Integrin expression on colorectal tumor cells growing as monolayers, as multicellular tumor spheroids, or in nude mice
In this study we compared the expression of integrin alpha chains 2, 3, 4, 5, 6, v and the beta chains 1, 3, 4 in 2 colorectal carcinoma cell lines (HRT‐18 and CX‐2), growing in confluent and subconfluent monolayer cultures, as multicellular tumor spheroids and in nude mice, using the immunofluoresc...
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Veröffentlicht in: | International journal of cancer 1995-06, Vol.61 (6), p.819-825 |
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creator | Hauptmann, Steffen Denkert, Carsten Löhrke, Heinz Tietze, Lothar Ott, Stephan Klosterhalfen, Bernd Mittermayer, Christian |
description | In this study we compared the expression of integrin alpha chains 2, 3, 4, 5, 6, v and the beta chains 1, 3, 4 in 2 colorectal carcinoma cell lines (HRT‐18 and CX‐2), growing in confluent and subconfluent monolayer cultures, as multicellular tumor spheroids and in nude mice, using the immunofluorescence technique (confocal microscopy) and flow cytometry. The fast‐growing cell line HRT‐18 expressed, in confluent and subconfluent monolayer cultures, alpha 2, 3 and beta 1 with a continuous membranous staining pattern, whereas alpha v, alpha 6, and beta 4 were expressed continuously membranous in the intermediate and apical part of the cell layer, and clustered at focal contacts at the base of the cells. In spheroids and tumors of nude mice the focal pattern of alpha v, 6 and beta 4 was changed into a diffuse one. Using flow cytometry, the expression of alpha 3 was found to be reduced in spheroids of HRT‐18. The slowly‐growing cell line CX‐2 expressed, under the same conditions in monolayer culture, alpha 6, beta 1 and beta 4, and very weakly alpha 2, 3, 5 and v. Alpha 3 was expressed in spheroids of CX‐2 only at the outer rim where the cells proliferate. In contrast, alpha 2 and 5 were expressed mainly in the quiescent, non‐proliferating area. Alpha 6 was reduced in spheroids of CX‐2. In the nude mouse tumor of CX‐2, alpha 5 was expressed only focally and very weakly, alpha 2 was no longer detectable, but alpha v appeared to be enhanced in a focal pattern. These data indicate that integrin expression of tumor cells depends upon the culture system and that integrin expression in multicellular tumor spheroids is more similar to the in vivo situation in nude mouse tumors. © 1995 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/ijc.2910610613 |
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The fast‐growing cell line HRT‐18 expressed, in confluent and subconfluent monolayer cultures, alpha 2, 3 and beta 1 with a continuous membranous staining pattern, whereas alpha v, alpha 6, and beta 4 were expressed continuously membranous in the intermediate and apical part of the cell layer, and clustered at focal contacts at the base of the cells. In spheroids and tumors of nude mice the focal pattern of alpha v, 6 and beta 4 was changed into a diffuse one. Using flow cytometry, the expression of alpha 3 was found to be reduced in spheroids of HRT‐18. The slowly‐growing cell line CX‐2 expressed, under the same conditions in monolayer culture, alpha 6, beta 1 and beta 4, and very weakly alpha 2, 3, 5 and v. Alpha 3 was expressed in spheroids of CX‐2 only at the outer rim where the cells proliferate. In contrast, alpha 2 and 5 were expressed mainly in the quiescent, non‐proliferating area. Alpha 6 was reduced in spheroids of CX‐2. In the nude mouse tumor of CX‐2, alpha 5 was expressed only focally and very weakly, alpha 2 was no longer detectable, but alpha v appeared to be enhanced in a focal pattern. These data indicate that integrin expression of tumor cells depends upon the culture system and that integrin expression in multicellular tumor spheroids is more similar to the in vivo situation in nude mouse tumors. © 1995 Wiley‐Liss, Inc.</description><identifier>ISSN: 0020-7136</identifier><identifier>EISSN: 1097-0215</identifier><identifier>DOI: 10.1002/ijc.2910610613</identifier><identifier>PMID: 7790117</identifier><identifier>CODEN: IJCNAW</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Animals ; Biological and medical sciences ; Colorectal Neoplasms - metabolism ; Colorectal Neoplasms - pathology ; Flow Cytometry ; Fluorescent Antibody Technique ; Gastroenterology. Liver. Pancreas. Abdomen ; Humans ; Integrins - biosynthesis ; Medical sciences ; Mice ; Mice, Nude ; Microscopy, Confocal ; Neoplasm Transplantation ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Tumor Cells, Cultured ; Tumors</subject><ispartof>International journal of cancer, 1995-06, Vol.61 (6), p.819-825</ispartof><rights>Copyright © 1995 Wiley‐Liss, Inc., A Wiley Company</rights><rights>1995 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3383-80702763e19820ec29ebaff2760dd5e2da2034834ec398908c00ddb6bfd748d43</citedby><cites>FETCH-LOGICAL-c3383-80702763e19820ec29ebaff2760dd5e2da2034834ec398908c00ddb6bfd748d43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fijc.2910610613$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fijc.2910610613$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3594436$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7790117$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hauptmann, Steffen</creatorcontrib><creatorcontrib>Denkert, Carsten</creatorcontrib><creatorcontrib>Löhrke, Heinz</creatorcontrib><creatorcontrib>Tietze, Lothar</creatorcontrib><creatorcontrib>Ott, Stephan</creatorcontrib><creatorcontrib>Klosterhalfen, Bernd</creatorcontrib><creatorcontrib>Mittermayer, Christian</creatorcontrib><title>Integrin expression on colorectal tumor cells growing as monolayers, as multicellular tumor spheroids, or in nude mice</title><title>International journal of cancer</title><addtitle>Int J Cancer</addtitle><description>In this study we compared the expression of integrin alpha chains 2, 3, 4, 5, 6, v and the beta chains 1, 3, 4 in 2 colorectal carcinoma cell lines (HRT‐18 and CX‐2), growing in confluent and subconfluent monolayer cultures, as multicellular tumor spheroids and in nude mice, using the immunofluorescence technique (confocal microscopy) and flow cytometry. The fast‐growing cell line HRT‐18 expressed, in confluent and subconfluent monolayer cultures, alpha 2, 3 and beta 1 with a continuous membranous staining pattern, whereas alpha v, alpha 6, and beta 4 were expressed continuously membranous in the intermediate and apical part of the cell layer, and clustered at focal contacts at the base of the cells. In spheroids and tumors of nude mice the focal pattern of alpha v, 6 and beta 4 was changed into a diffuse one. Using flow cytometry, the expression of alpha 3 was found to be reduced in spheroids of HRT‐18. The slowly‐growing cell line CX‐2 expressed, under the same conditions in monolayer culture, alpha 6, beta 1 and beta 4, and very weakly alpha 2, 3, 5 and v. Alpha 3 was expressed in spheroids of CX‐2 only at the outer rim where the cells proliferate. In contrast, alpha 2 and 5 were expressed mainly in the quiescent, non‐proliferating area. Alpha 6 was reduced in spheroids of CX‐2. In the nude mouse tumor of CX‐2, alpha 5 was expressed only focally and very weakly, alpha 2 was no longer detectable, but alpha v appeared to be enhanced in a focal pattern. These data indicate that integrin expression of tumor cells depends upon the culture system and that integrin expression in multicellular tumor spheroids is more similar to the in vivo situation in nude mouse tumors. © 1995 Wiley‐Liss, Inc.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Colorectal Neoplasms - metabolism</subject><subject>Colorectal Neoplasms - pathology</subject><subject>Flow Cytometry</subject><subject>Fluorescent Antibody Technique</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Humans</subject><subject>Integrins - biosynthesis</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Nude</subject><subject>Microscopy, Confocal</subject><subject>Neoplasm Transplantation</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>Tumor Cells, Cultured</subject><subject>Tumors</subject><issn>0020-7136</issn><issn>1097-0215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkL1PwzAQxS0EKqWwsiFlYCTlHOfLI6r4KKrEAnPkOJfiyokjOwH63-PSqLAhnWSf3-_dWY-QSwpzChDdqo2cR5xCuit2RKYUeBZCRJNjMvUAhBll6Sk5c24DQGkC8YRMsoz7ezYlH8u2x7VVbYBfnUXnlGkDX9JoY1H2Qgf90BgbSNTaBWtrPlW7DoQLGtMaLbZo3c1PO-he7aBBCzt6XPeO1qjKE77zO9qhwqDx2Dk5qYV2eDGeM_L2cP-6eApXL4_Lxd0qlIzlLMwhgyhLGVKeR4Ay4liKuvZPUFUJRpWIgMU5i1EynnPIJXihTMu6yuK8itmMzPdzpTXOWayLzqpG2G1BodjlV_j8it_8vOFqb-iGssHqgI-Bef161IWTQtdWtFK5A8YSHscs9RjfY59K4_afpcXyefHnC9_op4qr</recordid><startdate>19950609</startdate><enddate>19950609</enddate><creator>Hauptmann, Steffen</creator><creator>Denkert, Carsten</creator><creator>Löhrke, Heinz</creator><creator>Tietze, Lothar</creator><creator>Ott, Stephan</creator><creator>Klosterhalfen, Bernd</creator><creator>Mittermayer, Christian</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></search><sort><creationdate>19950609</creationdate><title>Integrin expression on colorectal tumor cells growing as monolayers, as multicellular tumor spheroids, or in nude mice</title><author>Hauptmann, Steffen ; Denkert, Carsten ; Löhrke, Heinz ; Tietze, Lothar ; Ott, Stephan ; Klosterhalfen, Bernd ; Mittermayer, Christian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3383-80702763e19820ec29ebaff2760dd5e2da2034834ec398908c00ddb6bfd748d43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Colorectal Neoplasms - metabolism</topic><topic>Colorectal Neoplasms - pathology</topic><topic>Flow Cytometry</topic><topic>Fluorescent Antibody Technique</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Humans</topic><topic>Integrins - biosynthesis</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Nude</topic><topic>Microscopy, Confocal</topic><topic>Neoplasm Transplantation</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>Tumor Cells, Cultured</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hauptmann, Steffen</creatorcontrib><creatorcontrib>Denkert, Carsten</creatorcontrib><creatorcontrib>Löhrke, Heinz</creatorcontrib><creatorcontrib>Tietze, Lothar</creatorcontrib><creatorcontrib>Ott, Stephan</creatorcontrib><creatorcontrib>Klosterhalfen, Bernd</creatorcontrib><creatorcontrib>Mittermayer, Christian</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><jtitle>International journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hauptmann, Steffen</au><au>Denkert, Carsten</au><au>Löhrke, Heinz</au><au>Tietze, Lothar</au><au>Ott, Stephan</au><au>Klosterhalfen, Bernd</au><au>Mittermayer, Christian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Integrin expression on colorectal tumor cells growing as monolayers, as multicellular tumor spheroids, or in nude mice</atitle><jtitle>International journal of cancer</jtitle><addtitle>Int J Cancer</addtitle><date>1995-06-09</date><risdate>1995</risdate><volume>61</volume><issue>6</issue><spage>819</spage><epage>825</epage><pages>819-825</pages><issn>0020-7136</issn><eissn>1097-0215</eissn><coden>IJCNAW</coden><abstract>In this study we compared the expression of integrin alpha chains 2, 3, 4, 5, 6, v and the beta chains 1, 3, 4 in 2 colorectal carcinoma cell lines (HRT‐18 and CX‐2), growing in confluent and subconfluent monolayer cultures, as multicellular tumor spheroids and in nude mice, using the immunofluorescence technique (confocal microscopy) and flow cytometry. The fast‐growing cell line HRT‐18 expressed, in confluent and subconfluent monolayer cultures, alpha 2, 3 and beta 1 with a continuous membranous staining pattern, whereas alpha v, alpha 6, and beta 4 were expressed continuously membranous in the intermediate and apical part of the cell layer, and clustered at focal contacts at the base of the cells. In spheroids and tumors of nude mice the focal pattern of alpha v, 6 and beta 4 was changed into a diffuse one. Using flow cytometry, the expression of alpha 3 was found to be reduced in spheroids of HRT‐18. The slowly‐growing cell line CX‐2 expressed, under the same conditions in monolayer culture, alpha 6, beta 1 and beta 4, and very weakly alpha 2, 3, 5 and v. Alpha 3 was expressed in spheroids of CX‐2 only at the outer rim where the cells proliferate. In contrast, alpha 2 and 5 were expressed mainly in the quiescent, non‐proliferating area. Alpha 6 was reduced in spheroids of CX‐2. In the nude mouse tumor of CX‐2, alpha 5 was expressed only focally and very weakly, alpha 2 was no longer detectable, but alpha v appeared to be enhanced in a focal pattern. These data indicate that integrin expression of tumor cells depends upon the culture system and that integrin expression in multicellular tumor spheroids is more similar to the in vivo situation in nude mouse tumors. © 1995 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>7790117</pmid><doi>10.1002/ijc.2910610613</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Colorectal Neoplasms - metabolism Colorectal Neoplasms - pathology Flow Cytometry Fluorescent Antibody Technique Gastroenterology. Liver. Pancreas. Abdomen Humans Integrins - biosynthesis Medical sciences Mice Mice, Nude Microscopy, Confocal Neoplasm Transplantation Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Tumor Cells, Cultured Tumors |
title | Integrin expression on colorectal tumor cells growing as monolayers, as multicellular tumor spheroids, or in nude mice |
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