DYSF expression in clear cell renal cell carcinoma: A retrospective study of 2 independent cohorts
•Higher expression of DYSF is associated with better prognosis of ccRCC patients.•DYSF expression in tumor tissue is higher than that in normal tissue.•DYSF gene might be a potential prognostic biomarker for ccRCC patients. Renal cell carcinoma (RCC) is the most typical type of kidney cancer in adul...
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Veröffentlicht in: | Urologic oncology 2019-10, Vol.37 (10), p.735-741 |
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Zusammenfassung: | •Higher expression of DYSF is associated with better prognosis of ccRCC patients.•DYSF expression in tumor tissue is higher than that in normal tissue.•DYSF gene might be a potential prognostic biomarker for ccRCC patients.
Renal cell carcinoma (RCC) is the most typical type of kidney cancer in adults. Hypercalcemia is a well known paraneoplastic syndrome associated with RCC and recent studies have reported that hypercalcemia is closely related to the poor prognosis of RCC patients. Clear cell RCC (ccRCC) is the most common and aggressive subtype of RCC. Although the histological classification of RCC is important for determination of appropriate treatment strategies, effective biomarkers for predicting prognosis of ccRCC have not yet been identified. Since calcium levels affect the prognosis of RCC patients, we evaluated whether the calcium-sensing genes on the plasma membrane, including those encoding calcium channels, CaSR, GPRC6a, and DYSF, could be used as biomarkers to predict the prognosis of ccRCC patients.
Information from 537 patients from The Cancer Genome Atlas (TCGA; n = 446) and International Cancer Genome Consortium (ICGC; n = 91) was used in this study. Among these genes, DYSF was the only gene whose expression correlated with overall survival of both TGCA and ICGC patients.
Although DYSF gene expression was higher in ccRCC tissue than in normal kidney tissue, Kaplan-Meier curves showed that the survival rate of ccRCC patients with high DYSF expression was significantly higher than that of patients with low DYSF expression (TCGA, P |
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ISSN: | 1078-1439 1873-2496 |
DOI: | 10.1016/j.urolonc.2019.07.007 |