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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 |
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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 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_70440195</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>70440195</sourcerecordid><originalsourceid>FETCH-LOGICAL-c467t-39c09de02f84d8a22d8af57cf493573281e34a355753fd3a3ea6c5b8c7ef4ca83</originalsourceid><addsrcrecordid>eNqFkU2LFDEQhoO4uOvqD_AiwcOih9ZUPjrd3mTwY2AHL3oOtZl0T5ZOMibdwuKf3wwzsiDIXqoK8tRbhIeQV8DeA2P6QwEGnDWMdQ2TChp4Qi5AirYRgqmnf2fewzl5XsotY6B6aJ-Rc-iEFqDbC_Jn46O3u5xCKik4GtDH2UWM1lFO325WG_6O-hCWmLJDO_vffr6jPtIy4-joer2muyVgpCOWOXtLLWbrYwr4kdrpkJ32OO_SlEZvcaLFj9EPdawHXpCzAafiXp76Jfn55fOP1bfm-vvX9erTdWNlq-dG9Jb1W8f40Mlth5zXMihtB9kLpQXvwAmJQimtxLAVKBy2Vt10VrtBWuzEJbk65u5z-rW4Mpvgi3XThNGlpRjNpGTQq0fBA6M06Aq--Qe8TUuO9ROGC8647vq-QnCEbE6lZDeYffYB850BZg7-zNGfqf7MwZ-BuvP6FLzcBLd92DgJqwA_AqU-xdHlh8v_T70H0L6mJA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>232027899</pqid></control><display><type>article</type><title>Minichromosome maintenance 2 (MCM2) immunoreactivity in stage III human gastric carcinoma: clinicopathological significance</title><source>Springer Nature</source><creator>Tokuyasu, Naruo ; Shomori, Kohei ; Nishihara, Keisuke ; Kawaguchi, Hiroki ; Fujioka, Shinji ; Yamaga, Kensaku ; Ikeguchi, Masahide ; Ito, Hisao</creator><creatorcontrib>Tokuyasu, Naruo ; Shomori, Kohei ; Nishihara, Keisuke ; Kawaguchi, Hiroki ; Fujioka, Shinji ; Yamaga, Kensaku ; Ikeguchi, Masahide ; Ito, Hisao</creatorcontrib><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.</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 & 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
< 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><subject>Abdominal Surgery</subject><subject>Aged</subject><subject>Biomarkers, Tumor - analysis</subject><subject>Biomarkers, Tumor - immunology</subject><subject>Cancer Research</subject><subject>Cell Cycle Proteins - analysis</subject><subject>Cell Cycle Proteins - immunology</subject><subject>Female</subject><subject>Fluorescent Antibody Technique</subject><subject>Gastric cancer</subject><subject>Gastric Mucosa - chemistry</subject><subject>Gastric Mucosa - pathology</subject><subject>Gastroenterology</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Ki-67 Antigen - analysis</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Minichromosome Maintenance Complex Component 2</subject><subject>Models, Statistical</subject><subject>Neoplasm Staging</subject><subject>Nuclear Proteins - analysis</subject><subject>Nuclear Proteins - immunology</subject><subject>Oncology</subject><subject>Original Article</subject><subject>Prognosis</subject><subject>Stomach Neoplasms - chemistry</subject><subject>Stomach Neoplasms - mortality</subject><subject>Stomach Neoplasms - pathology</subject><subject>Surgical Oncology</subject><subject>Tumor Suppressor Protein p53 - analysis</subject><issn>1436-3291</issn><issn>1436-3305</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqFkU2LFDEQhoO4uOvqD_AiwcOih9ZUPjrd3mTwY2AHL3oOtZl0T5ZOMibdwuKf3wwzsiDIXqoK8tRbhIeQV8DeA2P6QwEGnDWMdQ2TChp4Qi5AirYRgqmnf2fewzl5XsotY6B6aJ-Rc-iEFqDbC_Jn46O3u5xCKik4GtDH2UWM1lFO325WG_6O-hCWmLJDO_vffr6jPtIy4-joer2muyVgpCOWOXtLLWbrYwr4kdrpkJ32OO_SlEZvcaLFj9EPdawHXpCzAafiXp76Jfn55fOP1bfm-vvX9erTdWNlq-dG9Jb1W8f40Mlth5zXMihtB9kLpQXvwAmJQimtxLAVKBy2Vt10VrtBWuzEJbk65u5z-rW4Mpvgi3XThNGlpRjNpGTQq0fBA6M06Aq--Qe8TUuO9ROGC8647vq-QnCEbE6lZDeYffYB850BZg7-zNGfqf7MwZ-BuvP6FLzcBLd92DgJqwA_AqU-xdHlh8v_T70H0L6mJA</recordid><startdate>20080301</startdate><enddate>20080301</enddate><creator>Tokuyasu, Naruo</creator><creator>Shomori, Kohei</creator><creator>Nishihara, Keisuke</creator><creator>Kawaguchi, Hiroki</creator><creator>Fujioka, Shinji</creator><creator>Yamaga, Kensaku</creator><creator>Ikeguchi, Masahide</creator><creator>Ito, Hisao</creator><general>Springer Japan</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20080301</creationdate><title>Minichromosome maintenance 2 (MCM2) immunoreactivity in stage III human gastric carcinoma: clinicopathological significance</title><author>Tokuyasu, Naruo ; 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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.</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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