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Article

Chromosome 17p13 deletion is associated with an aggressive tumor phenotype in clear cell renal cell carcinoma.

World journal of surgical oncology - 13 Jun 2020

Eichenauer Till, Shadanpour Navid, Kluth Martina, Göbel Cosima, Weidemann Sören, Fraune Christoph, Büscheck Franziska, Hube-Magg Claudia, Möller-Koop Christina, Dahlem Roland, Fisch Margit, Rink Michael, Riechardt Silke, Burandt Eike, Bernreuther Christian, Minner Sarah, Simon Ronald, Sauter Guido, Wilczak Waldemar, Clauditz Till

Abstract excerpt

BACKGROUND: Deletions of 17p13 recurrently occur in renal cell carcinoma (RCC) but their prognostic role seems to be uncertain. METHODS: To determine prevalence, relationship with tumor phenotype, and patient prognosis, a tissue microarray containing samples from 1809 RCCs was evaluated using dual labeling fluorescence in situ hybridization (FISH) with 17p13 and chromosome 17 centromere probes. RESULTS: A 17p13...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 17

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Identifiers

PMID: 32534597
DOI: 10.1186/s12957-020-01902-y
PMCID: PMC7293794

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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