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  • mProX™ Human FGL1 Stable Cell Line

    [CAT#: S01YF-1023-PY269]
    Product Category:
    Membrane Protein Stable Cell Lines
    Subcategory:

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    Product Information

    Target Family
    Other Targets
    Target Protein Species
    Human
    Host Cell Type
    HEK293;CHO-K1;PC-9
    Target Classification
    Other Targets Drug Discovery Assays and Products
    Target Research Area
    Cancer Research
    Related Diseases
    Hepatocellular Carcinoma; Lung Cancer
    Gene ID
    Human:2267
    UniProt ID
    Human:Q08830

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    FGL1, or fibrinogen-like protein 1, has been found to play a role in immune escape and progression of metastatic colorectal cancer. It is secreted by cancer cells and hepatocytes and reduces the infiltration of T cells. FGL1 stability is enhanced by the TAM-OTUD1-FGL1 axis, which is activated by tumor-associated macrophages (TAMs) in the liver microenvironment. Disrupting this axis inhibits tumor progression and synergizes with immune checkpoint blockade therapy. High plasma FGL1 levels predict poor outcomes and reduced benefits from immunotherapy. Additionally, FGL1 has been found to be highly expressed in head and neck squamous cell carcinoma (HNSCC) and promotes the malignant progression of HNSCC cells. In non-small cell lung cancer (NSCLC), various chemotherapeutic drugs have been shown to upregulate the expression of immune checkpoint ligands, including PD-L1 and PD-L2, which may impact the efficacy of combined immunotherapy.

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    FAQ

    chat Morgan Jones (Verified Customer)

    How does FGL1 interact with the immune system in cancer? Jun 10 2023

    chat Patrick Liam (Creative Biolabs Scientific Support)

    FGL1 plays a role in tumor epithelial to mesenchymal transition and immune escape, suggesting its involvement in modulating the immune response in cancer. Jun 10 2023

    chat Peyton Johnson (Verified Customer)

    Can FGL1 be used as a diagnostic marker for hepatocellular carcinoma? Nov 01 2022

    chat Patrick Liam (Creative Biolabs Scientific Support)

    Serum FGL1 levels are significantly elevated in patients with HBV-related hepatocellular carcinoma, indicating its potential as a diagnostic marker. Nov 01 2022

    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

    Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR CLINICAL PROCEDURES" For licensing inquiries, please contact
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