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Pepsinogens I and II in Gastric Cancer: An Immunohistochemical Study Using Monoclonal Antibodies
Monoclonal antibodies were used to examine the immunohistochemical expression of pepsinogens I and II in 31 early and 76 advanced gastric cancers. Of the 107 carcinomas studied, 19 contained pepsinogen II and only 3, found exclusively in pepsinogen II‐positive cases, contained pepsinogen I. Gastric...
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Published in: | Cancer science 1988-10, Vol.79 (10), p.1139-1146 |
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container_title | Cancer science |
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creator | Huang, Shih Che Miki, Kazumasa Sano, Junjiro Ichinose, Masao Kawamura, Norio Oka, Hiroshi Hirano, Kazuyuki Furihata, Chie Masugi, Yozo Takahashi, Kenji |
description | Monoclonal antibodies were used to examine the immunohistochemical expression of pepsinogens I and II in 31 early and 76 advanced gastric cancers. Of the 107 carcinomas studied, 19 contained pepsinogen II and only 3, found exclusively in pepsinogen II‐positive cases, contained pepsinogen I. Gastric cancer produces pepsinogen II more frequently than pepsinogen I, and production of the latter is significantly associated with the former. Historically, there were 54 intestinal‐type and 53 diffuse‐type cancers. The former produced pepsinogen II more frequently than the latter. In the diffuse type, the four pepsinogen II‐positive cases were found exclusively in females. Although the pepsinogen expression was independent of the macroscopic features in advanced gastric cancer, it was found that the protruded‐type early gastric cancer produced pepsinogen II more frequently than the depressed type. Incidences of pepsinogen positivity were not different between early and advanced gastric cancers or between cancers with or without lymph node metastasis, suggesting that production of pepsinogen is independent of tumor growth. |
doi_str_mv | 10.1111/j.1349-7006.1988.tb01537.x |
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Of the 107 carcinomas studied, 19 contained pepsinogen II and only 3, found exclusively in pepsinogen II‐positive cases, contained pepsinogen I. Gastric cancer produces pepsinogen II more frequently than pepsinogen I, and production of the latter is significantly associated with the former. Historically, there were 54 intestinal‐type and 53 diffuse‐type cancers. The former produced pepsinogen II more frequently than the latter. In the diffuse type, the four pepsinogen II‐positive cases were found exclusively in females. Although the pepsinogen expression was independent of the macroscopic features in advanced gastric cancer, it was found that the protruded‐type early gastric cancer produced pepsinogen II more frequently than the depressed type. Incidences of pepsinogen positivity were not different between early and advanced gastric cancers or between cancers with or without lymph node metastasis, suggesting that production of pepsinogen is independent of tumor growth.</description><identifier>ISSN: 0910-5050</identifier><identifier>ISSN: 1347-9032</identifier><identifier>EISSN: 1349-7006</identifier><identifier>EISSN: 1876-4673</identifier><identifier>DOI: 10.1111/j.1349-7006.1988.tb01537.x</identifier><identifier>PMID: 3143702</identifier><identifier>CODEN: GANNA2</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Aged ; Antibodies, Monoclonal ; Biological and medical sciences ; Carcinoma ; Female ; Gastric cancer ; Gastric Mucosa - enzymology ; Gastroenterology. Liver. Pancreas. Abdomen ; Humans ; Immunohistochemistry ; Intestine ; Lymph nodes ; Lymphatic Metastasis ; Male ; Medical sciences ; Metastases ; Middle Aged ; Monoclonal antibodies ; Monoclonal antibody ; Pepsinogen ; Pepsinogens - analysis ; Stomach Neoplasms - enzymology ; Stomach Neoplasms - pathology ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Tumors</subject><ispartof>Cancer science, 1988-10, Vol.79 (10), p.1139-1146</ispartof><rights>1989 INIST-CNRS</rights><rights>Copyright John Wiley & Sons, Inc. Oct 1988</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5159-1f05e5f3cf649c2804b49d30f30f6e86314f23fa8438a1e579e7600d9ef460753</citedby><cites>FETCH-LOGICAL-c5159-1f05e5f3cf649c2804b49d30f30f6e86314f23fa8438a1e579e7600d9ef460753</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2400166193/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2400166193?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,44566,53766,53768,74869</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7062071$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3143702$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Huang, Shih Che</creatorcontrib><creatorcontrib>Miki, Kazumasa</creatorcontrib><creatorcontrib>Sano, Junjiro</creatorcontrib><creatorcontrib>Ichinose, Masao</creatorcontrib><creatorcontrib>Kawamura, Norio</creatorcontrib><creatorcontrib>Oka, Hiroshi</creatorcontrib><creatorcontrib>Hirano, Kazuyuki</creatorcontrib><creatorcontrib>Furihata, Chie</creatorcontrib><creatorcontrib>Masugi, Yozo</creatorcontrib><creatorcontrib>Takahashi, Kenji</creatorcontrib><title>Pepsinogens I and II in Gastric Cancer: An Immunohistochemical Study Using Monoclonal Antibodies</title><title>Cancer science</title><addtitle>Jpn J Cancer Res</addtitle><description>Monoclonal antibodies were used to examine the immunohistochemical expression of pepsinogens I and II in 31 early and 76 advanced gastric cancers. Of the 107 carcinomas studied, 19 contained pepsinogen II and only 3, found exclusively in pepsinogen II‐positive cases, contained pepsinogen I. Gastric cancer produces pepsinogen II more frequently than pepsinogen I, and production of the latter is significantly associated with the former. Historically, there were 54 intestinal‐type and 53 diffuse‐type cancers. The former produced pepsinogen II more frequently than the latter. In the diffuse type, the four pepsinogen II‐positive cases were found exclusively in females. Although the pepsinogen expression was independent of the macroscopic features in advanced gastric cancer, it was found that the protruded‐type early gastric cancer produced pepsinogen II more frequently than the depressed type. Incidences of pepsinogen positivity were not different between early and advanced gastric cancers or between cancers with or without lymph node metastasis, suggesting that production of pepsinogen is independent of tumor growth.</description><subject>Aged</subject><subject>Antibodies, Monoclonal</subject><subject>Biological and medical sciences</subject><subject>Carcinoma</subject><subject>Female</subject><subject>Gastric cancer</subject><subject>Gastric Mucosa - enzymology</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Intestine</subject><subject>Lymph nodes</subject><subject>Lymphatic Metastasis</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Metastases</subject><subject>Middle Aged</subject><subject>Monoclonal antibodies</subject><subject>Monoclonal antibody</subject><subject>Pepsinogen</subject><subject>Pepsinogens - analysis</subject><subject>Stomach Neoplasms - enzymology</subject><subject>Stomach Neoplasms - pathology</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. 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Liver. Pancreas. Abdomen</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Intestine</topic><topic>Lymph nodes</topic><topic>Lymphatic Metastasis</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Metastases</topic><topic>Middle Aged</topic><topic>Monoclonal antibodies</topic><topic>Monoclonal antibody</topic><topic>Pepsinogen</topic><topic>Pepsinogens - analysis</topic><topic>Stomach Neoplasms - enzymology</topic><topic>Stomach Neoplasms - pathology</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Huang, Shih Che</creatorcontrib><creatorcontrib>Miki, Kazumasa</creatorcontrib><creatorcontrib>Sano, Junjiro</creatorcontrib><creatorcontrib>Ichinose, Masao</creatorcontrib><creatorcontrib>Kawamura, Norio</creatorcontrib><creatorcontrib>Oka, Hiroshi</creatorcontrib><creatorcontrib>Hirano, Kazuyuki</creatorcontrib><creatorcontrib>Furihata, Chie</creatorcontrib><creatorcontrib>Masugi, Yozo</creatorcontrib><creatorcontrib>Takahashi, Kenji</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>Biological Sciences</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancer science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Huang, Shih Che</au><au>Miki, Kazumasa</au><au>Sano, Junjiro</au><au>Ichinose, Masao</au><au>Kawamura, Norio</au><au>Oka, Hiroshi</au><au>Hirano, Kazuyuki</au><au>Furihata, Chie</au><au>Masugi, Yozo</au><au>Takahashi, Kenji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pepsinogens I and II in Gastric Cancer: An Immunohistochemical Study Using Monoclonal Antibodies</atitle><jtitle>Cancer science</jtitle><addtitle>Jpn J Cancer Res</addtitle><date>1988-10</date><risdate>1988</risdate><volume>79</volume><issue>10</issue><spage>1139</spage><epage>1146</epage><pages>1139-1146</pages><issn>0910-5050</issn><issn>1347-9032</issn><eissn>1349-7006</eissn><eissn>1876-4673</eissn><coden>GANNA2</coden><abstract>Monoclonal antibodies were used to examine the immunohistochemical expression of pepsinogens I and II in 31 early and 76 advanced gastric cancers. Of the 107 carcinomas studied, 19 contained pepsinogen II and only 3, found exclusively in pepsinogen II‐positive cases, contained pepsinogen I. Gastric cancer produces pepsinogen II more frequently than pepsinogen I, and production of the latter is significantly associated with the former. Historically, there were 54 intestinal‐type and 53 diffuse‐type cancers. The former produced pepsinogen II more frequently than the latter. In the diffuse type, the four pepsinogen II‐positive cases were found exclusively in females. Although the pepsinogen expression was independent of the macroscopic features in advanced gastric cancer, it was found that the protruded‐type early gastric cancer produced pepsinogen II more frequently than the depressed type. Incidences of pepsinogen positivity were not different between early and advanced gastric cancers or between cancers with or without lymph node metastasis, suggesting that production of pepsinogen is independent of tumor growth.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>3143702</pmid><doi>10.1111/j.1349-7006.1988.tb01537.x</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Antibodies, Monoclonal Biological and medical sciences Carcinoma Female Gastric cancer Gastric Mucosa - enzymology Gastroenterology. Liver. Pancreas. Abdomen Humans Immunohistochemistry Intestine Lymph nodes Lymphatic Metastasis Male Medical sciences Metastases Middle Aged Monoclonal antibodies Monoclonal antibody Pepsinogen Pepsinogens - analysis Stomach Neoplasms - enzymology Stomach Neoplasms - pathology Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Tumors |
title | Pepsinogens I and II in Gastric Cancer: An Immunohistochemical Study Using Monoclonal Antibodies |
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