Ovarian mucinous tumors frequently express markers of gastric, intestinal, and pancreatobiliary epithelial cells
In 100 mucinous tumors of the ovary (37 benign, 24 borderline, and 39 malignant), the authors determined by histochemical and immunohistochemical techniques the frequencies and patterns of expression of a total of nine markers of gastric, intestinal, and pancreatobiliary duct epithelial cells. M1, a...
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Veröffentlicht in: | Cancer 1992-04, Vol.69 (8), p.2131-2142 |
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description | In 100 mucinous tumors of the ovary (37 benign, 24 borderline, and 39 malignant), the authors determined by histochemical and immunohistochemical techniques the frequencies and patterns of expression of a total of nine markers of gastric, intestinal, and pancreatobiliary duct epithelial cells. M1, a mucin antigen, and cathepsin E (CaE), an aspartic proteinase, two markers of normal gastric superficial/foveolar epithelial cells, were expressed in 95 and 92 tumors, respectively. Periodic acid‐concanavalin A—reactive much or pepsinogen (PG) II, markers of gastric mucus neck and pyloric gland cells, were found in 79 tumors. All of these tumors also expressed M1 or CaE. DU‐PAN‐2 and the N‐terminal epitope of gastrin‐releasing peptide, markers of normal pancreatobiliary duct cells, were found in 70 and 49 tumors, respectively, and CAR‐5 and M3SI, markers of intestinal mucin, were expressed in 51 and 30 tumors, respectively. All tumors expressed at least two of the nine markers studied; none expressed PG I, a marker of gastric chief cells. The mucopeptic cell marker, PG II, was significantly more common in benign and borderline than in malignant tumors (P < 0.005), whereas CAR‐5 and M3SI, markers of intestinal mucin, were expressed significantly more often in malignant than in benign and borderline tumors (P < 0.001). By electron microscopic examination, many tumor cells had fine structural features characteristic of gastric superficial/foveolar and pyloric gland cells, intestinal columnar or goblet cells, and endocervical cells. The results indicate that gastroenteropancreatic cell differentiation—and, in particular, gastric type differentiation—is a prominent feature of ovarian mucinous tumors. |
doi_str_mv | 10.1002/1097-0142(19920415)69:8<2131::AID-CNCR2820690820>3.0.CO;2-A |
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Michael ; Solcia, Enrico</creator><creatorcontrib>Tenti, Patrizia ; Aguzzi, Alessandra ; Riva, Cristina ; Usellini, Luciana ; Zappatore, Rita ; Bara, Jacques ; Samloff, I. Michael ; Solcia, Enrico</creatorcontrib><description>In 100 mucinous tumors of the ovary (37 benign, 24 borderline, and 39 malignant), the authors determined by histochemical and immunohistochemical techniques the frequencies and patterns of expression of a total of nine markers of gastric, intestinal, and pancreatobiliary duct epithelial cells. M1, a mucin antigen, and cathepsin E (CaE), an aspartic proteinase, two markers of normal gastric superficial/foveolar epithelial cells, were expressed in 95 and 92 tumors, respectively. Periodic acid‐concanavalin A—reactive much or pepsinogen (PG) II, markers of gastric mucus neck and pyloric gland cells, were found in 79 tumors. All of these tumors also expressed M1 or CaE. DU‐PAN‐2 and the N‐terminal epitope of gastrin‐releasing peptide, markers of normal pancreatobiliary duct cells, were found in 70 and 49 tumors, respectively, and CAR‐5 and M3SI, markers of intestinal mucin, were expressed in 51 and 30 tumors, respectively. All tumors expressed at least two of the nine markers studied; none expressed PG I, a marker of gastric chief cells. The mucopeptic cell marker, PG II, was significantly more common in benign and borderline than in malignant tumors (P < 0.005), whereas CAR‐5 and M3SI, markers of intestinal mucin, were expressed significantly more often in malignant than in benign and borderline tumors (P < 0.001). By electron microscopic examination, many tumor cells had fine structural features characteristic of gastric superficial/foveolar and pyloric gland cells, intestinal columnar or goblet cells, and endocervical cells. The results indicate that gastroenteropancreatic cell differentiation—and, in particular, gastric type differentiation—is a prominent feature of ovarian mucinous tumors.</description><identifier>ISSN: 0008-543X</identifier><identifier>EISSN: 1097-0142</identifier><identifier>DOI: 10.1002/1097-0142(19920415)69:8<2131::AID-CNCR2820690820>3.0.CO;2-A</identifier><identifier>PMID: 1311984</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adenocarcinoma, Mucinous - immunology ; Adenocarcinoma, Mucinous - pathology ; Adenocarcinoma, Mucinous - ultrastructure ; Antigens, Differentiation - analysis ; Bile Ducts - cytology ; Digestive System - cytology ; Epithelium - immunology ; Female ; Gastric Mucosa - cytology ; Humans ; Immunoenzyme Techniques ; Intestinal Mucosa - cytology ; Ovarian Neoplasms - immunology ; Ovarian Neoplasms - pathology ; Ovarian Neoplasms - ultrastructure ; Pancreas - cytology</subject><ispartof>Cancer, 1992-04, Vol.69 (8), p.2131-2142</ispartof><rights>Copyright © 1992 American Cancer Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3840-625c4917bd2f53320635142ba50645c13e0494c5d078f18211ef3736db9f04ae3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1311984$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tenti, Patrizia</creatorcontrib><creatorcontrib>Aguzzi, Alessandra</creatorcontrib><creatorcontrib>Riva, Cristina</creatorcontrib><creatorcontrib>Usellini, Luciana</creatorcontrib><creatorcontrib>Zappatore, Rita</creatorcontrib><creatorcontrib>Bara, Jacques</creatorcontrib><creatorcontrib>Samloff, I. Michael</creatorcontrib><creatorcontrib>Solcia, Enrico</creatorcontrib><title>Ovarian mucinous tumors frequently express markers of gastric, intestinal, and pancreatobiliary epithelial cells</title><title>Cancer</title><addtitle>Cancer</addtitle><description>In 100 mucinous tumors of the ovary (37 benign, 24 borderline, and 39 malignant), the authors determined by histochemical and immunohistochemical techniques the frequencies and patterns of expression of a total of nine markers of gastric, intestinal, and pancreatobiliary duct epithelial cells. M1, a mucin antigen, and cathepsin E (CaE), an aspartic proteinase, two markers of normal gastric superficial/foveolar epithelial cells, were expressed in 95 and 92 tumors, respectively. Periodic acid‐concanavalin A—reactive much or pepsinogen (PG) II, markers of gastric mucus neck and pyloric gland cells, were found in 79 tumors. All of these tumors also expressed M1 or CaE. DU‐PAN‐2 and the N‐terminal epitope of gastrin‐releasing peptide, markers of normal pancreatobiliary duct cells, were found in 70 and 49 tumors, respectively, and CAR‐5 and M3SI, markers of intestinal mucin, were expressed in 51 and 30 tumors, respectively. All tumors expressed at least two of the nine markers studied; none expressed PG I, a marker of gastric chief cells. The mucopeptic cell marker, PG II, was significantly more common in benign and borderline than in malignant tumors (P < 0.005), whereas CAR‐5 and M3SI, markers of intestinal mucin, were expressed significantly more often in malignant than in benign and borderline tumors (P < 0.001). By electron microscopic examination, many tumor cells had fine structural features characteristic of gastric superficial/foveolar and pyloric gland cells, intestinal columnar or goblet cells, and endocervical cells. The results indicate that gastroenteropancreatic cell differentiation—and, in particular, gastric type differentiation—is a prominent feature of ovarian mucinous tumors.</description><subject>Adenocarcinoma, Mucinous - immunology</subject><subject>Adenocarcinoma, Mucinous - pathology</subject><subject>Adenocarcinoma, Mucinous - ultrastructure</subject><subject>Antigens, Differentiation - analysis</subject><subject>Bile Ducts - cytology</subject><subject>Digestive System - cytology</subject><subject>Epithelium - immunology</subject><subject>Female</subject><subject>Gastric Mucosa - cytology</subject><subject>Humans</subject><subject>Immunoenzyme Techniques</subject><subject>Intestinal Mucosa - cytology</subject><subject>Ovarian Neoplasms - immunology</subject><subject>Ovarian Neoplasms - pathology</subject><subject>Ovarian Neoplasms - ultrastructure</subject><subject>Pancreas - cytology</subject><issn>0008-543X</issn><issn>1097-0142</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVUV2L1TAQDaKs19WfIORJFLbXyUfb5CrCpe4XLF4QBcGHIW1TjfbLpF33_ntT7qrog-DLZMKZOTNnDiEFgzUD4M8Z6DwBJvlTpjUHydJnmd6ol5wJttlsL18nxZviLVccMg0xvhJrWBe7FzzZ3iGrX913yQoAVJJK8eE-eRDCl_jNeSqOyFFkYlrJFRl318Y709Nurlw_zIFOczf4QBtvv822n9o9tTejtyHQzvivNkJDQz-ZMHlXnVDXTzZMrjftCTV9TUfTV96aaShd64yPzaObPtuYt7SybRseknuNaYN9dPsek_dnp--Ki-Rqd35ZbK-SSigJScbTSmqWlzVvUiGiVJFGTaVJIZNpxYQFqWWV1pCrhinOmG1ELrK61A1IY8UxeXLgHf0QhYQJOxeWDUxvo0zMuZIsVyoWfjwUVn4IwdsGR--i1D0ywMUPXC6Ky0Xxpx-YaVS4-IEY_cA__UCBgMUOOW4j--PbNeays_Vv7oMBEW8O-HfX2v3_jf7n5L8Q8QP6x6lV</recordid><startdate>19920415</startdate><enddate>19920415</enddate><creator>Tenti, Patrizia</creator><creator>Aguzzi, Alessandra</creator><creator>Riva, Cristina</creator><creator>Usellini, Luciana</creator><creator>Zappatore, Rita</creator><creator>Bara, Jacques</creator><creator>Samloff, I. Michael</creator><creator>Solcia, Enrico</creator><general>Wiley Subscription Services, Inc., A Wiley Company</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>7X8</scope></search><sort><creationdate>19920415</creationdate><title>Ovarian mucinous tumors frequently express markers of gastric, intestinal, and pancreatobiliary epithelial cells</title><author>Tenti, Patrizia ; Aguzzi, Alessandra ; Riva, Cristina ; Usellini, Luciana ; Zappatore, Rita ; Bara, Jacques ; Samloff, I. Michael ; Solcia, Enrico</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3840-625c4917bd2f53320635142ba50645c13e0494c5d078f18211ef3736db9f04ae3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Adenocarcinoma, Mucinous - immunology</topic><topic>Adenocarcinoma, Mucinous - pathology</topic><topic>Adenocarcinoma, Mucinous - ultrastructure</topic><topic>Antigens, Differentiation - analysis</topic><topic>Bile Ducts - cytology</topic><topic>Digestive System - cytology</topic><topic>Epithelium - immunology</topic><topic>Female</topic><topic>Gastric Mucosa - cytology</topic><topic>Humans</topic><topic>Immunoenzyme Techniques</topic><topic>Intestinal Mucosa - cytology</topic><topic>Ovarian Neoplasms - immunology</topic><topic>Ovarian Neoplasms - pathology</topic><topic>Ovarian Neoplasms - ultrastructure</topic><topic>Pancreas - cytology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tenti, Patrizia</creatorcontrib><creatorcontrib>Aguzzi, Alessandra</creatorcontrib><creatorcontrib>Riva, Cristina</creatorcontrib><creatorcontrib>Usellini, Luciana</creatorcontrib><creatorcontrib>Zappatore, Rita</creatorcontrib><creatorcontrib>Bara, Jacques</creatorcontrib><creatorcontrib>Samloff, I. Michael</creatorcontrib><creatorcontrib>Solcia, Enrico</creatorcontrib><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>Tenti, Patrizia</au><au>Aguzzi, Alessandra</au><au>Riva, Cristina</au><au>Usellini, Luciana</au><au>Zappatore, Rita</au><au>Bara, Jacques</au><au>Samloff, I. Michael</au><au>Solcia, Enrico</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ovarian mucinous tumors frequently express markers of gastric, intestinal, and pancreatobiliary epithelial cells</atitle><jtitle>Cancer</jtitle><addtitle>Cancer</addtitle><date>1992-04-15</date><risdate>1992</risdate><volume>69</volume><issue>8</issue><spage>2131</spage><epage>2142</epage><pages>2131-2142</pages><issn>0008-543X</issn><eissn>1097-0142</eissn><abstract>In 100 mucinous tumors of the ovary (37 benign, 24 borderline, and 39 malignant), the authors determined by histochemical and immunohistochemical techniques the frequencies and patterns of expression of a total of nine markers of gastric, intestinal, and pancreatobiliary duct epithelial cells. M1, a mucin antigen, and cathepsin E (CaE), an aspartic proteinase, two markers of normal gastric superficial/foveolar epithelial cells, were expressed in 95 and 92 tumors, respectively. Periodic acid‐concanavalin A—reactive much or pepsinogen (PG) II, markers of gastric mucus neck and pyloric gland cells, were found in 79 tumors. All of these tumors also expressed M1 or CaE. DU‐PAN‐2 and the N‐terminal epitope of gastrin‐releasing peptide, markers of normal pancreatobiliary duct cells, were found in 70 and 49 tumors, respectively, and CAR‐5 and M3SI, markers of intestinal mucin, were expressed in 51 and 30 tumors, respectively. All tumors expressed at least two of the nine markers studied; none expressed PG I, a marker of gastric chief cells. The mucopeptic cell marker, PG II, was significantly more common in benign and borderline than in malignant tumors (P < 0.005), whereas CAR‐5 and M3SI, markers of intestinal mucin, were expressed significantly more often in malignant than in benign and borderline tumors (P < 0.001). By electron microscopic examination, many tumor cells had fine structural features characteristic of gastric superficial/foveolar and pyloric gland cells, intestinal columnar or goblet cells, and endocervical cells. The results indicate that gastroenteropancreatic cell differentiation—and, in particular, gastric type differentiation—is a prominent feature of ovarian mucinous tumors.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>1311984</pmid><doi>10.1002/1097-0142(19920415)69:8<2131::AID-CNCR2820690820>3.0.CO;2-A</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenocarcinoma, Mucinous - immunology Adenocarcinoma, Mucinous - pathology Adenocarcinoma, Mucinous - ultrastructure Antigens, Differentiation - analysis Bile Ducts - cytology Digestive System - cytology Epithelium - immunology Female Gastric Mucosa - cytology Humans Immunoenzyme Techniques Intestinal Mucosa - cytology Ovarian Neoplasms - immunology Ovarian Neoplasms - pathology Ovarian Neoplasms - ultrastructure Pancreas - cytology |
title | Ovarian mucinous tumors frequently express markers of gastric, intestinal, and pancreatobiliary epithelial cells |
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