Publication: Clinical significance and EZH2, ERG and SPINK1 protein expression in pure and mixed ductal adenocarcinoma of the prostate
Authors
Patil, Pallavi A. ; McKenney, Jesse K. ; Reynolds, Jordan P. ; Przybycin, Christopher G. ; Magi Galluzzi, Cristina
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Publisher
Universidad de Murcia. Departamento de BiologĂa Celular e HistologĂa
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DOI
DOI: 10.14670/HH-18-046
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info:eu-repo/semantics/article
Description
Abstract
Background: Although ERG and SPINK1
molecular alterations have been studied in acinar and
ductal adenocarcinoma of the prostate, EZH2 expression
has not been previously evaluated in ductal
adenocarcinoma. Methods: We collected cases of pure
and mixed ductal adenocarcinoma of the prostate and
evaluated clinical significance and EZH2, ERG, and
SPINK1 protein expression. Results: We investigated 61
ductal adenocarcinomas, 22 pure and 39 mixed
ductal/acinar. Except for tumor growth pattern, none of
the clinical parameters studied significantly differed
between pure and mixed tumors. Thirty-five percent of
ductal adenocarcinomas were organ confined, 15%
displayed seminal vesicle invasion. Lymph node and
distal metastasis occurred in 13% and 24% of cases,
respectively; 34% of patients experienced biochemical
failure, 7% died of disease. Ninety-eight percent of
tumors expressed EZH2; in 80% of cases >50% of tumor
cells were positive. ERG and SPINK1 were expressed in
20% and 36% of cases, respectively. There was no
difference in protein expression between pure and mixed
ductal adenocarcinomas. ERG expression tended to be
lower, and SPINK1 higher than reported for acinar
tumors. Biochemical failure, metastasis and death did
not differ between EZH2, ERG, and SPINK1 positive
and negative patients, nor between <50% versus >50%
expression of SPINK1 and EZH2, respectively.
Conclusions: Pure and mixed ductal adenocarcinomas
have similar clinical behavior and molecular alterations.
Higher EZH2 and SPINK1 protein expression, compared
to acinar prostatic adenocarcinoma, might account for
the more aggressive clinical course of ductal
adenocarcinoma
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Citation
Histology and Histopathology, Vol.34, nÂş4, (2019)
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