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

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

Abstract 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...

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Bibliographic Details
Main Authors: Till Eichenauer, Navid Shadanpour, Martina Kluth, Cosima Göbel, Sören Weidemann, Christoph Fraune, Franziska Büscheck, Claudia Hube-Magg, Christina Möller-Koop, Roland Dahlem, Margit Fisch, Michael Rink, Silke Riechardt, Eike Burandt, Christian Bernreuther, Sarah Minner, Ronald Simon, Guido Sauter, Waldemar Wilczak, Till Clauditz
Format: Article
Language:English
Published: BMC 2020-06-01
Series:World Journal of Surgical Oncology
Subjects:
Renal cell cancer
17p13 deletion
Fluorescence in situ hybridization
Tissue microarray
Prognosis
Online Access:http://link.springer.com/article/10.1186/s12957-020-01902-y

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http://link.springer.com/article/10.1186/s12957-020-01902-y

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