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Similar protein expression profiles of ovarian and endometrial high-grade serous carcinomas

BACKGROUND: Ovarian and endometrial high-grade serous carcinomas (HGSCs) have similar clinical and pathological characteristics; however, exhaustive protein expression profiling of these cancers has yet to be reported. METHODS: We performed protein expression profiling on 14 cases of HGSCs (7 ovaria...

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Autores principales: Hiramatsu, Kosuke, Yoshino, Kiyoshi, Serada, Satoshi, Yoshihara, Kosuke, Hori, Yumiko, Fujimoto, Minoru, Matsuzaki, Shinya, Egawa-Takata, Tomomi, Kobayashi, Eiji, Ueda, Yutaka, Morii, Eiichi, Enomoto, Takayuki, Naka, Tetsuji, Kimura, Tadashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4782211/
https://www.ncbi.nlm.nih.gov/pubmed/26889980
http://dx.doi.org/10.1038/bjc.2016.27
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author Hiramatsu, Kosuke
Yoshino, Kiyoshi
Serada, Satoshi
Yoshihara, Kosuke
Hori, Yumiko
Fujimoto, Minoru
Matsuzaki, Shinya
Egawa-Takata, Tomomi
Kobayashi, Eiji
Ueda, Yutaka
Morii, Eiichi
Enomoto, Takayuki
Naka, Tetsuji
Kimura, Tadashi
author_facet Hiramatsu, Kosuke
Yoshino, Kiyoshi
Serada, Satoshi
Yoshihara, Kosuke
Hori, Yumiko
Fujimoto, Minoru
Matsuzaki, Shinya
Egawa-Takata, Tomomi
Kobayashi, Eiji
Ueda, Yutaka
Morii, Eiichi
Enomoto, Takayuki
Naka, Tetsuji
Kimura, Tadashi
author_sort Hiramatsu, Kosuke
collection PubMed
description BACKGROUND: Ovarian and endometrial high-grade serous carcinomas (HGSCs) have similar clinical and pathological characteristics; however, exhaustive protein expression profiling of these cancers has yet to be reported. METHODS: We performed protein expression profiling on 14 cases of HGSCs (7 ovarian and 7 endometrial) and 18 endometrioid carcinomas (9 ovarian and 9 endometrial) using iTRAQ-based exhaustive and quantitative protein analysis. RESULTS: We identified 828 tumour-expressed proteins and evaluated the statistical similarity of protein expression profiles between ovarian and endometrial HGSCs using unsupervised hierarchical cluster analysis (P<0.01). Using 45 statistically highly expressed proteins in HGSCs, protein ontology analysis detected two enriched terms and proteins composing each term: IMP2 and MCM2. Immunohistochemical analyses confirmed the higher expression of IMP2 and MCM2 in ovarian and endometrial HGSCs as well as in tubal and peritoneal HGSCs than in endometrioid carcinomas (P<0.01). The knockdown of either IMP2 or MCM2 by siRNA interference significantly decreased the proliferation rate of ovarian HGSC cell line (P<0.01). CONCLUSIONS: We demonstrated the statistical similarity of the protein expression profiles of ovarian and endometrial HGSC beyond the organs. We suggest that increased IMP2 and MCM2 expression may underlie some of the rapid HGSC growth observed clinically.
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spelling pubmed-47822112017-03-01 Similar protein expression profiles of ovarian and endometrial high-grade serous carcinomas Hiramatsu, Kosuke Yoshino, Kiyoshi Serada, Satoshi Yoshihara, Kosuke Hori, Yumiko Fujimoto, Minoru Matsuzaki, Shinya Egawa-Takata, Tomomi Kobayashi, Eiji Ueda, Yutaka Morii, Eiichi Enomoto, Takayuki Naka, Tetsuji Kimura, Tadashi Br J Cancer Molecular Diagnostics BACKGROUND: Ovarian and endometrial high-grade serous carcinomas (HGSCs) have similar clinical and pathological characteristics; however, exhaustive protein expression profiling of these cancers has yet to be reported. METHODS: We performed protein expression profiling on 14 cases of HGSCs (7 ovarian and 7 endometrial) and 18 endometrioid carcinomas (9 ovarian and 9 endometrial) using iTRAQ-based exhaustive and quantitative protein analysis. RESULTS: We identified 828 tumour-expressed proteins and evaluated the statistical similarity of protein expression profiles between ovarian and endometrial HGSCs using unsupervised hierarchical cluster analysis (P<0.01). Using 45 statistically highly expressed proteins in HGSCs, protein ontology analysis detected two enriched terms and proteins composing each term: IMP2 and MCM2. Immunohistochemical analyses confirmed the higher expression of IMP2 and MCM2 in ovarian and endometrial HGSCs as well as in tubal and peritoneal HGSCs than in endometrioid carcinomas (P<0.01). The knockdown of either IMP2 or MCM2 by siRNA interference significantly decreased the proliferation rate of ovarian HGSC cell line (P<0.01). CONCLUSIONS: We demonstrated the statistical similarity of the protein expression profiles of ovarian and endometrial HGSC beyond the organs. We suggest that increased IMP2 and MCM2 expression may underlie some of the rapid HGSC growth observed clinically. Nature Publishing Group 2016-03-01 2016-02-18 /pmc/articles/PMC4782211/ /pubmed/26889980 http://dx.doi.org/10.1038/bjc.2016.27 Text en Copyright © 2016 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Molecular Diagnostics
Hiramatsu, Kosuke
Yoshino, Kiyoshi
Serada, Satoshi
Yoshihara, Kosuke
Hori, Yumiko
Fujimoto, Minoru
Matsuzaki, Shinya
Egawa-Takata, Tomomi
Kobayashi, Eiji
Ueda, Yutaka
Morii, Eiichi
Enomoto, Takayuki
Naka, Tetsuji
Kimura, Tadashi
Similar protein expression profiles of ovarian and endometrial high-grade serous carcinomas
title Similar protein expression profiles of ovarian and endometrial high-grade serous carcinomas
title_full Similar protein expression profiles of ovarian and endometrial high-grade serous carcinomas
title_fullStr Similar protein expression profiles of ovarian and endometrial high-grade serous carcinomas
title_full_unstemmed Similar protein expression profiles of ovarian and endometrial high-grade serous carcinomas
title_short Similar protein expression profiles of ovarian and endometrial high-grade serous carcinomas
title_sort similar protein expression profiles of ovarian and endometrial high-grade serous carcinomas
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4782211/
https://www.ncbi.nlm.nih.gov/pubmed/26889980
http://dx.doi.org/10.1038/bjc.2016.27
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