The genomic landscape of metastatic clear cell renal cell carcinoma after systemic therapy. Academic Article uri icon

Overview

abstract

  • Primary clear cell renal cell carcinoma (ccRCC) has been previously characterized, but the genomic landscape of metastatic ccRCC is largely unexplored. Here, we performed whole exome sequencing (WES) in 68 samples from 44 patients with ccRCC, including 52 samples from a metastatic site. SETD2, PBRM1, APC and VHL were the most frequently mutated genes in the metastatic ccRCC cohort. RBM10 and FBXW7 were also among the 10 most frequently mutated genes in metastatic tissues. Recurrent somatic copy number variations (CNV) were observed at the previously identified regions 3p25, 9p21 and 14q25, but also at 6p21 (CDKN1A) and 13q14 (RB1). No statistically significant differences were found between samples from therapy-naïve and pretreated patients. Clonal evolution analyses with multiple samples from 13 patients suggested that early appearance of CNVs at 3p25, 9p21 and 14q25 may be associated with rapid clinical progression. Overall, the genomic landscapes of primary and metastatic ccRCC seem to share frequent CNVs at 3p25, 9p21 and 14q25. Future work will clarify the implication of RBM10 and FBXW7 mutations and 6p21 and 13q14 CNVs in metastatic ccRCC.

publication date

  • April 5, 2022

Research

keywords

  • Carcinoma, Renal Cell
  • Kidney Neoplasms

Identity

PubMed Central ID

  • PMC9208073

Scopus Document Identifier

  • 85127506270

Digital Object Identifier (DOI)

  • 10.1002/1878-0261.13204

PubMed ID

  • 35231161

Additional Document Info

volume

  • 16

issue

  • 12