Evidence map›Paper›PMID 42729068›Full record

ArticleTranslational andrology and urology2026

Bioinformatics analysis and experimental validation confirm COL6A3 as a promising target for renal cell carcinoma therapy.

Zheng Qin, Xiepeng Zuo, Yueyao Zhang, Dongze Liu, Shengnan Yin, Kaibin Wang, Xiao Zhu, Yuanhao Zhang, Kexin Xu, Xiaoping Cai and 2 more

Abstract read
In one paragraph

Article in Translational andrology and urology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

12 authors.

Zheng Qin *Tianjin Key Laboratory of Precision Medicine for Sex Hormones and Diseases, The Second Hospital of Tianjin Medical University, Tianjin, China.
Xiepeng Zuo *Department of Urology, The First Hospital of Hebei Medical University, Shijiazhuang, China.
Yueyao Zhang *Department of Cell Biology, Peking University Cancer Hospital & Institute, Beijing, China.
Dongze Liu *Department of Urology, The Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Shengnan Yin *Department of Urology, The First Hospital of Hebei Medical University, Shijiazhuang, China.
Kaibin WangTianjin Key Laboratory of Precision Medicine for Sex Hormones and Diseases, The Second Hospital of Tianjin Medical University, Tianjin, China.
Xiao ZhuTianjin Key Laboratory of Precision Medicine for Sex Hormones and Diseases, The Second Hospital of Tianjin Medical University, Tianjin, China.
Yuanhao ZhangTianjin Key Laboratory of Precision Medicine for Sex Hormones and Diseases, The Second Hospital of Tianjin Medical University, Tianjin, China.
Kexin XuTianjin Key Laboratory of Precision Medicine for Sex Hormones and Diseases, The Second Hospital of Tianjin Medical University, Tianjin, China.
Xiaoping CaiDepartment of Urology, The First Hospital of Hebei Medical University, Shijiazhuang, China.
Xiaowei WangDepartment of Urology, The First Hospital of Hebei Medical University, Shijiazhuang, China.
Shuo ZhengDepartment of Urology, The First Hospital of Hebei Medical University, Shijiazhuang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Kidney cancer is a prevalent urogenital malignancy, with renal cell carcinoma (RCC) accounting for over 90% of cases. Despite the rising incidence and the primary use of surgery as a treatment, mortality rates remain high, highlighting an urgent need for effective therapeutic strategies. Collagen VI alpha 3 (COL6A3), an isoform of collagen VI, is known to play a key role in the pathogenesis of diabetes and obesity. However, its expression pattern, clinicopathological features, prognostic significance, and immune-related associations in RCC remain largely unexplored. Therefore, the aim of this study is to elucidate the biological function of COL6A3 in RCC, specifically exploring its role in the tumor immune microenvironment and the PI3K-AKT signaling pathway, to identify a novel therapeutic target. Methods: We investigated COL6A3 expression and associated clinical outcomes using online databases, including Tumor Immune Estimation Resource (TIMER), Gene Expression Profiling Interactive Analysis 2 (GEPIA2), and University of Alabama at Birmingham Cancer Data Analysis Portal (UALCAN), along with multiple R packages. Furthermore, tumor immune infiltration and immunotherapeutic responses, and chemotherapeutic sensitivities were computationally evaluated. Subsequently, biological functions were validated using Western blot, quantitative real-time polymerase chain reaction (qRT-PCR), immunohistochemistry (IHC), Cell Counting Kit-8 (CCK-8), colony formation, 5-ethynyl-2'-deoxyuridine (EdU), wound healing, and Transwell assays, and Results: Our analysis revealed that COL6A3 expression was significantly upregulated in RCC tissues. High COL6A3 expression correlated with poor clinical prognosis and malignant progression. Conclusions: These findings indicate that COL6A3 acts as an oncogenic driver and a potential immunosuppressive indicator, serving as a novel prognostic biomarker and therapeutic target. This dual role offers new insights for stratifying patients and developing tailored immunotherapeutic and targeted therapies for renal cancer.

Indexed as

accurate treatmentanti-cancerbiomarker for immunotherapydiagnostic and prognostic biomarkersRenal cell carcinoma (RCC)

Identifiers

PMID42729068
PMCPMC13561743

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