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GNA15 as a potential prognostic and immunological biomarker in ccRCC based on bioinformatics analysis and

Xiumin Xu1, Zeping Zuo2, Jinhai Zhu2

  • 1Department of Urology, The Second Affiliated Hospital of Anhui Medical University, Hefei, Anhui, 230601, China; Department of Urology, Tongling People's Hospital, Tongling, Anhui, 244000, China.

Experimental Cell Research
|December 26, 2025
PubMed
Summary

GNA15 is highly expressed in clear cell renal cell carcinoma (ccRCC), promoting tumor growth and immune suppression. Targeting GNA15 may offer a new therapeutic strategy for this aggressive kidney cancer.

Keywords:
Cancer stemnessGNA15ImmunotherapyTumor microenvironmentccRCC

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Area of Science:

  • Oncology
  • Molecular Biology
  • Immunology

Background:

  • Clear cell renal cell carcinoma (ccRCC) is an aggressive kidney cancer subtype with limited treatment options.
  • The role of GNA15, a G protein alpha subunit, in ccRCC progression is not well understood.

Purpose of the Study:

  • To investigate the expression, function, and clinical significance of GNA15 in ccRCC.
  • To explore GNA15 as a potential prognostic biomarker and therapeutic target for ccRCC.

Main Methods:

  • Analysis of public datasets for GNA15 expression and correlation with clinical data.
  • Validation of GNA15 levels in ccRCC tissues and cell lines using immunofluorescence and western blotting.
  • Functional assays (e.g., migration, proliferation) and gene set enrichment analysis (GSEA) after GNA15 knockdown.

Main Results:

  • GNA15 is upregulated in ccRCC and associated with poor prognosis, advanced stage, tumor heterogeneity, and stemness.
  • High GNA15 expression correlates with an immunosuppressive microenvironment, including M2 macrophage and neutrophil infiltration.
  • GNA15 knockdown inhibits ccRCC cell proliferation, migration, and stemness marker expression, and reduces PD-L1 levels.

Conclusions:

  • GNA15 is a novel oncogenic factor and immune modulator contributing to ccRCC progression.
  • GNA15 represents a promising prognostic biomarker and therapeutic target for ccRCC.