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  • mProX™ Human CCDC6 Stable Cell Line

    [CAT#: S01YF-1023-PY81]
    Product Category:
    Membrane Protein Stable Cell Lines
    Subcategory:
    Kinase Cell Lines

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    Product Information

    Target Family
    Kinases/Enzyme
    Target Protein Species
    Human
    Host Cell Type
    HEK293;CHO-K1;HCT116
    Target Classification
    Kinase Cell Lines
    Target Research Area
    Cancer Research
    Related Diseases
    Differentiated Thyroid Carcinoma; Papillary Carcinoma
    Gene ID
    Human:8030
    UniProt ID
    Human:Q16204

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    CCDC6 is a gene that is involved in various types of cancer, including thyroid cancer, colorectal carcinoma, sweat gland tumors, and pancreatic ductal adenocarcinoma. In thyroid cancer, CCDC6-RET fusions are associated with concurrent molecular alterations and potentially aggressive features. In colorectal carcinoma, CCDC6 is one of the fusion partners of RET, and RET fusion positive colorectal carcinoma may be a unique molecular subset. In sweat gland tumors, CCDC6-RET fusion transcripts have been identified in cystadenoma/hidrocystoma-like tumors. In pancreatic ductal adenocarcinoma, CCDC6 is one of the genetic alterations observed, along with other common drivers such as KRAS, TP53, and SMAD4. The presence of CCDC6 alterations in these different types of cancer suggests its potential role as a diagnostic and prognostic marker, as well as a potential target for personalized treatment approaches.

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    FAQ

    chat Skyler Smith (Verified Customer)

    How does CCDC6 affect ovarian carcinoma response to PARP inhibitors? Dec 13 2021

    chat Patrick Liam (Creative Biolabs Scientific Support)

    Disruption of the CCDC6-PP4 axis induces a BRCAness-like phenotype, enhancing sensitivity to PARP inhibitors in high-grade serous ovarian carcinoma. Dec 13 2021

    chat Taylor Williams (Verified Customer)

    Is CCDC6 expression related to prognosis in hepatobiliary carcinoma? Sep 08 2021

    chat Patrick Liam (Creative Biolabs Scientific Support)

    High expression of CCDC6 is associated with unfavorable outcomes and immune cell infiltration in hepatobiliary carcinoma, suggesting its potential as a predictive biomarker. Sep 08 2021

    Published Data

    Fig.1 In vitro, An increase in cell death were observed as a consequence of CCDC6 knockdown.

    Ref: Thanasopoulou, Angeliki, et al. "Loss of CCDC6 affects cell cycle through impaired intra-S-phase checkpoint control." PloS one 7.2 (2012): e31007.

    Pubmed: 22363533

    DOI: 10.1371/journal.pone.0031007

    Research Highlights

    Zhou, Yuanyuan. et al. "Performance of multigene testing in cytologically indeterminate thyroid nodules and molecular risk stratification." PeerJ, 2023.
    Thyroid cancer ranks as the third most common form of cancer in women, creating a pressing need for improved diagnostic methods. To address this, researchers crafted a custom multigene testing panel and assessed its effectiveness in 529 thyroid nodules with uncertain cytological findings (Bethesda III, IV, and V). By analyzing molecular data from fine needle aspiration samples alongside clinical diagnoses and surgical outcomes, the study aimed to enhance the accuracy of malignancy prediction. The findings demonstrated a substantial overall agreement (Kappa = 0.726) with 97.80% sensitivity, 82.14% specificity, 98.99% positive predictive value, and 67.65% negative predictive value. Notably, the study identified prevalent genetic abnormalities, such as BRAFV600E (82.59%) and NRAS mutants (4.07%). Additionally, the research revealed potential links between certain molecular alterations and aggressive tumor characteristics. Ultimately, this investigation presented a valuable multigene panel for distinguishing benign from uncertain thyroid nodules, reducing unnecessary surgeries, and highlighted the potential of molecular risk stratification in predicting disease outcomes, while acknowledging the study's limitations due to the cohort's high cancer prevalence.
    Zhou, Yuanyuan. et al. "Performance of multigene testing in cytologically indeterminate thyroid nodules and molecular risk stratification." PeerJ, 2023.
    Pubmed: 37744220   DOI: 10.7717/peerj.16054

    Nagasaka, Misako. et al. "Pan-tumor survey of RET fusions as detected by next-generation RNA sequencing identified RET fusion positive colorectal carcinoma as a unique molecular subset." Translational oncology, 2023.
    RET fusions are considered driver alterations in cancer, which are often observed in non-small cell lung cancer and well-differentiated thyroid cancer. Though primarily seen in these two types of cancer, reports have also shown the presence of RET fusions in other solid tumors. This prominent genetic anomaly has been linked to tumor progression and is therefore a crucial target for therapeutic strategies. Further research on the role of RET fusion in various types of cancer may uncover potential treatment options. Within this context, RET fusion detection and management could potentially lead to improved clinical outcomes for these patients.
    Nagasaka, Misako. et al. "Pan-tumor survey of RET fusions as detected by next-generation RNA sequencing identified RET fusion positive colorectal carcinoma as a unique molecular subset." Translational oncology, 2023.
    Pubmed: 37516008   DOI: 10.1016/j.tranon.2023.101744

    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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