mProX™ Human FGL1 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
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Published Data
Fig.1 Knockdown of FGL1 in PC9/GR cells.
The western blotting method was employed to measure the relative expression of FGL1 protein in PC9/GR cells after interference with FGL1, revealing alterations in FGL1 protein levels.
Ref: Sun, Cuilan, et al. "FGL1 regulates acquired resistance to Gefitinib by inhibiting apoptosis in non-small cell lung cancer." Respiratory research 21 (2020): 1-11.
Pubmed: 32778129
DOI: 10.1186/s12931-020-01477-y
Research Highlights
Pan, Zhiyong. et al. "Increased FGL1 Expression Predicts Poor Prognosis and Promotes EMT in Head and Neck Squamous Cell Carcinoma." Biochemical genetics, 2023.
Fibrinogen-like protein 1 (FGL1) is secreted by the liver and plays a role in proliferation and metabolism. It is often abnormally expressed in human malignancies, but its role in head and neck squamous cell carcinoma (HNSCC) is not well-understood. In this study, the authors analyzed FGL1 expression in HNSCC using the TCGA database and observed its impact on patient survival. They also conducted cell-based and in vivo experiments to investigate the role of FGL1 in HNSCC. Results showed that FGL1 was highly expressed in HNSCC and correlated with a poor prognosis. Knockdown of FGL1 inhibited the proliferation and invasion of HNSCC cells, and mechanistic analysis revealed that FGL1 induced an epithelial-mesenchymal transition (EMT) phenotype, promoting the malignant progression of HNSCC. In summary, the authors' findings suggest that FGL1, an oncogene, may represent a potential therapeutic target for HNSCC treatment.
Pan, Zhiyong. et al. "Increased FGL1 Expression Predicts Poor Prognosis and Promotes EMT in Head and Neck Squamous Cell Carcinoma." Biochemical genetics, 2023.
Pubmed:
37843652
DOI:
10.1007/s10528-023-10545-z
Garman, Bradley. et al. "Comprehensive immunophenotyping of solid tumor-infiltrating immune cells reveals the expression characteristics of LAG-3 and its ligands." Frontiers in immunology, 2023.
The critical role of immune cell expression profiling from patient samples in the development of successful immuno-oncology agents cannot be understated. Understanding the mechanism-of-action, identifying predictive exploratory biomarkers, and guiding treatment selection and combination therapy strategies are all made possible through this profiling. Recently, clinical success has been demonstrated by targeting LAG-3, an inhibitory immune checkpoint that suppresses antitumor T-cell responses, in combination with PD-1. In this study, the authors aimed to identify human immune cell subsets expressing LAG-3 and its ligands, characterize their marker expression profiles, and investigate any potential correlation with clinical outcomes of immuno-oncology therapies.
Garman, Bradley. et al. "Comprehensive immunophenotyping of solid tumor-infiltrating immune cells reveals the expression characteristics of LAG-3 and its ligands." Frontiers in immunology, 2023.
Pubmed:
37795090
DOI:
10.3389/fimmu.2023.1151748