From: Fibrinogen-like protein 1 (FGL1): the next immune checkpoint target
No | Year | Tumor type | Numbers/samples | FGL1 detection methods | Conclusions | References |
---|---|---|---|---|---|---|
1 | 2020 | BC | N = 47, primary tumor tissue; N = 82, peripheral blood | IHC; flow cytometry | FGL1 was present and tended to be expressed at higher levels in stage III cancer cells than in stage I or II cancer cells | [163] |
2 | 2020 | HCC | N = 143, primary tumor tissue | Multiplex IF | High FGL1 expression was negatively associated with PD-L1 expression and the CD8+ T cell density but positively associated with high LAG3+ T cell density | [165] |
3 | 2019 | LUAD | N = 30, primary tumor tissue | IHC | Low FGL1 expression contributed to EMT and angiogenesis in LKB1-low LUAD tissue samples | [93] |
4 | 2019 | NSCLC | N = 275, plasma | Multiplex QIF | FGL1 was shown to exhibit a relatively high expression level in tumor cells compared with the stromal distribution and paired normal tissues; ~ 15% NSCLC patients showed elevated expression, implying a worse 5-year OS rate | [50] |
 |  |  | N = 74, plasma | ELISA | Higher plasma FGL1 levels were detected in NSCLC patients than in healthy donors; the plasma FGL1 levels in NSCLC patients were not associated with tumor metastasis or liver injury |  |
 |  |  | N = 18, plasma | ELISA | Higher plasma FGL1 levels were associated with worse OS in NSCLC patients treated with anti-PD-1/PD-L1 therapy |  |
5 | 2019 | MM | N = 21, plasma | ELISA | Higher plasma FGL1 levels were associated with worse OS in metastatic melanoma patients treated with anti-PD-1/PD-L1 therapy |  |
6 | 2019 | GC | N = 50, primary tumor tissue | qPCR and WB | Both the mRNA and protein levels of FGL1 were obviously higher in GC tissues than in normal tissues (P < 0.001); high FGL1 expression was related to a poor prognosis (P < 0.01); the FGL1 expression, pathological stage and histological grade were positively associated with the OS of GC patients (P < 0.05) | [94] |