Hybrid oncocytic/chromophobe renal tumors are molecularly distinct from oncocytoma and chromophobe renal cell carcinoma View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2019-06-23

AUTHORS

Roberto Ruiz-Cordero, Priya Rao, Lerong Li, Yuan Qi, Daniel Atherton, Bo Peng, Rajesh R. Singh, Tae-Beom Kim, Fumi Kawakami, Mark J. Routbort, Nail Alouch, Chi-Wan B. Chow, Ximing Tang, Wei Lu, Fadi Brimo, Surena F. Matin, Christopher G. Wood, Nizar M. Tannir, Ignacio I. Wistuba, Ken Chen, Jing Wang, L. Jeffrey Medeiros, Jose A. Karam, Pheroze Tamboli, Kanishka Sircar

ABSTRACT

Hybrid oncocytic/chromophobe tumor (HOCT) of the kidney represents a poorly understood clinicopathologic entity with pathologic features that overlap between benign renal oncocytoma (RO) and malignant chromophobe renal cell carcinoma (ChRCC). Consequently, characterization of HOCT and its separation from the foregoing entities are clinically important. The aim of this study was to describe the pathologic and molecular features of HOCT and to compare them with those of RO and ChRCC. We retrospectively identified a cohort of 73 cases with renal oncocytic tumors (19 RO, 27 HOCT, and 27 ChRCC) for whom clinical follow-up data were available by 2 tertiary care hospitals. All cases were sporadic except for 2 HOCTs that were associated with Birt–Hogg–Dubé syndrome. Lesional tissues were retrieved for molecular analysis. We performed targeted gene sequencing of all exons of 261 cancer related genes on a subset of HOCT samples (n = 16). Gene expression profiling of a customized codeset was conducted on 19 RO, 24 HOCT, and 27 ChRCC samples. Clinicopathologic characteristics as well as DNA copy number alterations, mutational and transcriptional features of HOCT derived from sequencing and expression profiling data are described and compared to those in RO and ChRCC. HOCTs were more frequently multifocal and did not exhibit mutations in genes that are recurrently mutated in RO or ChRCC but showed copy number alterations primarily involving losses in chromosomes 1 and X/Y. The mRNA transcript data show that HOCT can be separated from RO and ChRCC. Hence, HOCT appears to represent a distinct renal tumor entity with genomic features that are intermediate between those of RO and ChRCC. More... »

PAGES

1698-1707

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/s41379-019-0304-y

DOI

http://dx.doi.org/10.1038/s41379-019-0304-y

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1117471349

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/31231128


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