/kg doses respectively. The drug was designed to be given every 4 weeks for a total of 4 cycles. A total of 28 patients completed 4 cycles of which 8 patients showed hematologic response while 6 patients were found to have stable disease [83]. This was followed by a randomized Phase-2 trial of Remicade in low risk MDS patients (EORTC 06023). In this study, the therapeutic efficacy of Infliximab at doses of 3 mg/k and 5 mg/kg was evaluated. A low response rate was noted with both the doses (3/22 versus 0/21 responses). Hence the study authors concluded that TNF-α blockade alone might be an insufficient therapeutic strategy in MDS.


Significant progress has been made in understanding the role of various cytokine cascades in MDS. Difficulties in stimulating normal marrow activity by conventional drugs alone provide opportunity to explore newer compounds that can alter and regulate ineffective hematopoiesis in MDS marrows. Currently P38 MAPK inhibitors, mTOR inhibitors, TGF-β pathway inhibitors, MEK inhibitors and a few other compounds are being tested in various stages of clinical development. Finding an appropriate combination of novel agents and dosing frequencies that will enhance hematologic recovery would remain a challenge that needs to be addressed in newer studies. Future studies will be aided by correlative studies of Gene mutations, aberrant DNA cytosine methylation and other genetic/epi- genetic biomarkers that will help identify a subset of MDS patients who might respond well to these new agents.



Myelodysplastic syndrome


Acute myeloid leukemia


International prognostic scoring system


International working group


Three times a day


Hematologic Improvement

HI- E:

Hematologic improvement- erythroid

HI- P:

Hematologic improvement- platelet

HI- N:

Hematologic improvement- neutrophil


Chronic myelo monocytic leukemia


Juvenile myelo monocytic leukemia


Immunoglobulin G


Transforming growth factor- β


Mitogen activated protein kinase


Mammalian target of rapamycin


Activin like kinase


Epithelial growth factor receptor

GSTP 1–1:

Glutathione S transferase pi1


Tumor necrosis factor

ON-01910 (Rigosertib):

Multi kinase inhibitor

ACE- 011:







European organization for research & treatment of cancer


Granulocyte macrophage colony stimulating factor


Granulocyte colony stimulating factor


Small hair pin ribo nucleic acid.


  1. Greenberg PL, Tuechler H, Schanz J, Sanz G, Garcia-Manero G, Sole F, Bennett JM, Bowen D, Fenaux P, Dreyfus F, Kantarjian H, Kuendgen A, Levis A, Malcovati L, Cazzola M, Cermak J, Fonatsch C, Le Beau MM, Slovak ML, Krieger O, Luebbert M, Maciejewski J, Magalhaes SM, Miyazaki Y, Pfeilstocker M, Sekeres M, Sperr WR, Stauder R, Tauro S, Valent P: Revised International Prognostic Scoring System (IPSS-R) for myelodysplastic syndromes. Blood. 2012, 10.1182/blood-2012-03-420489.

    Google Scholar 

  2. Greenberg PL: Apoptosis and its role in the myelodysplastic syndromes: implications for disease natural history and treatment. Leuk Res. 1998, 22: 1123-1136. 10.1016/S0145-2126(98)00112-X.

    Article  CAS  PubMed  Google Scholar 

  3. Mundle SD, Reza S, Ali A, Mativi Y, Shetty V, Venugopal P, Gregory SA, Raza A: Correlation of tumor necrosis factor alpha (TNF alpha) with high Caspase 3-like activity in myelodysplastic syndromes. Cancer Lett. 1999, 140: 201-207. 10.1016/S0304-3835(99)00072-5.

    Article  CAS  PubMed  Google Scholar 

  4. Zhou L, Nguyen AN, Sohal D, Ying Ma J, Pahanish P, Gundabolu K, Hayman J, Chubak A, Mo Y, Bhagat TD, Das B, Kapoun AM, Navas TA, Parmar S, Kambhampati S, Pellagatti A, Braunchweig I, Zhang Y, Wickrema A, Medicherla S, Boultwood J, Platanias LC, Higgins LS, List AF, Bitzer M, Verma A: Inhibition of the TGF-beta receptor I kinase promotes hematopoiesis in MDS. Blood. 2008, 112: 3434-3443. 10.1182/blood-2008-02-139824.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  5. Savic A, Cemerikic-Martinovic V, Dovat S, Rajic N, Urosevic I, Sekulic B, Kvrgic V, Popovic S: Angiogenesis and survival in patients with myelodysplastic syndrome. Pathol Oncol Res. 2012, 18: 681-690. 10.1007/s12253-012-9495-y.

    Article  CAS  PubMed  Google Scholar 

  6. Cunha SI, Pietras K: ALK1 as an emerging target for antiangiogenic therapy of cancer. Blood. 2011, 117: 6999-7006. 10.1182/blood-2011-01-330142.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  7. Kordasti SY, Afzali B, Lim Z, Ingram W, Hayden J, Barber L, Matthews K, Chelliah R, Guinn B, Lombardi G, Farzaneh F, Mufti GJ: IL-17-producing CD4(+) T cells, pro-inflammatory cytokines and apoptosis are increased in low risk myelodysplastic syndrome. Br J Haematol. 2009, 145: 64-72. 10.1111/j.1365-2141.2009.07593.x.

    Article  CAS  PubMed  Google Scholar 

  8. Sharma B, Altman JK, Goussetis DJ, Verma AK, Platanias LC: Protein kinase R as mediator of the effects of interferon (IFN) gamma and tumor necrosis factor (TNF) alpha on normal and dysplastic hematopoiesis. J Biol Chem. 2011, 286: 27506-27514. 10.1074/jbc.M111.238501.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  9. Furqan: Dysregulation of JAK-STAT pathway in hematological malignancies and JAK inhibitors for clinical application. Biomarker Research. 2013, 10.1186/2050-7771-1-2.

    Google Scholar 

  10. Greenberg P: Treatment of myelodysplastic syndrome with agents interfering with inhibitory cytokines. Ann Rheum Dis. 2001, 60 (Suppl 3): iii41-iii42.

    PubMed Central  CAS  PubMed  Google Scholar 

  11. Gupta D, Bachegowda L, Phadke G, Boren S, Johnson D, Misra M: Role of plasmapheresis in the management of myeloma kidney: a systematic review. Hemodial Int. 2010, 14: 355-363. 10.1111/j.1542-4758.2010.00481.x.

    Article  PubMed  Google Scholar 

  12. Newman K, Maness-Harris L, El-Hemaidi I, Akhtari M: Revisiting use of growth factors in myelodysplastic syndromes. Asian Pac J Cancer Prev. 2012, 13: 1081-1091. 10.7314/APJCP.2012.13.4.1081.

    Article  PubMed  Google Scholar 

  13. Verma A, List AF: Cytokine targets in the treatment of myelodysplastic syndromes. Curr Hematol Rep. 2005, 4: 429-435.

    CAS  PubMed  Google Scholar 

  14. Verma A, Deb DK, Sassano A, Kambhampati S, Wickrema A, Uddin S, Mohindru M, Van Besien K, Platanias LC: Cutting edge: activation of the p38 mitogen-activated protein kinase signaling pathway mediates cytokine-induced hemopoietic suppression in aplastic anemia. J Immunol. 2002, 168: 5984-5988.

    Article  CAS  PubMed  Google Scholar 

  15. Verma A, Deb DK, Sassano A, Uddin S, Varga J, Wickrema A, Platanias LC: Activation of the p38 mitogen-activated protein kinase mediates the suppressive effects of type I interferons and transforming growth factor-beta on normal hematopoiesis. J Biol Chem. 2002, 277: 7726-7735. 10.1074/jbc.M106640200.

    Article  CAS  PubMed  Google Scholar 

  16. Schmierer B, Hill CS: TGFbeta-SMAD signal transduction: molecular specificity and functional flexibility. Nat Rev Mol Cell Biol. 2007, 8: 970-982. 10.1038/nrm2297.

    Article  CAS  PubMed  Google Scholar 

  17. Navas TA, Mohindru M, Estes M, Ma JY, Sokol L, Pahanish P, Parmar S, Haghnazari E, Zhou L, Collins R, Kerr I, Nguyen AN, Xu Y, Platanias LC, List AA, Higgins LS, Verma A: Inhibition of overactivated p38 MAPK can restore hematopoiesis in myelodysplastic syndrome progenitors. Blood. 2006, 108: 4170-4177. 10.1182/blood-2006-05-023093.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  18. Sokol L, Cripe L, Kantarjian H, Sekeres MA, Parmar S, Greenberg P, Goldberg SL, Bhushan V, Shammo J, Hohl R, Verma A, Garcia-Manero G, Li YP, Lowe A, Zhu J, List AF: Randomized, dose-escalation study of the p38alpha MAPK inhibitor SCIO-469 in patients with myelodysplastic syndrome. Leukemia. 2012, 10.1038/leu.2012.264.

    Google Scholar 

  19. Keith T, Araki Y, Ohyagi M, Hasegawa M, Yamamoto K, Kurata M, Nakagawa Y, Suzuki K, Kitagawa M: Regulation of angiogenesis in the bone marrow of myelodysplastic syndromes transforming to overt leukaemia. Br J Haematol. 2007, 137: 206-215. 10.1111/j.1365-2141.2007.06539.x.

    Article  CAS  PubMed  Google Scholar 

  20. Cheng CL, Hou HA, Jhuang JY, Lin CW, Chen CY, Tang JL, Chou WC, Tseng MH, Yao M, Huang SY, Ko BS, Hsu SC, Wu SJ, Tsay W, Chen YC, Tien HF: High bone marrow angiopoietin-1 expression is an independent poor prognostic factor for survival in patients with myelodysplastic syndromes. Br J Cancer. 2011, 105: 975-982. 10.1038/bjc.2011.340.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  21. Komrokji RS: Phase 1 Dose- escalation/expansion study of the P38/Tie 2 inhibitor ARRY- 614 in patients with IPSS low-int risk MDS. 2011, ASH Abstract 118. Presented on 12/11/2011, San Diego, California

    Google Scholar 

  22. Winski SL: Role of P38 MAPK and Tie 2 in the pathogenesis of MDS and their inhibition by dual inhibitor ARRY-614. 2012, ASH Abstract 2825. Presented on 12/09/2012 at Atlanta, Georgia

    Google Scholar 

  23. Isufi I, Seetharam M, Zhou L, Sohal D, Opalinska J, Pahanish P, Verma A: Transforming growth factor-beta signaling in normal and malignant hematopoiesis. J Interferon Cytokine Res. 2007, 27: 543-552. 10.1089/jir.2007.0009.

    Article  CAS  PubMed  Google Scholar 

  24. Bhagat TD, Zhou L, Sokol L, Kessel R, Caceres G, Gundabolu K, Tamari R, Gordon S, Mantzaris I, Jodlowski T, Yu Y, Jing X, Polineni R, Bhatia K, Pellagatti A, Boultwood J, Kambhampati S, Steidl U, Stein C, Ju W, Liu G, Kenny P, List A, Bitzer M, Verma A: miR-21 mediates hematopoietic suppression in MDS by activating TGF-beta signaling. Blood. 2013, 121: 2875-2881. 10.1182/blood-2011-12-397067.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  25. Zhou L, McMahon C, Bhagat T, Alencar C, Yu Y, Fazzari M, Sohal D, Heuck C, Gundabolu K, Ng C, Mo Y, Shen W, Wickrema A, Kong G, Friedman E, Sokol L, Mantzaris I, Pellagatti A, Boultwood J, Platanias LC, Steidl U, Yan L, Yingling JM, Lahn MM, List A, Bitzer M, Verma A: Reduced SMAD7 leads to overactivation of TGF-beta signaling in MDS that can be reversed by a specific inhibitor of TGF-beta receptor I kinase. Cancer Res. 2011, 71: 955-963. 10.1158/0008-5472.CAN-10-2933.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  26. Ahnert R: First human dose (FHD) study of the oral transforming growth factor-beta receptor I kinase inhibitor LY2157299 in patients with treatment refractory malignant glioma. Clin Oncol. 2011, 29: [suppl; abstr 3011]-Chicago: ASCO 2011

    Google Scholar 

  27. Hedley BD, Allan AL, Xenocostas A: The role of erythropoietin and erythropoiesis-stimulating agents in tumor progression. Clin Cancer Res. 2011, 17: 6373-6380. 10.1158/1078-0432.CCR-10-2577.

    Article  CAS  PubMed  Google Scholar 

  28. Sibon D, Cannas G, Baracco F, Prebet T, Vey N, Banos A, Besson C, Corm S, Blanc M, Slama B, Perrier H, Fenaux P, Wattel E, Groupe Francophone des M: Lenalidomide in lower-risk myelodysplastic syndromes with karyotypes other than deletion 5q and refractory to erythropoiesis-stimulating agents. Br J Haematol. 2012, 156: 619-625. 10.1111/j.1365-2141.2011.08979.x.

    Article  CAS  PubMed  Google Scholar 

  29. Musto P, Falcone A, Sanpaolo G, Bodenizza C, La Sala A, Perla G, Carella AM: Efficacy of a single, weekly dose of recombinant erythropoietin in myelodysplastic syndromes. Br J Haematol. 2003, 122: 269-271. 10.1046/j.1365-2141.2003.04435.x.

    Article  CAS  PubMed  Google Scholar 

  30. Wang Q, Huang Z, Xue H, Jin C, Ju XL, Han JD, Chen YG: MicroRNA miR-24 inhibits erythropoiesis by targeting activin type I receptor ALK4. Blood. 2008, 111: 588-595. 10.1182/blood-2007-05-092718.

    Article  CAS  PubMed  Google Scholar 

  31. Suragani Rajashekar NVS: ACE-536, A modified type ii activin receptor increases red blood cells in vivo by promoting maturation of late stage erythroblasts. 2010, ASH Abstract 4236; Presented on 12/06/2010 at Orlando, Florida

    Google Scholar 

  32. Lin YW, Slape C, Zhang Z, Aplan PD: NUP98-HOXD13 transgenic mice develop a highly penetrant, severe myelodysplastic syndrome that progresses to acute leukemia. Blood. 2005, 106: 287-295. 10.1182/blood-2004-12-4794.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  33. Suragani RN: RAP-536 Promotes Terminal Erythroid Differentiation and Reduces Anemia in Myelodysplastic Syndromes. 2011, ASH Abstract 610; Presented at San Diego, California on 12/12/2011

    Google Scholar 

  34. Lotinun S, Pearsall RS, Davies MV, Marvell TH, Monnell TE, Ucran J, Fajardo RJ, Kumar R, Underwood KW, Seehra J, Bouxsein ML, Baron R: A soluble activin receptor Type IIA fusion protein (ACE-011) increases bone mass via a dual anabolic-antiresorptive effect in Cynomolgus monkeys. Bone. 2010, 46: 1082-1088. 10.1016/j.bone.2010.01.370.

    Article  CAS  PubMed  Google Scholar 

  35. Raje N, Vallet S: Sotatercept, a soluble activin receptor type 2A IgG-Fc fusion protein for the treatment of anemia and bone loss. Curr Opin Mol Ther. 2010, 12: 586-597.

    CAS  PubMed  Google Scholar 

  36. Chen N: Exposures and Erythropoietic Responses to Sotatercept (ACE-011) in Healthy Volunteers and Cancer Patients: Implications for Mechanism of Action. 2012, ASH Abstract 3454; Presented at Atlanta on 12/10/2012

    Google Scholar 

  37. Fan A: A Novel Nano-Immunoassay (NIA) Reveals Inhibition of PI3K and MAPK Pathways in CD34+ Bone Marrow Cells of Patients with Myelodysplastic Syndrome (MDS) Treated with the Multi-Kinase Inhibitor On 01910.Na (Rigosertib). 2011, ASH Abstract 3808; Presented at San Diego, California on 12/12/ 2011

    Google Scholar 

  38. Gumireddy K, Reddy MV, Cosenza SC, Boominathan R, Baker SJ, Papathi N, Jiang J, Holland J, Reddy EP: ON01910, a non-ATP-competitive small molecule inhibitor of Plk1, is a potent anticancer agent. Cancer Cell. 2005, 7: 275-286. 10.1016/j.ccr.2005.02.009.

    Article  CAS  PubMed  Google Scholar 

  39. Olnes MJ, Shenoy A, Weinstein B, Pfannes L, Loeliger K, Tucker Z, Tian X, Kwak M, Wilhelm F, Yong AS, Maric I, Maniar M, Scheinberg P, Groopman J, Young NS, Sloand EM: Directed therapy for patients with myelodysplastic syndromes (MDS) by suppression of cyclin D1 with ON 01910.Na. Leuk Res. 2012, 36: 982-989. 10.1016/j.leukres.2012.04.002.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  40. Raza A: Final Phase I/II Results of Rigosertib (ON 01910.Na) Hematological Effects in Patients with Myelodysplastic Syndrome and Correlation with Overall Survival. 2011, ASH Abstract 3822, Presented at San Diego, Californiaon 12/12/2011

    Google Scholar 

  41. Alvarez M, Roman E, Santos ES, Raez LE: New targets for non-small-cell lung cancer therapy. Expert Rev Anticancer Ther. 2007, 7: 1423-1437. 10.1586/14737140.7.10.1423.

    Article  CAS  PubMed  Google Scholar 

  42. Follo MY, Mongiorgi S, Bosi C, Cappellini A, Finelli C, Chiarini F, Papa V, Libra M, Martinelli G, Cocco L, Martelli AM: The Akt/mammalian target of rapamycin signal transduction pathway is activated in high-risk myelodysplastic syndromes and influences cell survival and proliferation. Cancer Res. 2007, 67: 4287-4294. 10.1158/0008-5472.CAN-06-4409.

    Article  CAS  PubMed  Google Scholar 

  43. Chen BG, Guo QY, Zhang Y, Yan WH, Pan YQ, Zheng R, Li BL, Luo WD: Effect of rapamycin on apoptosis in human myelodysplastic syndrome cell line MUTZ-1 and its possible mechanisms. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2010, 18: 300-304.

    CAS  PubMed  Google Scholar 

  44. Frost P, Shi Y, Hoang B, Lichtenstein A: AKT activity regulates the ability of mTOR inhibitors to prevent angiogenesis and VEGF expression in multiple myeloma cells. Oncogene. 2007, 26: 2255-2262. 10.1038/sj.onc.1210019.

    Article  CAS  PubMed  Google Scholar 

  45. Konrad TA, Karger A, Hackl H, Schwarzinger I, Herbacek I, Wieser R: Inducible expression of EVI1 in human myeloid cells causes phenotypes consistent with its role in myelodysplastic syndromes. J Leukoc Biol. 2009, 86: 813-822. 10.1189/jlb.0109042.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  46. Yoshimi A, Goyama S, Watanabe-Okochi N, Yoshiki Y, Nannya Y, Nitta E, Arai S, Sato T, Shimabe M, Nakagawa M, Imai Y, Kitamura T, Kurokawa M: Evi1 represses PTEN expression and activates PI3K/AKT/mTOR via interactions with polycomb proteins. Blood. 2011, 117: 3617-3628. 10.1182/blood-2009-12-261602.

    Article  CAS  PubMed  Google Scholar 

  47. Rizzieri DA, Feldman E, Dipersio JF, Gabrail N, Stock W, Strair R, Rivera VM, Albitar M, Bedrosian CL, Giles FJ: A phase 2 clinical trial of deforolimus (AP23573, MK-8669), a novel mammalian target of rapamycin inhibitor, in patients with relapsed or refractory hematologic malignancies. Clin Cancer Res. 2008, 14: 2756-2762. 10.1158/1078-0432.CCR-07-1372.

    Article  CAS  PubMed  Google Scholar 

  48. Janakiram M, Thirukonda VK, Sullivan M, Petrich AM: Emerging Therapeutic Targets in Diffuse Large B-Cell Lymphoma. Curr Treat Options Oncol. 2012, 10.1007/s11864-011-0178-9.

    Google Scholar 

  49. Xu C, Zhou Q, Wu YL: Can EGFR-TKIs be used in first line treatment for advanced non-small cell lung cancer based on selection according to clinical factors? - A literature-based meta-analysis. J Hematol Oncol. 2012, 5: 62-10.1186/1756-8722-5-62.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  50. Alexander C, Scot R, William T: EGFR inhibition in non-small cell lung cancer: current evidence and future directions. Bio Marker Research. 2013, 10.1186/2050-7771-1-2.

    Google Scholar 

  51. Stegmaier K, Corsello SM, Ross KN, Wong JS, Deangelo DJ, Golub TR: Gefitinib induces myeloid differentiation of acute myeloid leukemia. Blood. 2005, 106: 2841-2848. 10.1182/blood-2005-02-0488.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  52. Boehrer S: Increased Proliferation Induced by Constitutive Activation of the Src-Kinase Lyn and Aberrant mTOR Signaling in AML Is Abrogated by the EGFR-Inhibitor Erlotinib. 2009, ASH Abstract 3813;Presented at New Orleans on 12/07 2009

    Google Scholar 

  53. Boehrer S, Ades L, Braun T, Galluzzi L, Grosjean J, Fabre C, Le Roux G, Gardin C, Martin A, de Botton S, Fenaux P, Kroemer G: Erlotinib exhibits antineoplastic off-target effects in AML and MDS: a preclinical study. Blood. 2008, 111: 2170-2180. 10.1182/blood-2007-07-100362.

    Article  CAS  PubMed  Google Scholar 

  54. Komrokji RS: Erlotinib for Treatment of Myelodysplastic Syndromes: A phase II clinical study. 2010, ASH Abstract 1854. Presented at Orlando, Florida on 12/4/2010

    Google Scholar 

  55. Lainey E: Potentiation of Apoptosis in MDS/AML by Combination of Azacitidine and the EGFR-Tyrosine Kinase Inhibitor (TKI) Erlotinib. 2011, ASH Abstract 2790. Presented at San Diego, California on 12/11/2011

    Google Scholar 

  56. Lainey E: Erlotinib Antagonizes Efflux Via ABC Transporters and Decreases P-Gp Cell Surface Expression by Inhibiting SRC Kinase and mTOR Pathways in Acute Myeloid Leukemia (AML). 2011, ASH Abstract 2564; Presented at San Diego on 12/11/2011

    Google Scholar 

  57. Adler V, Yin Z, Fuchs SY, Benezra M, Rosario L, Tew KD, Pincus MR, Sardana M, Henderson CJ, Wolf CR, Davis RJ, Ronai Z: Regulation of JNK signaling by GSTp. EMBO J. 1999, 18: 1321-1334. 10.1093/emboj/18.5.1321.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  58. Galili N, Tamayo P, Botvinnik OB, Mesirov JP, Brooks MR, Brown G, Raza A: Prediction of response to therapy with ezatiostat in lower risk myelodysplastic syndrome. J Hematol Oncol. 2012, 5: 20-10.1186/1756-8722-5-20.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  59. Raza A, Galili N, Smith SE, Godwin J, Boccia RV, Myint H, Mahadevan D, Mulford D, Rarick M, Brown GL, Schaar D, Faderl S, Komrokji RS, List AF, Sekeres M: A phase 2 randomized multicenter study of 2 extended dosing schedules of oral ezatiostat in low to intermediate-1 risk myelodysplastic syndrome. Cancer. 2012, 118: 2138-2147. 10.1002/cncr.26469.

    Article  CAS  PubMed  Google Scholar 

  60. Raza A, Galili N, Callander N, Ochoa L, Piro L, Emanuel P, Williams S, Burris H, Faderl S, Estrov Z, Curtin P, Larson RA, Keck JG, Jones M, Meng L, Brown GL: Phase 1-2a multicenter dose-escalation study of ezatiostat hydrochloride liposomes for injection (Telintra, TLK199), a novel glutathione analog prodrug in patients with myelodysplastic syndrome. J Hematol Oncol. 2009, 2: 20-10.1186/1756-8722-2-20.

    Article  PubMed Central  PubMed  Google Scholar 

  61. Raza A, Galili N, Mulford D, Smith SE, Brown GL, Steensma DP, Lyons RM, Boccia R, Sekeres MA, Garcia-Manero G, Mesa RA: Phase 1 dose-ranging study of ezatiostat hydrochloride in combination with lenalidomide in patients with non-deletion (5q) low to intermediate-1 risk myelodysplastic syndrome (MDS). J Hematol Oncol. 2012, 5: 18-10.1186/1756-8722-5-18.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  62. Repasky GA, Chenette EJ, Der CJ: Renewing the conspiracy theory debate: does Raf function alone to mediate Ras oncogenesis?. Trends Cell Biol. 2004, 14: 639-647. 10.1016/j.tcb.2004.09.014.

    Article  CAS  PubMed  Google Scholar 

  63. Reuter CW, Morgan MA, Bergmann L: Targeting the Ras signaling pathway: a rational, mechanism-based treatment for hematologic malignancies?. Blood. 2000, 96: 1655-1669.

    CAS  PubMed  Google Scholar 

  64. Appels NM, Beijnen JH, Schellens JH: Development of farnesyl transferase inhibitors: a review. Oncologist. 2005, 10: 565-578. 10.1634/theoncologist.10-8-565.

    Article  PubMed  Google Scholar 

  65. Rowinsky EK, Windle JJ, Von Hoff DD: Ras protein farnesyltransferase: A strategic target for anticancer therapeutic development. J Clin Oncol. 1999, 17: 3631-3652.

    CAS  PubMed  Google Scholar 

  66. End DW, Smets G, Todd AV, Applegate TL, Fuery CJ, Angibaud P, Venet M, Sanz G, Poignet H, Skrzat S, Devine A, Wouters W, Bowden C: Characterization of the antitumor effects of the selective farnesyl protein transferase inhibitor R115777 in vivo and in vitro. Cancer Res. 2001, 61: 131-137.

    CAS  PubMed  Google Scholar 

  67. Kurzrock R, Kantarjian HM, Cortes JE, Singhania N, Thomas DA, Wilson EF, Wright JJ, Freireich EJ, Talpaz M, Sebti SM: Farnesyltransferase inhibitor R115777 in myelodysplastic syndrome: clinical and biologic activities in the phase 1 setting. Blood. 2003, 102: 4527-4534. 10.1182/blood-2002-11-3359.

    Article  CAS  PubMed  Google Scholar 

  68. Kurzrock R, Albitar M, Cortes JE, Estey EH, Faderl SH, Garcia-Manero G, Thomas DA, Giles FJ, Ryback ME, Thibault A, De Porre P, Kantarjian HM: Phase II study of R115777, a farnesyl transferase inhibitor, in myelodysplastic syndrome. J Clin Oncol. 2004, 22: 1287-1292. 10.1200/JCO.2004.08.082.

    Article  CAS  PubMed  Google Scholar 

  69. Fenaux P, Raza A, Mufti GJ, Aul C, Germing U, Kantarjian H, Cripe L, Kerstens R, De Porre P, Kurzrock R: A multicenter phase 2 study of the farnesyltransferase inhibitor tipifarnib in intermediate- to high-risk myelodysplastic syndrome. Blood. 2007, 109: 4158-4163. 10.1182/blood-2006-07-035725.

    Article  CAS  PubMed  Google Scholar 

  70. Feldman EJ, Cortes J, DeAngelo DJ, Holyoake T, Simonsson B, O'Brien SG, Reiffers J, Turner AR, Roboz GJ, Lipton JH, Maloisel F, Colombat P, Martinelli G, Nielsen JL, Petersdorf S, Guilhot F, Barker J, Kirschmeier P, Frank E, Statkevich P, Zhu Y, Loechner S, List A: On the use of lonafarnib in myelodysplastic syndrome and chronic myelomonocytic leukemia. Leukemia. 2008, 22: 1707-1711. 10.1038/leu.2008.156.

    Article  CAS  PubMed  Google Scholar 

  71. Ravoet C, Mineur P, Robin V, Debusscher L, Bosly A, Andre M, El Housni H, Soree A, Bron D, Martiat P: Farnesyl transferase inhibitor (lonafarnib) in patients with myelodysplastic syndrome or secondary acute myeloid leukaemia: a phase II study. Ann Hematol. 2008, 87: 881-885. 10.1007/s00277-008-0536-2.

    Article  CAS  PubMed  Google Scholar 

  72. Messersmith WA, Hidalgo M, Carducci M, Eckhardt SG: Novel targets in solid tumors: MEK inhibitors. Clin Adv Hematol Oncol. 2006, 4: 831-836.

    PubMed  Google Scholar 

  73. McCubrey JA, Steelman LS, Abrams SL, Bertrand FE, Ludwig DE, Basecke J, Libra M, Stivala F, Milella M, Tafuri A, Lunghi P, Bonati A, Martelli AM: Targeting survival cascades induced by activation of Ras/Raf/MEK/ERK, PI3K/PTEN/Akt/mTOR and Jak/STAT pathways for effective leukemia therapy. Leukemia. 2008, 22: 708-722. 10.1038/leu.2008.27.

    Article  CAS  PubMed  Google Scholar 

  74. Sebolt-Leopold JS: MEK inhibitors: a therapeutic approach to targeting the Ras-MAP kinase pathway in tumors. Curr Pharm Des. 2004, 10: 1907-1914. 10.2174/1381612043384439.

    Article  CAS  PubMed  Google Scholar 

  75. Mueller H, Flury N, Eppenberger-Castori S, Kueng W, David F, Eppenberger U: Potential prognostic value of mitogen-activated protein kinase activity for disease-free survival of primary breast cancer patients. Int J Cancer. 2000, 89: 384-388. 10.1002/1097-0215(20000720)89:4<384::AID-IJC11>3.0.CO;2-R.

    Article  CAS  PubMed  Google Scholar 

  76. Milella M, Kornblau SM, Estrov Z, Carter BZ, Lapillonne H, Harris D, Konopleva M, Zhao S, Estey E, Andreeff M: Therapeutic targeting of the MEK/MAPK signal transduction module in acute myeloid leukemia. J Clin Invest. 2001, 108: 851-859.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  77. Milella M, Konopleva M, Precupanu CM, Tabe Y, Ricciardi MR, Gregorj C, Collins SJ, Carter BZ, D'Angelo C, Petrucci MT, Foa R, Cognetti F, Tafuri A, Andreeff M: MEK blockade converts AML differentiating response to retinoids into extensive apoptosis. Blood. 2007, 109: 2121-2129. 10.1182/blood-2006-05-024679.

    Article  CAS  PubMed  Google Scholar 

  78. Lyubynska N, Gorman MF, Lauchle JO, Hong WX, Akutagawa JK, Shannon K, Braun BS: A MEK inhibitor abrogates myeloproliferative disease in Kras mutant mice. Sci Transl Med. 2011, 3: 76ra27-10.1126/scitranslmed.3001069.

    Article  PubMed Central  PubMed  Google Scholar 

  79. Borthakur GLP, Kirschbaum MH, Foran JM, Kadia TM, Jabbour E, Boyiadzis M, Verma A: Phase I/II trial of the MEK1/2 inhibitor GSK1120212 (GSK212) in patients (pts) with relapsed/refractory myeloid malignancies: Evidence of activity in pts with RAS mutation. 2011, ASCO abstract 6506, presented at ASCO 2011 meeting, Chicago

    Google Scholar 

  80. Feldmann M, Maini RN: Anti-TNF alpha therapy of rheumatoid arthritis: what have we learned?. Annu Rev Immunol. 2001, 19: 163-196. 10.1146/annurev.immunol.19.1.163.

    Article  CAS  PubMed  Google Scholar 

  81. Molnar L, Berki T, Hussain A, Nemeth P, Losonczy H: Detection of TNFalpha expression in the bone marrow and determination of TNFalpha production of peripheral blood mononuclear cells in myelodysplastic syndrome. Pathol Oncol Res. 2000, 6: 18-23. 10.1007/BF03032653.

    Article  CAS  PubMed  Google Scholar 

  82. Deeg HJ, Gotlib J, Beckham C, Dugan K, Holmberg L, Schubert M, Appelbaum F, Greenberg P: Soluble TNF receptor fusion protein (etanercept) for the treatment of myelodysplastic syndrome: a pilot study. Leukemia. 2002, 16: 162-164. 10.1038/sj.leu.2402356.

    Article  CAS  PubMed  Google Scholar 

  83. Raza A, Candoni A, Khan U, Lisak L, Tahir S, Silvestri F, Billmeier J, Alvi MI, Mumtaz M, Gezer S, Venugopal P, Reddy P, Galili N: Remicade as TNF suppressor in patients with myelodysplastic syndromes. Leuk Lymphoma. 2004, 45: 2099-2104. 10.1080/10428190410001723322.

    Article  CAS  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations


Corresponding author

Correspondence to Amit Verma.

Additional information

Competing interests

The authors declare that they have no competing interest.

Authors’ contributions

LB – Was responsible for reviewing literature, write up of Manuscript and proof- reading, OG- Responsible for Figures and proof reading, AV- Designed the review, expert opinion & proof reading, Others- Corroborate with literature, proof reading and editorial responsibilities. All authors read and approved the final manuscript.

Authors’ original submitted files for images

Rights and permissions

Open Access This article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution License ( ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Reprints and permissions

About this article

Cite this article

Bachegowda, L., Gligich, O., Mantzaris, I. et al. Signal transduction inhibitors in treatment of myelodysplastic syndromes. J Hematol Oncol 6, 50 (2013).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: