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Minichromosome maintenance 2 (MCM2) immunoreactivity in stage III human gastric carcinoma: clinicopathological significance

Background The origin licensing factor minichromosome maintenance 2 (MCM2) has recently been identified as a critical regulator of proliferation in both normal and neoplastic cells. This study examined whether MCM2 expression was of prognostic relevance in patients with stage III gastric carcinoma a...

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Published in:Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association 2008-03, Vol.11 (1), p.37-46
Main Authors: Tokuyasu, Naruo, Shomori, Kohei, Nishihara, Keisuke, Kawaguchi, Hiroki, Fujioka, Shinji, Yamaga, Kensaku, Ikeguchi, Masahide, Ito, Hisao
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container_title Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association
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creator Tokuyasu, Naruo
Shomori, Kohei
Nishihara, Keisuke
Kawaguchi, Hiroki
Fujioka, Shinji
Yamaga, Kensaku
Ikeguchi, Masahide
Ito, Hisao
description Background The origin licensing factor minichromosome maintenance 2 (MCM2) has recently been identified as a critical regulator of proliferation in both normal and neoplastic cells. This study examined whether MCM2 expression was of prognostic relevance in patients with stage III gastric carcinoma and whether the expression of this marker showed any correlation with clinicopathological characteristics. In addition, we evaluated whether the expression of this proliferation marker was correlated with that of another marker, Ki-67, in gastric carcinoma. Methods We examined the immunohistochemical expression of MCM2, Ki-67, and p53 in 103 surgically removed stage III gastric carcinomas, which consisted of 60 intestinal-type and 43 diffuse-type carcinomas. The labeling indices (LIs) of MCM2 and Ki-67 in cancer cells were compared with clinicopathological characteristics, p53 expression, and overall survival rates. Results The mean MCM2 and Ki-67 LIs were 69.1 ± 11.8% and 48.2 ± 14.5%, respectively, in the intestinal carcinomas, and 43.7 ± 9.9% and 24.9 ± 11.0%, respectively, in the diffuse carcinomas. The LIs of these proteins revealed no significant association with clinicopathological characteristics or with p53 expression in the carcinomas. Kaplan-Meier survival curves showed that, in the patients with diffuse carcinoma, those with higher MCM2 LIs had a poorer prognosis ( P < 0.05), but the MCM2 LI was not correlated with prognosis for those with intestinal carcinoma ( P = 0.25). Ki-67 expression had no significant correlation with prognosis in either intestinal-type or diffuse-type carcinomas. Multivariate Cox regression analysis confirmed that MCM2 was an independent prognostic factor in patients with diffuse carcinoma. Conclusion Our data suggest that MCM2 is a useful prognostic marker in patients stage III diffuse-type gastric carcinoma.
doi_str_mv 10.1007/s10120-008-0451-1
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This study examined whether MCM2 expression was of prognostic relevance in patients with stage III gastric carcinoma and whether the expression of this marker showed any correlation with clinicopathological characteristics. In addition, we evaluated whether the expression of this proliferation marker was correlated with that of another marker, Ki-67, in gastric carcinoma. Methods We examined the immunohistochemical expression of MCM2, Ki-67, and p53 in 103 surgically removed stage III gastric carcinomas, which consisted of 60 intestinal-type and 43 diffuse-type carcinomas. The labeling indices (LIs) of MCM2 and Ki-67 in cancer cells were compared with clinicopathological characteristics, p53 expression, and overall survival rates. Results The mean MCM2 and Ki-67 LIs were 69.1 ± 11.8% and 48.2 ± 14.5%, respectively, in the intestinal carcinomas, and 43.7 ± 9.9% and 24.9 ± 11.0%, respectively, in the diffuse carcinomas. The LIs of these proteins revealed no significant association with clinicopathological characteristics or with p53 expression in the carcinomas. Kaplan-Meier survival curves showed that, in the patients with diffuse carcinoma, those with higher MCM2 LIs had a poorer prognosis ( P &lt; 0.05), but the MCM2 LI was not correlated with prognosis for those with intestinal carcinoma ( P = 0.25). Ki-67 expression had no significant correlation with prognosis in either intestinal-type or diffuse-type carcinomas. Multivariate Cox regression analysis confirmed that MCM2 was an independent prognostic factor in patients with diffuse carcinoma. Conclusion Our data suggest that MCM2 is a useful prognostic marker in patients stage III diffuse-type gastric carcinoma.</description><identifier>ISSN: 1436-3291</identifier><identifier>EISSN: 1436-3305</identifier><identifier>DOI: 10.1007/s10120-008-0451-1</identifier><identifier>PMID: 18373176</identifier><language>eng</language><publisher>Japan: Springer Japan</publisher><subject>Abdominal Surgery ; Aged ; Biomarkers, Tumor - analysis ; Biomarkers, Tumor - immunology ; Cancer Research ; Cell Cycle Proteins - analysis ; Cell Cycle Proteins - immunology ; Female ; Fluorescent Antibody Technique ; Gastric cancer ; Gastric Mucosa - chemistry ; Gastric Mucosa - pathology ; Gastroenterology ; Humans ; Immunohistochemistry ; Ki-67 Antigen - analysis ; Male ; Medicine ; Medicine &amp; Public Health ; Minichromosome Maintenance Complex Component 2 ; Models, Statistical ; Neoplasm Staging ; Nuclear Proteins - analysis ; Nuclear Proteins - immunology ; Oncology ; Original Article ; Prognosis ; Stomach Neoplasms - chemistry ; Stomach Neoplasms - mortality ; Stomach Neoplasms - pathology ; Surgical Oncology ; Tumor Suppressor Protein p53 - analysis</subject><ispartof>Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association, 2008-03, Vol.11 (1), p.37-46</ispartof><rights>The International Gastric Cancer Association and The Japanese Gastric Cancer Association 2008</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c467t-39c09de02f84d8a22d8af57cf493573281e34a355753fd3a3ea6c5b8c7ef4ca83</citedby><cites>FETCH-LOGICAL-c467t-39c09de02f84d8a22d8af57cf493573281e34a355753fd3a3ea6c5b8c7ef4ca83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27915,27916</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18373176$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tokuyasu, Naruo</creatorcontrib><creatorcontrib>Shomori, Kohei</creatorcontrib><creatorcontrib>Nishihara, Keisuke</creatorcontrib><creatorcontrib>Kawaguchi, Hiroki</creatorcontrib><creatorcontrib>Fujioka, Shinji</creatorcontrib><creatorcontrib>Yamaga, Kensaku</creatorcontrib><creatorcontrib>Ikeguchi, Masahide</creatorcontrib><creatorcontrib>Ito, Hisao</creatorcontrib><title>Minichromosome maintenance 2 (MCM2) immunoreactivity in stage III human gastric carcinoma: clinicopathological significance</title><title>Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association</title><addtitle>Gastric Cancer</addtitle><addtitle>Gastric Cancer</addtitle><description>Background The origin licensing factor minichromosome maintenance 2 (MCM2) has recently been identified as a critical regulator of proliferation in both normal and neoplastic cells. This study examined whether MCM2 expression was of prognostic relevance in patients with stage III gastric carcinoma and whether the expression of this marker showed any correlation with clinicopathological characteristics. In addition, we evaluated whether the expression of this proliferation marker was correlated with that of another marker, Ki-67, in gastric carcinoma. Methods We examined the immunohistochemical expression of MCM2, Ki-67, and p53 in 103 surgically removed stage III gastric carcinomas, which consisted of 60 intestinal-type and 43 diffuse-type carcinomas. The labeling indices (LIs) of MCM2 and Ki-67 in cancer cells were compared with clinicopathological characteristics, p53 expression, and overall survival rates. Results The mean MCM2 and Ki-67 LIs were 69.1 ± 11.8% and 48.2 ± 14.5%, respectively, in the intestinal carcinomas, and 43.7 ± 9.9% and 24.9 ± 11.0%, respectively, in the diffuse carcinomas. The LIs of these proteins revealed no significant association with clinicopathological characteristics or with p53 expression in the carcinomas. Kaplan-Meier survival curves showed that, in the patients with diffuse carcinoma, those with higher MCM2 LIs had a poorer prognosis ( P &lt; 0.05), but the MCM2 LI was not correlated with prognosis for those with intestinal carcinoma ( P = 0.25). Ki-67 expression had no significant correlation with prognosis in either intestinal-type or diffuse-type carcinomas. Multivariate Cox regression analysis confirmed that MCM2 was an independent prognostic factor in patients with diffuse carcinoma. 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This study examined whether MCM2 expression was of prognostic relevance in patients with stage III gastric carcinoma and whether the expression of this marker showed any correlation with clinicopathological characteristics. In addition, we evaluated whether the expression of this proliferation marker was correlated with that of another marker, Ki-67, in gastric carcinoma. Methods We examined the immunohistochemical expression of MCM2, Ki-67, and p53 in 103 surgically removed stage III gastric carcinomas, which consisted of 60 intestinal-type and 43 diffuse-type carcinomas. The labeling indices (LIs) of MCM2 and Ki-67 in cancer cells were compared with clinicopathological characteristics, p53 expression, and overall survival rates. Results The mean MCM2 and Ki-67 LIs were 69.1 ± 11.8% and 48.2 ± 14.5%, respectively, in the intestinal carcinomas, and 43.7 ± 9.9% and 24.9 ± 11.0%, respectively, in the diffuse carcinomas. The LIs of these proteins revealed no significant association with clinicopathological characteristics or with p53 expression in the carcinomas. Kaplan-Meier survival curves showed that, in the patients with diffuse carcinoma, those with higher MCM2 LIs had a poorer prognosis ( P &lt; 0.05), but the MCM2 LI was not correlated with prognosis for those with intestinal carcinoma ( P = 0.25). Ki-67 expression had no significant correlation with prognosis in either intestinal-type or diffuse-type carcinomas. Multivariate Cox regression analysis confirmed that MCM2 was an independent prognostic factor in patients with diffuse carcinoma. Conclusion Our data suggest that MCM2 is a useful prognostic marker in patients stage III diffuse-type gastric carcinoma.</abstract><cop>Japan</cop><pub>Springer Japan</pub><pmid>18373176</pmid><doi>10.1007/s10120-008-0451-1</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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subjects Abdominal Surgery
Aged
Biomarkers, Tumor - analysis
Biomarkers, Tumor - immunology
Cancer Research
Cell Cycle Proteins - analysis
Cell Cycle Proteins - immunology
Female
Fluorescent Antibody Technique
Gastric cancer
Gastric Mucosa - chemistry
Gastric Mucosa - pathology
Gastroenterology
Humans
Immunohistochemistry
Ki-67 Antigen - analysis
Male
Medicine
Medicine & Public Health
Minichromosome Maintenance Complex Component 2
Models, Statistical
Neoplasm Staging
Nuclear Proteins - analysis
Nuclear Proteins - immunology
Oncology
Original Article
Prognosis
Stomach Neoplasms - chemistry
Stomach Neoplasms - mortality
Stomach Neoplasms - pathology
Surgical Oncology
Tumor Suppressor Protein p53 - analysis
title Minichromosome maintenance 2 (MCM2) immunoreactivity in stage III human gastric carcinoma: clinicopathological significance
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