4.4 Article

Overexpression of chemokine receptor lymphotactin receptor 1 has prognostic value in clear cell renal cell carcinoma

Journal

MOLECULAR GENETICS & GENOMIC MEDICINE
Volume 9, Issue 1, Pages -

Publisher

WILEY
DOI: 10.1002/mgg3.1551

Keywords

ccRCC; prognosis; STAT; TCGA; XCR1

Funding

  1. National Natural Science Foundation of China [81602591, 81672653, 81972519]

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The study showed that higher XCR1 expression in ccRCC is associated with longer overall survival, and XCR1 knockdown significantly promotes proliferation and migration while reducing apoptosis of renal cell carcinoma cells. XCR1 may serve as a prognostic biomarker for ccRCC in the future.
Background: Clear cell renal cell carcinoma (ccRCC) is an aggressive subtype of renal cell carcinoma. X-C motif chemokine receptor 1 (XCR1) exerts important roles in tumor progression; however, its role in ccRCC is unclear. Methods: We utilized publicly available data from The Cancer Genome Atlas (TCGA) to assess the role of XCR1 in ccRCC and validated the results in 36 samples from patients with ccRCC who underwent curative resection in Xinqiao Hospital Chongqing. XCR1 overexpression was identified in ccRCC, which was confirmed by qRT-PCR assay and immunohistochemical staining of ccRCC samples. Results: For the TCGA and clinical data, Kaplan-Meier survival analysis revealed that higher XCR1 expression in ccRCC was related to longer overall survival. Cox regression analysis suggested that XCR1 is an independent risk factor for ccRCC. GSEA analysis suggested that XCR1 is associated with the JAK/STAT signaling pathway. XCR1 knockdown by small interfering RNA (siRNA) significantly increased ccRCC cell proliferation and migration, and decreased cell apoptosis. Conclusion: We found higher XCR1 expression in ccRCC compared with that in normal tissues is related to longer overall survival in patients with ccRCC. XCR1 knockdown significantly increased RCC cells proliferation and migration, and decreased apoptosis. XCR1 might be used as a prognostic biomarker in ccRCC in the future.

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