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Clinical significance of mismatch repair gene expression in sporadic colorectal cancer

Mismatch repair (MMR) genes play an important role in the occurrence and development of sporadic colorectal cancer; however, the effect of MMR genes on clinicopathological features and prognosis remains unclear. The aim of the present study was to observe the clinical significance of MMR gene expres...

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Autores principales: SUN, ZHENQIANG, YU, XIANBO, WANG, HAIJIANG, ZHANG, SHUO, ZHAO, ZELIANG, XU, RUIWEI
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4186363/
https://www.ncbi.nlm.nih.gov/pubmed/25289032
http://dx.doi.org/10.3892/etm.2014.1927
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author SUN, ZHENQIANG
YU, XIANBO
WANG, HAIJIANG
ZHANG, SHUO
ZHAO, ZELIANG
XU, RUIWEI
author_facet SUN, ZHENQIANG
YU, XIANBO
WANG, HAIJIANG
ZHANG, SHUO
ZHAO, ZELIANG
XU, RUIWEI
author_sort SUN, ZHENQIANG
collection PubMed
description Mismatch repair (MMR) genes play an important role in the occurrence and development of sporadic colorectal cancer; however, the effect of MMR genes on clinicopathological features and prognosis remains unclear. The aim of the present study was to observe the clinical significance of MMR gene expression in sporadic colorectal cancer. Clinicopathological data and postoperative samples from 404 patients with sporadic colorectal cancer were obtained from the Affiliated Tumor Hospital of Xinjiang Medical University. The immunohistochemistry PV-9000 two-step method was performed to measure the protein expression of human mutL homolog 1 (hMLH1), human mutS homolog (hMSH) 2, human postmeiotic segregation increased 2 (hPSM2) and hMSH6. Differences in clinicopathological features, family history and survival time subsequent to surgery between groups with normal and aberrant MMR protein (MMRP) expression were compared. A total of 27.23% of all patients showed aberrant nuclear staining of MMRP. Among the patients with aberrant MMRP expression, a higher proportion of patients showed aberrant expression of more than one type of MMRP than aberrant expression of only one type of MMRP. Aberrant expression of hMLH1/hPSM2 was most commonly observed (29/404). In addition, aberrant MMRP expression in colorectal cancer was indicated predominantly in the right hemicolon. Histological type primarily showed mucinous adenocarcinoma. In addition, with increasing body mass index (BMI), the MMRP deficiency rate was also shown to increase gradually. There was a close association between MMRP expression deficiency and family history of cancer (P<0.05). For TNM stage III patients, the Kaplan-Meier survival curve showed that the aberrant MMRP expression group had a three-year disease-free survival (DFS) rate of 66.67%, which was longer than the DFS rate of the normal group (55.41%), with no statistical difference (P>0.05). In conclusion, the immunohistochemistry PV-9000 two-step method can be used to measure MMRP expression in colorectal cancer. Aberrant MMRP expression is closely correlated with tumor location, histological type, BMI and tumor family history in sporadic colorectal cancer. Aberrant MMRP expression may have an effect on the prognosis of stage III patients.
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spelling pubmed-41863632014-10-06 Clinical significance of mismatch repair gene expression in sporadic colorectal cancer SUN, ZHENQIANG YU, XIANBO WANG, HAIJIANG ZHANG, SHUO ZHAO, ZELIANG XU, RUIWEI Exp Ther Med Articles Mismatch repair (MMR) genes play an important role in the occurrence and development of sporadic colorectal cancer; however, the effect of MMR genes on clinicopathological features and prognosis remains unclear. The aim of the present study was to observe the clinical significance of MMR gene expression in sporadic colorectal cancer. Clinicopathological data and postoperative samples from 404 patients with sporadic colorectal cancer were obtained from the Affiliated Tumor Hospital of Xinjiang Medical University. The immunohistochemistry PV-9000 two-step method was performed to measure the protein expression of human mutL homolog 1 (hMLH1), human mutS homolog (hMSH) 2, human postmeiotic segregation increased 2 (hPSM2) and hMSH6. Differences in clinicopathological features, family history and survival time subsequent to surgery between groups with normal and aberrant MMR protein (MMRP) expression were compared. A total of 27.23% of all patients showed aberrant nuclear staining of MMRP. Among the patients with aberrant MMRP expression, a higher proportion of patients showed aberrant expression of more than one type of MMRP than aberrant expression of only one type of MMRP. Aberrant expression of hMLH1/hPSM2 was most commonly observed (29/404). In addition, aberrant MMRP expression in colorectal cancer was indicated predominantly in the right hemicolon. Histological type primarily showed mucinous adenocarcinoma. In addition, with increasing body mass index (BMI), the MMRP deficiency rate was also shown to increase gradually. There was a close association between MMRP expression deficiency and family history of cancer (P<0.05). For TNM stage III patients, the Kaplan-Meier survival curve showed that the aberrant MMRP expression group had a three-year disease-free survival (DFS) rate of 66.67%, which was longer than the DFS rate of the normal group (55.41%), with no statistical difference (P>0.05). In conclusion, the immunohistochemistry PV-9000 two-step method can be used to measure MMRP expression in colorectal cancer. Aberrant MMRP expression is closely correlated with tumor location, histological type, BMI and tumor family history in sporadic colorectal cancer. Aberrant MMRP expression may have an effect on the prognosis of stage III patients. D.A. Spandidos 2014-11 2014-08-22 /pmc/articles/PMC4186363/ /pubmed/25289032 http://dx.doi.org/10.3892/etm.2014.1927 Text en Copyright © 2014, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
SUN, ZHENQIANG
YU, XIANBO
WANG, HAIJIANG
ZHANG, SHUO
ZHAO, ZELIANG
XU, RUIWEI
Clinical significance of mismatch repair gene expression in sporadic colorectal cancer
title Clinical significance of mismatch repair gene expression in sporadic colorectal cancer
title_full Clinical significance of mismatch repair gene expression in sporadic colorectal cancer
title_fullStr Clinical significance of mismatch repair gene expression in sporadic colorectal cancer
title_full_unstemmed Clinical significance of mismatch repair gene expression in sporadic colorectal cancer
title_short Clinical significance of mismatch repair gene expression in sporadic colorectal cancer
title_sort clinical significance of mismatch repair gene expression in sporadic colorectal cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4186363/
https://www.ncbi.nlm.nih.gov/pubmed/25289032
http://dx.doi.org/10.3892/etm.2014.1927
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