Distribution of β‐human chorionic gonadotropin‐positive cells in noncancerous gastric mucosa and in malignant gastric tumors
The authors examined the localization and behavior of β‐human chorionic gonadotropin (HCG)‐positive cells in human gastric noncancerous mucosa and in gastric malignant tumors, using immunohistochemistry and the anti‐β‐HCG antibody. The β‐HCG‐positive cells were located mainly in the antral mucosa an...
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Veröffentlicht in: | Cancer 1990-08, Vol.66 (4), p.695-701 |
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description | The authors examined the localization and behavior of β‐human chorionic gonadotropin (HCG)‐positive cells in human gastric noncancerous mucosa and in gastric malignant tumors, using immunohistochemistry and the anti‐β‐HCG antibody. The β‐HCG‐positive cells were located mainly in the antral mucosa and were generally restricted to the neck portion of the pyloric glands, although a few were present in fundic glands of the gastric body. The β‐HCG‐immunoreactive cells were found in gastric carcinomas in 53% of the 92 cases examined. These cells were observed more often in advanced carcinomas that were histologically poorly differentiated than in early carcinomas or in well‐differentiated tumors, but this prevalence had no statistical significance. The presence of the β‐HCG‐positive cells in the gastric carcinomas suggested no appreciable prognostic significance, even quantitatively. In the syncytiotrophoblast‐like tumor cells seen in four gastric tumor samples with histologic features of a choriocarcinoma, immunoreactivity to the β‐HCG was striking. There was, however, no recognizable dominance in the number of β‐HCG‐reactive cells in the noncancerous mucosa around the tumor. |
doi_str_mv | 10.1002/1097-0142(19900815)66:4<695::AID-CNCR2820660418>3.0.CO;2-N |
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The β‐HCG‐positive cells were located mainly in the antral mucosa and were generally restricted to the neck portion of the pyloric glands, although a few were present in fundic glands of the gastric body. The β‐HCG‐immunoreactive cells were found in gastric carcinomas in 53% of the 92 cases examined. These cells were observed more often in advanced carcinomas that were histologically poorly differentiated than in early carcinomas or in well‐differentiated tumors, but this prevalence had no statistical significance. The presence of the β‐HCG‐positive cells in the gastric carcinomas suggested no appreciable prognostic significance, even quantitatively. In the syncytiotrophoblast‐like tumor cells seen in four gastric tumor samples with histologic features of a choriocarcinoma, immunoreactivity to the β‐HCG was striking. There was, however, no recognizable dominance in the number of β‐HCG‐reactive cells in the noncancerous mucosa around the tumor.</description><identifier>ISSN: 0008-543X</identifier><identifier>EISSN: 1097-0142</identifier><identifier>DOI: 10.1002/1097-0142(19900815)66:4<695::AID-CNCR2820660418>3.0.CO;2-N</identifier><identifier>PMID: 1696845</identifier><identifier>CODEN: CANCAR</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adenocarcinoma - analysis ; Biological and medical sciences ; Choriocarcinoma - analysis ; Chorionic Gonadotropin - analysis ; Chorionic Gonadotropin, beta Subunit, Human ; Cytoplasm - analysis ; Female ; Gastric Fundus - analysis ; Gastric Mucosa - analysis ; Gastric Mucosa - cytology ; Gastroenterology. Liver. Pancreas. Abdomen ; Humans ; Immunohistochemistry ; Male ; Medical sciences ; Peptide Fragments - analysis ; Pyloric Antrum - analysis ; Reference Values ; Stomach Neoplasms - analysis ; Stomach Neoplasms - pathology ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Tumors</subject><ispartof>Cancer, 1990-08, Vol.66 (4), p.695-701</ispartof><rights>Copyright © 1990 American Cancer Society</rights><rights>1991 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4968-c45fcdcbc39c44cf218568948add4c72f6ec6ded8d2bd394d913847f21b37f9f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19624134$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1696845$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yakeishi, Yoichi</creatorcontrib><creatorcontrib>Mori, Masaki</creatorcontrib><creatorcontrib>Enjoji, Munetomo</creatorcontrib><title>Distribution of β‐human chorionic gonadotropin‐positive cells in noncancerous gastric mucosa and in malignant gastric tumors</title><title>Cancer</title><addtitle>Cancer</addtitle><description>The authors examined the localization and behavior of β‐human chorionic gonadotropin (HCG)‐positive cells in human gastric noncancerous mucosa and in gastric malignant tumors, using immunohistochemistry and the anti‐β‐HCG antibody. The β‐HCG‐positive cells were located mainly in the antral mucosa and were generally restricted to the neck portion of the pyloric glands, although a few were present in fundic glands of the gastric body. The β‐HCG‐immunoreactive cells were found in gastric carcinomas in 53% of the 92 cases examined. These cells were observed more often in advanced carcinomas that were histologically poorly differentiated than in early carcinomas or in well‐differentiated tumors, but this prevalence had no statistical significance. The presence of the β‐HCG‐positive cells in the gastric carcinomas suggested no appreciable prognostic significance, even quantitatively. In the syncytiotrophoblast‐like tumor cells seen in four gastric tumor samples with histologic features of a choriocarcinoma, immunoreactivity to the β‐HCG was striking. There was, however, no recognizable dominance in the number of β‐HCG‐reactive cells in the noncancerous mucosa around the tumor.</description><subject>Adenocarcinoma - analysis</subject><subject>Biological and medical sciences</subject><subject>Choriocarcinoma - analysis</subject><subject>Chorionic Gonadotropin - analysis</subject><subject>Chorionic Gonadotropin, beta Subunit, Human</subject><subject>Cytoplasm - analysis</subject><subject>Female</subject><subject>Gastric Fundus - analysis</subject><subject>Gastric Mucosa - analysis</subject><subject>Gastric Mucosa - cytology</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Peptide Fragments - analysis</subject><subject>Pyloric Antrum - analysis</subject><subject>Reference Values</subject><subject>Stomach Neoplasms - analysis</subject><subject>Stomach Neoplasms - pathology</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>Tumors</subject><issn>0008-543X</issn><issn>1097-0142</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkU2KFDEcxYMoY8_oEYRsFF1Um69KVVoRxho_BoZuEAVxE9JJqidSlbRJ1cjs9AaexYN4CE9iim5n0IXgJiF5vzxe_g-A5xjNMULkMUaiKhBm5CEWAqEal484X7CnXJSLxfHpSdEsmzekJohzxHD9jM7RvFk9IcXyBphdPb4JZig_LkpG398Ghyl9zMeKlPQAHGAueM3KGfh64tIQ3XocXPAwtPDH959fvp2PvfJQn4eYb52Gm-CVCUMMW-ezvA3JDe7CQm27LkHnoQ9eK69tDGOCGzVZatiPOiQFlTcT0qvObbzyw5U-jH2I6Q641aou2bv7_Qi8e_nibfO6OFu9Om2OzwrNcta8lq02eq2p0IzpluC65LVgtTKG6Yq03GpurKkNWRsqmBGY1qzK3JpWrWjpEXiw893G8Gm0aZC9S9MHlLc5tayEYKzENIMfdqCOIaVoW7mNrlfxUmIkp37kNGI5jVj-7kdyLpnM_UiZ-5F_9iOpRLJZSSKX2fzePsW47q25tt4VkvX7e10lrbo25qm6dI0JThimLHN2x312nb38r4T_DPiXQn8BDFvA-Q</recordid><startdate>19900815</startdate><enddate>19900815</enddate><creator>Yakeishi, Yoichi</creator><creator>Mori, Masaki</creator><creator>Enjoji, Munetomo</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>IQODW</scope><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>7X8</scope></search><sort><creationdate>19900815</creationdate><title>Distribution of β‐human chorionic gonadotropin‐positive cells in noncancerous gastric mucosa and in malignant gastric tumors</title><author>Yakeishi, Yoichi ; Mori, Masaki ; Enjoji, Munetomo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4968-c45fcdcbc39c44cf218568948add4c72f6ec6ded8d2bd394d913847f21b37f9f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>Adenocarcinoma - analysis</topic><topic>Biological and medical sciences</topic><topic>Choriocarcinoma - analysis</topic><topic>Chorionic Gonadotropin - analysis</topic><topic>Chorionic Gonadotropin, beta Subunit, Human</topic><topic>Cytoplasm - analysis</topic><topic>Female</topic><topic>Gastric Fundus - analysis</topic><topic>Gastric Mucosa - analysis</topic><topic>Gastric Mucosa - cytology</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Peptide Fragments - analysis</topic><topic>Pyloric Antrum - analysis</topic><topic>Reference Values</topic><topic>Stomach Neoplasms - analysis</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>Yakeishi, Yoichi</creatorcontrib><creatorcontrib>Mori, Masaki</creatorcontrib><creatorcontrib>Enjoji, Munetomo</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>MEDLINE - Academic</collection><jtitle>Cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yakeishi, Yoichi</au><au>Mori, Masaki</au><au>Enjoji, Munetomo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Distribution of β‐human chorionic gonadotropin‐positive cells in noncancerous gastric mucosa and in malignant gastric tumors</atitle><jtitle>Cancer</jtitle><addtitle>Cancer</addtitle><date>1990-08-15</date><risdate>1990</risdate><volume>66</volume><issue>4</issue><spage>695</spage><epage>701</epage><pages>695-701</pages><issn>0008-543X</issn><eissn>1097-0142</eissn><coden>CANCAR</coden><abstract>The authors examined the localization and behavior of β‐human chorionic gonadotropin (HCG)‐positive cells in human gastric noncancerous mucosa and in gastric malignant tumors, using immunohistochemistry and the anti‐β‐HCG antibody. The β‐HCG‐positive cells were located mainly in the antral mucosa and were generally restricted to the neck portion of the pyloric glands, although a few were present in fundic glands of the gastric body. The β‐HCG‐immunoreactive cells were found in gastric carcinomas in 53% of the 92 cases examined. These cells were observed more often in advanced carcinomas that were histologically poorly differentiated than in early carcinomas or in well‐differentiated tumors, but this prevalence had no statistical significance. The presence of the β‐HCG‐positive cells in the gastric carcinomas suggested no appreciable prognostic significance, even quantitatively. In the syncytiotrophoblast‐like tumor cells seen in four gastric tumor samples with histologic features of a choriocarcinoma, immunoreactivity to the β‐HCG was striking. There was, however, no recognizable dominance in the number of β‐HCG‐reactive cells in the noncancerous mucosa around the tumor.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>1696845</pmid><doi>10.1002/1097-0142(19900815)66:4<695::AID-CNCR2820660418>3.0.CO;2-N</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenocarcinoma - analysis Biological and medical sciences Choriocarcinoma - analysis Chorionic Gonadotropin - analysis Chorionic Gonadotropin, beta Subunit, Human Cytoplasm - analysis Female Gastric Fundus - analysis Gastric Mucosa - analysis Gastric Mucosa - cytology Gastroenterology. Liver. Pancreas. Abdomen Humans Immunohistochemistry Male Medical sciences Peptide Fragments - analysis Pyloric Antrum - analysis Reference Values Stomach Neoplasms - analysis Stomach Neoplasms - pathology Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Tumors |
title | Distribution of β‐human chorionic gonadotropin‐positive cells in noncancerous gastric mucosa and in malignant gastric tumors |
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