Clear cell renal cell carcinoma molecular variations in non-Hispanic White and Hispanic patients
Author
Batai, K.Chen, Y.
Rheinheimer, B.A.
Arora, A.
Pandey, R.
Heimark, R.L.
Bracamonte, E.R.
Ellis, N.A.
Lee, B.R.
Affiliation
Department of Epidemiology and Biostatistics, University of ArizonaDepartment of Nutritional Sciences, University of Arizona
Department of Epidemiology and Biostatistics, University of Arizona
Department of Cellular and Molecular Medicine, University of Arizona
Department of Surgery, University of Arizona
Department of Pathology, University of Arizona
Department of Urology, University of Arizona
Issue Date
2023-04-20Keywords
gene expression and diversity Hispanics and European Americans (comparison)health disparities
molecular subtype
VHL
Metadata
Show full item recordPublisher
John Wiley and Sons IncCitation
Batai K, Chen Y, Rheinheimer BA, et al. Clear cell renal cell carcinoma molecular variations in non-Hispanic White and Hispanic patients. Cancer Med. 2023; 12: 12792-12801. doi:10.1002/cam4.5929Journal
Cancer MedicineRights
© 2023 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution License.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Background: The United States is becoming increasingly diverse, but few molecular studies have assessed the progression of clear cell renal cell carcinoma (ccRCC) in diverse patient populations. This study examined ccRCC molecular variations in non-Hispanic White (NHW) and Hispanic patients and their effect on the association of gene expression with high-grade (Grade 3 or 4) ccRCC and overall mortality. Methods: A total of 156 patients were included in VHL sequencing and/or TempO-Seq analysis. DESeq2 was used to identify the genes associated with high-grade ccRCC. Logistic regression analysis was performed to assess whether race and ethnicity was associated with high/moderate impact VHL somatic mutations and the ccA/ccB subtype. Cox regression analysis was performed to assess association of molecular subtype and gene expression with overall mortality. Results: NHWs had moderate or high impact mutations in the VHL gene at a higher frequency than Hispanics (40.2% vs. 27.4%), while Hispanics had a higher frequency of the ccA subtype than NHWs (61.9% vs. 45.8%). ccA was more common in patients with BMI≥35 (65.2%) than in those with BMI < 25 (45.0%). There were 11 differentially expressed genes between high- and low-grade tumors. The Haptoglobin (HP) gene was most significantly overexpressed in high- compared to low-grade ccRCC in all samples (p-adj = 1.7 × 10−12). When stratified by subtype, the 11 genes were significantly differentially expressed in the ccB subtype, but none of them were significant after adjusting for multiple testing in ccA. Finally, patients with the ccB subtype had a significantly increased risk of overall mortality (HR 4.87; p = 0.01) compared to patients with ccA, and patients with high HP expression and ccB, had a significantly increased risk of mortality compared to those with low HP expression and ccA (HR 6.45, p = 0.04). Conclusion: This study reports ccRCC molecular variations in Hispanic patients who were previously underrepresented. © 2023 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.Note
Open access journalISSN
2045-7634PubMed ID
37081700Version
Final Published Versionae974a485f413a2113503eed53cd6c53
10.1002/cam4.5929
Scopus Count
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Except where otherwise noted, this item's license is described as © 2023 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution License.
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