CD44 Expressed on Cancer‐Associated Fibroblasts Is a Functional Molecule Supporting the Stemness and Drug Resistance of Malignant Cancer Cells in the Tumor Microenvironment
Cells constituting the tumor microenvironment are attractive targets for developing new cancer therapies. Here we show that cancer‐associated fibroblasts (CAFs) support tumor growth in vivo and maintain the stemness of cancer stem/initiating cells in an in vitro model using an established CAF cell l...
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Veröffentlicht in: | Stem cells (Dayton, Ohio) Ohio), 2014-01, Vol.32 (1), p.145-156 |
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description | Cells constituting the tumor microenvironment are attractive targets for developing new cancer therapies. Here we show that cancer‐associated fibroblasts (CAFs) support tumor growth in vivo and maintain the stemness of cancer stem/initiating cells in an in vitro model using an established CAF cell line. We found that CD44 is abundantly expressed on CAFs. This molecule is a cancer stem cell marker in several tumors, but its role in tumorigenesis when expressed by CAFs has not been investigated. It is generally accepted that hypoxic and hyponutritional conditions are triggers of cancer malignancy. We found that CAFs strongly express CD44 in hypoxic and avascular areas in the tumor and that its expression on established CAFs is upregulated under hypoxic and hyponutritional conditions in vitro. In addition, CAF CD44‐positivity in tumor tissues was increased after treatment with inhibitors of angiogenesis. Using cocultures and tumor sphere formation assays, CAFs from wild‐type mice were found to sustain the stemness of cancer stem/initiating cells, while CD44‐deficient CAFs did not. Furthermore, CD44 was involved in malignant cancer cell drug resistance mechanisms. In conclusion, our study suggests that CD44 on CAFs is a functional molecule contributing to the maintenance of cancer stem cell populations in the tumor microenvironment. Stem Cells 2014;32:145–156 |
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Here we show that cancer‐associated fibroblasts (CAFs) support tumor growth in vivo and maintain the stemness of cancer stem/initiating cells in an in vitro model using an established CAF cell line. We found that CD44 is abundantly expressed on CAFs. This molecule is a cancer stem cell marker in several tumors, but its role in tumorigenesis when expressed by CAFs has not been investigated. It is generally accepted that hypoxic and hyponutritional conditions are triggers of cancer malignancy. We found that CAFs strongly express CD44 in hypoxic and avascular areas in the tumor and that its expression on established CAFs is upregulated under hypoxic and hyponutritional conditions in vitro. In addition, CAF CD44‐positivity in tumor tissues was increased after treatment with inhibitors of angiogenesis. Using cocultures and tumor sphere formation assays, CAFs from wild‐type mice were found to sustain the stemness of cancer stem/initiating cells, while CD44‐deficient CAFs did not. Furthermore, CD44 was involved in malignant cancer cell drug resistance mechanisms. In conclusion, our study suggests that CD44 on CAFs is a functional molecule contributing to the maintenance of cancer stem cell populations in the tumor microenvironment. Stem Cells 2014;32:145–156</description><identifier>ISSN: 1066-5099</identifier><identifier>EISSN: 1549-4918</identifier><identifier>DOI: 10.1002/stem.1556</identifier><identifier>PMID: 24395741</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Animal models ; Animals ; Apoptosis - physiology ; Cancer associated fibroblasts ; Carcinoma, Lewis Lung - metabolism ; Carcinoma, Lewis Lung - pathology ; CD44 ; Cell Line, Tumor ; Coculture Techniques ; Drug resistance ; Drug Resistance, Neoplasm ; Female ; Fibroblasts - metabolism ; Fibroblasts - pathology ; HT29 Cells ; Humans ; Hyaluronan Receptors - biosynthesis ; Hyaluronan Receptors - genetics ; Hyaluronan Receptors - metabolism ; Medical research ; Melanoma, Experimental - metabolism ; Melanoma, Experimental - pathology ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Neoplasms - drug therapy ; Neoplasms - metabolism ; Neoplasms - pathology ; Neoplastic Stem Cells - metabolism ; Neoplastic Stem Cells - pathology ; Stem cells ; Stromal Cells - metabolism ; Stromal Cells - pathology ; Tumor Microenvironment ; Tumor stroma</subject><ispartof>Stem cells (Dayton, Ohio), 2014-01, Vol.32 (1), p.145-156</ispartof><rights>2013 AlphaMed Press</rights><rights>2013 AlphaMed Press.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4526-f5a00310350e7ac7e3b00802a8146df3d14e05756696d5069d9d339db130ca503</citedby><cites>FETCH-LOGICAL-c4526-f5a00310350e7ac7e3b00802a8146df3d14e05756696d5069d9d339db130ca503</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24395741$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kinugasa, Yumi</creatorcontrib><creatorcontrib>Matsui, Takahiro</creatorcontrib><creatorcontrib>Takakura, Nobuyuki</creatorcontrib><title>CD44 Expressed on Cancer‐Associated Fibroblasts Is a Functional Molecule Supporting the Stemness and Drug Resistance of Malignant Cancer Cells in the Tumor Microenvironment</title><title>Stem cells (Dayton, Ohio)</title><addtitle>Stem Cells</addtitle><description>Cells constituting the tumor microenvironment are attractive targets for developing new cancer therapies. Here we show that cancer‐associated fibroblasts (CAFs) support tumor growth in vivo and maintain the stemness of cancer stem/initiating cells in an in vitro model using an established CAF cell line. We found that CD44 is abundantly expressed on CAFs. This molecule is a cancer stem cell marker in several tumors, but its role in tumorigenesis when expressed by CAFs has not been investigated. It is generally accepted that hypoxic and hyponutritional conditions are triggers of cancer malignancy. We found that CAFs strongly express CD44 in hypoxic and avascular areas in the tumor and that its expression on established CAFs is upregulated under hypoxic and hyponutritional conditions in vitro. In addition, CAF CD44‐positivity in tumor tissues was increased after treatment with inhibitors of angiogenesis. Using cocultures and tumor sphere formation assays, CAFs from wild‐type mice were found to sustain the stemness of cancer stem/initiating cells, while CD44‐deficient CAFs did not. Furthermore, CD44 was involved in malignant cancer cell drug resistance mechanisms. In conclusion, our study suggests that CD44 on CAFs is a functional molecule contributing to the maintenance of cancer stem cell populations in the tumor microenvironment. Stem Cells 2014;32:145–156</description><subject>Animal models</subject><subject>Animals</subject><subject>Apoptosis - physiology</subject><subject>Cancer associated fibroblasts</subject><subject>Carcinoma, Lewis Lung - metabolism</subject><subject>Carcinoma, Lewis Lung - pathology</subject><subject>CD44</subject><subject>Cell Line, Tumor</subject><subject>Coculture Techniques</subject><subject>Drug resistance</subject><subject>Drug Resistance, Neoplasm</subject><subject>Female</subject><subject>Fibroblasts - metabolism</subject><subject>Fibroblasts - pathology</subject><subject>HT29 Cells</subject><subject>Humans</subject><subject>Hyaluronan Receptors - biosynthesis</subject><subject>Hyaluronan Receptors - genetics</subject><subject>Hyaluronan Receptors - metabolism</subject><subject>Medical research</subject><subject>Melanoma, Experimental - metabolism</subject><subject>Melanoma, Experimental - pathology</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>Neoplasms - drug therapy</subject><subject>Neoplasms - metabolism</subject><subject>Neoplasms - pathology</subject><subject>Neoplastic Stem Cells - metabolism</subject><subject>Neoplastic Stem Cells - pathology</subject><subject>Stem cells</subject><subject>Stromal Cells - metabolism</subject><subject>Stromal Cells - pathology</subject><subject>Tumor Microenvironment</subject><subject>Tumor stroma</subject><issn>1066-5099</issn><issn>1549-4918</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkctu1DAUhiMEoqWw4AWQJTZ0kfY4viReVukMVOoIiQ7ryEmcwZVjB9sBuusj8CQ8FE-C0xlYICGx8kWfP59z_ix7ieEMAxTnIarxDDPGH2XHmFGRU4Grx2kPnOcMhDjKnoVwC4Apq6qn2VFBiWAlxcfZj_qSUrT6NnkVguqRs6iWtlP-5_33ixBcp2VM12vdetcaGWJAVwFJtJ5tF7Wz0qCNM6qbjUI38zQ5H7XdofgpHVNVNlmRtD269PMOfVBBh7jokRvQRhq9s9LGw4-oVsYEpO3D6-08Oo82uvNO2S_aOzsqG59nTwZpgnpxWE-yj-vVtn6XX79_e1VfXOcdZQXPByYBCAbCQJWyKxVpASooZIUp7wfSY6qAlYxzwXsGXPSiJ0T0LSbQSQbkJHuz907efZ5ViM2oQ5fqk1a5OTSYioITAF78DwollBxXCX39F3rrZp9muFAl4UIQIIk63VOp9RC8GprJ61H6uwZDs-TdLHk3S96JfXUwzu2o-j_k74ATcL4Hvmqj7v5tam62q82D8hfpE7ZC</recordid><startdate>201401</startdate><enddate>201401</enddate><creator>Kinugasa, Yumi</creator><creator>Matsui, Takahiro</creator><creator>Takakura, Nobuyuki</creator><general>Oxford University Press</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>7QO</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>201401</creationdate><title>CD44 Expressed on Cancer‐Associated Fibroblasts Is a Functional Molecule Supporting the Stemness and Drug Resistance of Malignant Cancer Cells in the Tumor Microenvironment</title><author>Kinugasa, Yumi ; Matsui, Takahiro ; Takakura, Nobuyuki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4526-f5a00310350e7ac7e3b00802a8146df3d14e05756696d5069d9d339db130ca503</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animal models</topic><topic>Animals</topic><topic>Apoptosis - physiology</topic><topic>Cancer associated fibroblasts</topic><topic>Carcinoma, Lewis Lung - metabolism</topic><topic>Carcinoma, Lewis Lung - pathology</topic><topic>CD44</topic><topic>Cell Line, Tumor</topic><topic>Coculture Techniques</topic><topic>Drug resistance</topic><topic>Drug Resistance, Neoplasm</topic><topic>Female</topic><topic>Fibroblasts - metabolism</topic><topic>Fibroblasts - pathology</topic><topic>HT29 Cells</topic><topic>Humans</topic><topic>Hyaluronan Receptors - biosynthesis</topic><topic>Hyaluronan Receptors - genetics</topic><topic>Hyaluronan Receptors - metabolism</topic><topic>Medical research</topic><topic>Melanoma, Experimental - metabolism</topic><topic>Melanoma, Experimental - pathology</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>Neoplasms - drug therapy</topic><topic>Neoplasms - metabolism</topic><topic>Neoplasms - pathology</topic><topic>Neoplastic Stem Cells - metabolism</topic><topic>Neoplastic Stem Cells - pathology</topic><topic>Stem cells</topic><topic>Stromal Cells - metabolism</topic><topic>Stromal Cells - pathology</topic><topic>Tumor Microenvironment</topic><topic>Tumor stroma</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kinugasa, Yumi</creatorcontrib><creatorcontrib>Matsui, Takahiro</creatorcontrib><creatorcontrib>Takakura, Nobuyuki</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Stem cells (Dayton, Ohio)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kinugasa, Yumi</au><au>Matsui, Takahiro</au><au>Takakura, Nobuyuki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CD44 Expressed on Cancer‐Associated Fibroblasts Is a Functional Molecule Supporting the Stemness and Drug Resistance of Malignant Cancer Cells in the Tumor Microenvironment</atitle><jtitle>Stem cells (Dayton, Ohio)</jtitle><addtitle>Stem Cells</addtitle><date>2014-01</date><risdate>2014</risdate><volume>32</volume><issue>1</issue><spage>145</spage><epage>156</epage><pages>145-156</pages><issn>1066-5099</issn><eissn>1549-4918</eissn><abstract>Cells constituting the tumor microenvironment are attractive targets for developing new cancer therapies. Here we show that cancer‐associated fibroblasts (CAFs) support tumor growth in vivo and maintain the stemness of cancer stem/initiating cells in an in vitro model using an established CAF cell line. We found that CD44 is abundantly expressed on CAFs. This molecule is a cancer stem cell marker in several tumors, but its role in tumorigenesis when expressed by CAFs has not been investigated. It is generally accepted that hypoxic and hyponutritional conditions are triggers of cancer malignancy. We found that CAFs strongly express CD44 in hypoxic and avascular areas in the tumor and that its expression on established CAFs is upregulated under hypoxic and hyponutritional conditions in vitro. In addition, CAF CD44‐positivity in tumor tissues was increased after treatment with inhibitors of angiogenesis. Using cocultures and tumor sphere formation assays, CAFs from wild‐type mice were found to sustain the stemness of cancer stem/initiating cells, while CD44‐deficient CAFs did not. Furthermore, CD44 was involved in malignant cancer cell drug resistance mechanisms. In conclusion, our study suggests that CD44 on CAFs is a functional molecule contributing to the maintenance of cancer stem cell populations in the tumor microenvironment. Stem Cells 2014;32:145–156</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>24395741</pmid><doi>10.1002/stem.1556</doi><tpages>12</tpages></addata></record> |
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subjects | Animal models Animals Apoptosis - physiology Cancer associated fibroblasts Carcinoma, Lewis Lung - metabolism Carcinoma, Lewis Lung - pathology CD44 Cell Line, Tumor Coculture Techniques Drug resistance Drug Resistance, Neoplasm Female Fibroblasts - metabolism Fibroblasts - pathology HT29 Cells Humans Hyaluronan Receptors - biosynthesis Hyaluronan Receptors - genetics Hyaluronan Receptors - metabolism Medical research Melanoma, Experimental - metabolism Melanoma, Experimental - pathology Mice Mice, Inbred C57BL Mice, Knockout Neoplasms - drug therapy Neoplasms - metabolism Neoplasms - pathology Neoplastic Stem Cells - metabolism Neoplastic Stem Cells - pathology Stem cells Stromal Cells - metabolism Stromal Cells - pathology Tumor Microenvironment Tumor stroma |
title | CD44 Expressed on Cancer‐Associated Fibroblasts Is a Functional Molecule Supporting the Stemness and Drug Resistance of Malignant Cancer Cells in the Tumor Microenvironment |
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