Colorectal cancer desmoplastic reaction up-regulates collagen synthesis and restricts cancer cell invasion
During cancer cell growth many tumors exhibit various grades of desmoplasia, unorganized production of fibrous or connective tissue, composed mainly of collagen fibers and myofibroblasts. The accumulation of an extracellular matrix (ECM) surrounding tumors directly affects cancer cell proliferation,...
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| Veröffentlicht in: | Cell and tissue research 2011-11, Vol.346 (2), p.223-236 |
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| creator | Coulson-Thomas, Vivien J. Coulson-Thomas, Yvette M. Gesteira, Tarsis F. de Paula, Cláudia A. A. Mader, Ana M. Waisberg, Jaques Pinhal, Maria A. Friedl, Andreas Toma, Leny Nader, Helena B. |
| description | During cancer cell growth many tumors exhibit various grades of desmoplasia, unorganized production of fibrous or connective tissue, composed mainly of collagen fibers and myofibroblasts. The accumulation of an extracellular matrix (ECM) surrounding tumors directly affects cancer cell proliferation, migration and spread; therefore the study of desmoplasia is of vital importance. Stromal fibroblasts surrounding tumors are activated to myofibroblasts and become the primary producers of ECM during desmoplasia. The composition, density and organization of this ECM accumulation play a major role on the influence desmoplasia has upon tumor cells. In this study, we analyzed desmoplasia
in vivo
in human colorectal carcinoma tissue, detecting an up-regulation of collagen I, collagen IV and collagen V in human colorectal cancer desmoplastic reaction. These components were then analyzed
in vitro
co-cultivating colorectal cancer cells (Caco-2 and HCT116) and fibroblasts utilizing various co-culture techniques. Our findings demonstrate that direct cell-cell contact between fibroblasts and colorectal cancer cells evokes an increase in ECM density, composed of unorganized collagens (I, III, IV and V) and proteoglycans (biglycan, fibromodulin, perlecan and versican). The desmoplastic collagen fibers were thick, with an altered orientation, as well as deposited as bundles. This increased ECM density inhibited the migration and invasion of the colorectal tumor cells in both 2D and 3D co-culture systems. Therefore this study sheds light on a possible restricting role desmoplasia could play in colorectal cancer invasion. |
| doi_str_mv | 10.1007/s00441-011-1254-y |
| format | Article |
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in vivo
in human colorectal carcinoma tissue, detecting an up-regulation of collagen I, collagen IV and collagen V in human colorectal cancer desmoplastic reaction. These components were then analyzed
in vitro
co-cultivating colorectal cancer cells (Caco-2 and HCT116) and fibroblasts utilizing various co-culture techniques. Our findings demonstrate that direct cell-cell contact between fibroblasts and colorectal cancer cells evokes an increase in ECM density, composed of unorganized collagens (I, III, IV and V) and proteoglycans (biglycan, fibromodulin, perlecan and versican). The desmoplastic collagen fibers were thick, with an altered orientation, as well as deposited as bundles. This increased ECM density inhibited the migration and invasion of the colorectal tumor cells in both 2D and 3D co-culture systems. Therefore this study sheds light on a possible restricting role desmoplasia could play in colorectal cancer invasion.</description><identifier>ISSN: 0302-766X</identifier><identifier>EISSN: 1432-0878</identifier><identifier>DOI: 10.1007/s00441-011-1254-y</identifier><identifier>PMID: 21987222</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>Aged ; Analysis ; Biomedical and Life Sciences ; Biomedicine ; Cell adhesion & migration ; Cell growth ; Cell Line, Tumor ; Coculture Techniques ; Collagen ; Collagen - biosynthesis ; Collagen - genetics ; Colorectal cancer ; Colorectal Neoplasms - genetics ; Colorectal Neoplasms - metabolism ; Colorectal Neoplasms - pathology ; Extracellular Matrix - genetics ; Extracellular Matrix - metabolism ; Female ; Fibroblasts - metabolism ; Fibroblasts - pathology ; Gastrointestinal diseases ; Gene expression ; Gene Expression Regulation, Neoplastic ; Human Genetics ; Humans ; Male ; Middle Aged ; Molecular Medicine ; Neoplasm Invasiveness ; Protein synthesis ; Proteoglycans - metabolism ; Proteomics ; Regular Article ; Stromal Cells - metabolism ; Stromal Cells - pathology ; Tumors ; Up-Regulation</subject><ispartof>Cell and tissue research, 2011-11, Vol.346 (2), p.223-236</ispartof><rights>Springer-Verlag 2011</rights><rights>COPYRIGHT 2011 Springer</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c468t-476f10f9f371eb97f0bbea4dc62215d9626f4df94d6816dcf0cf99fe2ece53263</citedby><cites>FETCH-LOGICAL-c468t-476f10f9f371eb97f0bbea4dc62215d9626f4df94d6816dcf0cf99fe2ece53263</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00441-011-1254-y$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00441-011-1254-y$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21987222$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Coulson-Thomas, Vivien J.</creatorcontrib><creatorcontrib>Coulson-Thomas, Yvette M.</creatorcontrib><creatorcontrib>Gesteira, Tarsis F.</creatorcontrib><creatorcontrib>de Paula, Cláudia A. A.</creatorcontrib><creatorcontrib>Mader, Ana M.</creatorcontrib><creatorcontrib>Waisberg, Jaques</creatorcontrib><creatorcontrib>Pinhal, Maria A.</creatorcontrib><creatorcontrib>Friedl, Andreas</creatorcontrib><creatorcontrib>Toma, Leny</creatorcontrib><creatorcontrib>Nader, Helena B.</creatorcontrib><title>Colorectal cancer desmoplastic reaction up-regulates collagen synthesis and restricts cancer cell invasion</title><title>Cell and tissue research</title><addtitle>Cell Tissue Res</addtitle><addtitle>Cell Tissue Res</addtitle><description>During cancer cell growth many tumors exhibit various grades of desmoplasia, unorganized production of fibrous or connective tissue, composed mainly of collagen fibers and myofibroblasts. The accumulation of an extracellular matrix (ECM) surrounding tumors directly affects cancer cell proliferation, migration and spread; therefore the study of desmoplasia is of vital importance. Stromal fibroblasts surrounding tumors are activated to myofibroblasts and become the primary producers of ECM during desmoplasia. The composition, density and organization of this ECM accumulation play a major role on the influence desmoplasia has upon tumor cells. In this study, we analyzed desmoplasia
in vivo
in human colorectal carcinoma tissue, detecting an up-regulation of collagen I, collagen IV and collagen V in human colorectal cancer desmoplastic reaction. These components were then analyzed
in vitro
co-cultivating colorectal cancer cells (Caco-2 and HCT116) and fibroblasts utilizing various co-culture techniques. Our findings demonstrate that direct cell-cell contact between fibroblasts and colorectal cancer cells evokes an increase in ECM density, composed of unorganized collagens (I, III, IV and V) and proteoglycans (biglycan, fibromodulin, perlecan and versican). The desmoplastic collagen fibers were thick, with an altered orientation, as well as deposited as bundles. This increased ECM density inhibited the migration and invasion of the colorectal tumor cells in both 2D and 3D co-culture systems. Therefore this study sheds light on a possible restricting role desmoplasia could play in colorectal cancer invasion.</description><subject>Aged</subject><subject>Analysis</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cell adhesion & migration</subject><subject>Cell growth</subject><subject>Cell Line, Tumor</subject><subject>Coculture Techniques</subject><subject>Collagen</subject><subject>Collagen - biosynthesis</subject><subject>Collagen - genetics</subject><subject>Colorectal cancer</subject><subject>Colorectal Neoplasms - genetics</subject><subject>Colorectal Neoplasms - metabolism</subject><subject>Colorectal Neoplasms - pathology</subject><subject>Extracellular Matrix - genetics</subject><subject>Extracellular Matrix - metabolism</subject><subject>Female</subject><subject>Fibroblasts - metabolism</subject><subject>Fibroblasts - pathology</subject><subject>Gastrointestinal diseases</subject><subject>Gene expression</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Human Genetics</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Molecular Medicine</subject><subject>Neoplasm Invasiveness</subject><subject>Protein synthesis</subject><subject>Proteoglycans - metabolism</subject><subject>Proteomics</subject><subject>Regular Article</subject><subject>Stromal Cells - metabolism</subject><subject>Stromal Cells - pathology</subject><subject>Tumors</subject><subject>Up-Regulation</subject><issn>0302-766X</issn><issn>1432-0878</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp1kk-LFDEQxYMo7rj6AbxIo6CnXpN0Ot19XAb_wYIXBW8hk67MZEgnYyotzLc3Te-qK0oOgdTvPaoqj5DnjF4xSru3SKkQrKaM1Yy3oj4_IBsmGl7Tvusfkg1tKK87Kb9dkCeIR0qZkHJ4TC44G_qOc74hx230MYHJ2ldGBwOpGgGnePIaszNVAm2yi6GaT3WC_ex1BqxM9F7vIVR4DvkA6LDSYSww5uRMxjsrA95XLvzQWCyekkdWe4Rnt_cl-fr-3Zftx_rm84dP2-ub2gjZ51p00jJqB9t0DHZDZ-luB1qMRnLO2nGQXFox2kGMsmdyNJYaOwwWOBhoGy6bS_Jm9T2l-H0uLanJ4dKJDhBnVAMVZXkD6wr58i_yGOcUSnMFakQvOBUFerVCe-1BuWBjTtosluq6aVvatrJtCnX1D6qcESZnYgDryvs9wes_BAfQPh8w-nlZNt4H2QqaFBETWHVKbtLprBhVSwzUGgNVYqCWGKhz0by4HWzeTTD-Utz9ewH4CmAphT2k35P_3_Unpti9hA</recordid><startdate>20111101</startdate><enddate>20111101</enddate><creator>Coulson-Thomas, Vivien J.</creator><creator>Coulson-Thomas, Yvette M.</creator><creator>Gesteira, Tarsis F.</creator><creator>de Paula, Cláudia A. 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A.</au><au>Mader, Ana M.</au><au>Waisberg, Jaques</au><au>Pinhal, Maria A.</au><au>Friedl, Andreas</au><au>Toma, Leny</au><au>Nader, Helena B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Colorectal cancer desmoplastic reaction up-regulates collagen synthesis and restricts cancer cell invasion</atitle><jtitle>Cell and tissue research</jtitle><stitle>Cell Tissue Res</stitle><addtitle>Cell Tissue Res</addtitle><date>2011-11-01</date><risdate>2011</risdate><volume>346</volume><issue>2</issue><spage>223</spage><epage>236</epage><pages>223-236</pages><issn>0302-766X</issn><eissn>1432-0878</eissn><abstract>During cancer cell growth many tumors exhibit various grades of desmoplasia, unorganized production of fibrous or connective tissue, composed mainly of collagen fibers and myofibroblasts. The accumulation of an extracellular matrix (ECM) surrounding tumors directly affects cancer cell proliferation, migration and spread; therefore the study of desmoplasia is of vital importance. Stromal fibroblasts surrounding tumors are activated to myofibroblasts and become the primary producers of ECM during desmoplasia. The composition, density and organization of this ECM accumulation play a major role on the influence desmoplasia has upon tumor cells. In this study, we analyzed desmoplasia
in vivo
in human colorectal carcinoma tissue, detecting an up-regulation of collagen I, collagen IV and collagen V in human colorectal cancer desmoplastic reaction. These components were then analyzed
in vitro
co-cultivating colorectal cancer cells (Caco-2 and HCT116) and fibroblasts utilizing various co-culture techniques. Our findings demonstrate that direct cell-cell contact between fibroblasts and colorectal cancer cells evokes an increase in ECM density, composed of unorganized collagens (I, III, IV and V) and proteoglycans (biglycan, fibromodulin, perlecan and versican). The desmoplastic collagen fibers were thick, with an altered orientation, as well as deposited as bundles. This increased ECM density inhibited the migration and invasion of the colorectal tumor cells in both 2D and 3D co-culture systems. Therefore this study sheds light on a possible restricting role desmoplasia could play in colorectal cancer invasion.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>21987222</pmid><doi>10.1007/s00441-011-1254-y</doi><tpages>14</tpages></addata></record> |
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| subjects | Aged Analysis Biomedical and Life Sciences Biomedicine Cell adhesion & migration Cell growth Cell Line, Tumor Coculture Techniques Collagen Collagen - biosynthesis Collagen - genetics Colorectal cancer Colorectal Neoplasms - genetics Colorectal Neoplasms - metabolism Colorectal Neoplasms - pathology Extracellular Matrix - genetics Extracellular Matrix - metabolism Female Fibroblasts - metabolism Fibroblasts - pathology Gastrointestinal diseases Gene expression Gene Expression Regulation, Neoplastic Human Genetics Humans Male Middle Aged Molecular Medicine Neoplasm Invasiveness Protein synthesis Proteoglycans - metabolism Proteomics Regular Article Stromal Cells - metabolism Stromal Cells - pathology Tumors Up-Regulation |
| title | Colorectal cancer desmoplastic reaction up-regulates collagen synthesis and restricts cancer cell invasion |
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