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  • mProX™ Human GPC3 Stable Cell Line

    [CAT#: S01YF-1023-PY273]
    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;Huh-7
    Target Classification
    Other Targets Drug Discovery Assays and Products
    Target Research Area
    Cancer Research
    Related Diseases
    Simpson-Golabi-Behmel Syndrome, Type 1; Wilms Tumor 1
    Gene ID
    Human:2719
    UniProt ID
    Human:P51654

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    Glypican-3 (GPC3) is a heparan sulfate proteoglycan that has been extensively studied for its role in hepatocellular carcinoma (HCC). Its overexpression in HCC makes it a potential diagnostic and therapeutic target. Recent advancements have led to the development of GPC3-targeted immunoPET imaging strategies, offering superior diagnostic accuracies in preclinical HCC models. Furthermore, the modulation of the GPC3 pathway has shown promise in overcoming drug resistance in HCC, highlighting its significance in therapeutic interventions.

    Protocols

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    FAQ

    chat Morgan Johnson (Verified Customer)

    Is GPC3 a potential therapeutic target for small cell lung cancer (SCLC)? Oct 26 2020

    chat Patrick Liam (Creative Biolabs Scientific Support)

    GPC3 has been identified as a potential therapeutic target for SCLC, with recombinant immunotoxins targeting GPC3 showing cytotoxicity to SCLC cells. Oct 26 2020

    chat Skyler Garcia (Verified Customer)

    Can GPC3 be used for imaging and therapy of hepatocellular carcinoma? Jun 16 2022

    chat Patrick Liam (Creative Biolabs Scientific Support)

    GPC3-targeted imaging and therapeutic strategies, such as immunoPET imaging and nanocarrier-based drug delivery, have shown promise in the detection and treatment of hepatocellular carcinoma expressing GPC3. Jun 16 2022

    Published Data

    Fig.1 Knockdown of GPC3 in Huh-7 cells.

    The expression of GPC3 in Huh7 cells was assessed through Western blot analysis, with experiments being conducted in triplicate, and the results were expressed as mean values, demonstrating a significant difference (P < 0.01) compared to the control, while GAPDH was utilized as a loading control.

    Ref: Miao, Hui-Lai, et al. "Knockdown of GPC3 inhibits the proliferation of Huh7 hepatocellular carcinoma cells through down-regulation of YAP." Journal of cellular biochemistry 114.3 (2013): 625-631.

    Pubmed: 23060277

    DOI: 10.1002/jcb.24404

    Research Highlights

    Lu, Li-Li. et al. "GPC3-IL7-CCL19-CAR-T primes immune microenvironment reconstitution for hepatocellular carcinoma therapy." Cell biology and toxicology, 2023.
    The present study examines the efficacy of GPC3-7-19-CAR-T cells, a novel chimeric antigen receptor (CAR)-T-cell therapy developed by the authors, in treating advanced hepatocellular carcinoma (HCC). Conventional GPC3-CAR-T cells have shown unsatisfactory clinical results in HCC, and the underlying mechanism remains unclear. The authors aim to elucidate the clinical potential of GPC3-7-19-CAR-T cells and investigate the mechanisms behind their antitumor effects. This innovative approach has the potential to significantly impact the treatment of advanced cancer.
    Lu, Li-Li. et al. "GPC3-IL7-CCL19-CAR-T primes immune microenvironment reconstitution for hepatocellular carcinoma therapy." Cell biology and toxicology, 2023.
    Pubmed: 37853185   DOI: 10.1007/s10565-023-09821-w

    Tavakoli Pirzaman, Ali. et al. "The Role of microRNAs in Regulating Cancer Cell Response to Oxaliplatin-Containing Regimens." Technology in cancer research & treatment, 2023.
    Oxaliplatin (cyclohexane-1,2-diamine; oxalate; platinum [2+]) is a third-generation chemotherapeutic drug with potent anticancer properties. It has been used in the treatment of various types of cancer, including colorectal cancer, breast cancer, lung cancer, bladder cancer, prostate cancer, and gastric cancer. However, despite its efficacy, the development of resistance to oxaliplatin poses a challenge in its therapeutic utility. This review examined the role of microRNAs, a subtype of small non-coding RNAs, in modulating oxaliplatin's response in gastrointestinal cancers. Furthermore, it discussed the potential of microRNA-based strategies in enhancing the sensitivity of cancer cells to oxaliplatin and reducing oxaliplatin-induced neuropathic pain.
    Tavakoli Pirzaman, Ali. et al. "The Role of microRNAs in Regulating Cancer Cell Response to Oxaliplatin-Containing Regimens." Technology in cancer research & treatment, 2023.
    Pubmed: 37849311   DOI: 10.1177/15330338231206003

    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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