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Updated: Jan 6, 2026

Impedance-based Real-time Measurement of Cancer Cell Migration and Invasion
Published on: April 2, 2020
Integrative analysis reveals CRHBP inhibits renal cell carcinoma progression by regulating inflammation and apoptosis
Kang Yang1, Yusha Xiao2, Tao Xu1
1Department of Urology, Renmin Hospital of Wuhan University, Wuhan, Hubei, China.
Abstract:
Patients with renal cell carcinoma (RCC) usually develop drug resistance and have poor prognosis owing to its insensitive property. However, the underlying mechanisms of RCC are still unclear. We implemented an integrative analysis of The Cancer Genome Atlas and Gene Expression Omnibus datasets. Three genes (CRHBP, RAB25 and PSAT1) were found to be potential biomarkers in ccRCC and validated by four independent cohorts. Then, ccRCC patients with a decreased expression of CRHBP in tumor tissues had significantly poor survival by TCGA ccRCC datasets and verified by clinical samples as well as RCC cell lines. Overexpression of CRHBP suppressed cell proliferation, migration, invasion as well as apoptosis in vitro and in vivo. Moreover, the results of western blot analysis showed the effects of CRHBP via upregulating NF-κB and p53-mediated mitochondria apoptotic pathway. Our results suggested that CRHBP may be an effective target to treat ccRCC patients.
Insights
Discovering novel biomarkers for kidney cancer is crucial. This study identifies CRHBP as a potential therapeutic target for clear cell renal cell carcinoma (ccRCC), showing its role in suppressing tumor growth and improving patient survival.
Area of Science:
- Oncology
- Molecular Biology
- Genomics
Background:
- Renal cell carcinoma (RCC) often exhibits drug resistance and poor prognosis.
- The underlying molecular mechanisms driving RCC progression remain incompletely understood.
Purpose of the Study:
- To identify potential biomarkers and therapeutic targets for clear cell renal cell carcinoma (ccRCC).
- To elucidate the functional role of identified biomarkers in ccRCC development and progression.
Main Methods:
- Integrative analysis of The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) datasets.
- Validation of candidate biomarkers across four independent cohorts, clinical samples, and RCC cell lines.
- In vitro and in vivo experiments to assess the functional impact of biomarker overexpression.
- Western blot analysis to investigate the molecular pathways involved.
Main Results:
- Three genes (CRHBP, RAB25, PSAT1) were identified as potential ccRCC biomarkers.
- Decreased CRHBP expression in ccRCC tumors correlated with significantly poorer patient survival.
- Overexpression of CRHBP suppressed tumor cell proliferation, migration, invasion, and apoptosis.
- CRHBP functions by upregulating the NF-κB and p53-mediated mitochondrial apoptotic pathway.
Conclusions:
- CRHBP is a potential prognostic biomarker for ccRCC.
- CRHBP acts as a tumor suppressor in ccRCC.
- CRHBP represents a promising therapeutic target for ccRCC treatment.
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