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Clear cell renal cell carcinoma molecular variations in non-Hispanic White and Hispanic patients.
Batai, Ken; Chen, Yuliang; Rheinheimer, Brenna A; Arora, Amit; Pandey, Ritu; Heimark, Ronald L; Bracamonte, Erika R; Ellis, Nathan A; Lee, Benjamin R.
Afiliação
  • Batai K; Department of Cancer Prevention and Control, Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA.
  • Chen Y; Department of Epidemiology and Biostatistics, University of Arizona, Tucson, Arizona, USA.
  • Rheinheimer BA; Department of Nutritional Sciences, University of Arizona, Tucson, Arizona, USA.
  • Arora A; Department of Epidemiology and Biostatistics, University of Arizona, Tucson, Arizona, USA.
  • Pandey R; Department of Cellular and Molecular Medicine, University of Arizona, Tucson, Arizona, USA.
  • Heimark RL; Department of Surgery, University of Arizona, Tucson, Arizona, USA.
  • Bracamonte ER; Department of Pathology, University of Arizona, Tucson, Arizona, USA.
  • Ellis NA; Department of Cellular and Molecular Medicine, University of Arizona, Tucson, Arizona, USA.
  • Lee BR; Department of Urology, University of Arizona, Tucson, Arizona, USA.
Cancer Med ; 12(11): 12792-12801, 2023 06.
Article em En | MEDLINE | ID: mdl-37081700
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carcinoma de Células Renais / Neoplasias Renais Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carcinoma de Células Renais / Neoplasias Renais Idioma: En Ano de publicação: 2023 Tipo de documento: Article