Photoimmunotherapy for cancer-associated fibroblasts targeting fibroblast activation protein in human esophageal squamous cell carcinoma
Cancer-associated fibroblasts (CAFs) are strongly implicated in tumor progression, including in the processes of tumorigenesis, invasion, and metastasis. The targeting of CAFs using various therapeutic approaches is a novel treatment strategy; however, the efficacy of such therapies remains limited....
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Veröffentlicht in: | Cancer biology & therapy 2019-09, Vol.20 (9), p.1234-1248 |
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creator | Watanabe, Shinichiro Noma, Kazuhiro Ohara, Toshiaki Kashima, Hajime Sato, Hiroaki Kato, Takuya Urano, Shinichi Katsube, Ryoichi Hashimoto, Yuuri Tazawa, Hiroshi Kagawa, Shunsuke Shirakawa, Yasuhiro Kobayashi, Hisataka Fujiwara, Toshiyoshi |
description | Cancer-associated fibroblasts (CAFs) are strongly implicated in tumor progression, including in the processes of tumorigenesis, invasion, and metastasis. The targeting of CAFs using various therapeutic approaches is a novel treatment strategy; however, the efficacy of such therapies remains limited. Recently, near-infrared photoimmunotherapy (NIR-PIT), which is a novel targeted therapy employing a cell-specific mAb conjugated to a photosensitizer, has been introduced as a new type of phototherapy. In this study, we have developed a novel NIR-PIT technique to target CAFs, by focusing on fibroblast activation protein (FAP), and we evaluate the treatment efficacy in vitro and in vivo. Esophageal carcinoma cells exhibited enhanced activation of fibroblasts, with FAP over-expressed in the cytoplasm and on the cell surface. FAP-IR700-mediated PIT showed induced rapid cell death specifically for those cells in vitro and in vivo, without adverse effects. This novel therapy for CAFs, designed as local control phototherapy, was safe and showed a promising inhibitory effect on FAP
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CAFs. PIT targeting CAFs via the specific marker FAP may be a therapeutic option for CAFs in the tumor microenvironment in the future. |
doi_str_mv | 10.1080/15384047.2019.1617566 |
format | Article |
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+
CAFs. PIT targeting CAFs via the specific marker FAP may be a therapeutic option for CAFs in the tumor microenvironment in the future.</description><identifier>ISSN: 1538-4047</identifier><identifier>EISSN: 1555-8576</identifier><identifier>DOI: 10.1080/15384047.2019.1617566</identifier><identifier>PMID: 31185791</identifier><language>eng</language><publisher>United States: Taylor & Francis</publisher><subject>esophageal cancer ; fibroblast activation protein (FAP) ; mouse model ; near-infrared photoimmunotherapy ; Research Paper ; Tumor microenvironment</subject><ispartof>Cancer biology & therapy, 2019-09, Vol.20 (9), p.1234-1248</ispartof><rights>2019 Taylor & Francis Group, LLC 2019</rights><rights>2019 Taylor & Francis Group, LLC 2019 Taylor & Francis</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c534t-c8cb50989a50abf38912a12c3a0779da6ffff12157d5b8ce39cbb96407c29bed3</citedby><cites>FETCH-LOGICAL-c534t-c8cb50989a50abf38912a12c3a0779da6ffff12157d5b8ce39cbb96407c29bed3</cites><orcidid>0000-0002-5584-3908</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6741582/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6741582/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,724,777,781,882,27905,27906,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31185791$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Watanabe, Shinichiro</creatorcontrib><creatorcontrib>Noma, Kazuhiro</creatorcontrib><creatorcontrib>Ohara, Toshiaki</creatorcontrib><creatorcontrib>Kashima, Hajime</creatorcontrib><creatorcontrib>Sato, Hiroaki</creatorcontrib><creatorcontrib>Kato, Takuya</creatorcontrib><creatorcontrib>Urano, Shinichi</creatorcontrib><creatorcontrib>Katsube, Ryoichi</creatorcontrib><creatorcontrib>Hashimoto, Yuuri</creatorcontrib><creatorcontrib>Tazawa, Hiroshi</creatorcontrib><creatorcontrib>Kagawa, Shunsuke</creatorcontrib><creatorcontrib>Shirakawa, Yasuhiro</creatorcontrib><creatorcontrib>Kobayashi, Hisataka</creatorcontrib><creatorcontrib>Fujiwara, Toshiyoshi</creatorcontrib><title>Photoimmunotherapy for cancer-associated fibroblasts targeting fibroblast activation protein in human esophageal squamous cell carcinoma</title><title>Cancer biology & therapy</title><addtitle>Cancer Biol Ther</addtitle><description>Cancer-associated fibroblasts (CAFs) are strongly implicated in tumor progression, including in the processes of tumorigenesis, invasion, and metastasis. The targeting of CAFs using various therapeutic approaches is a novel treatment strategy; however, the efficacy of such therapies remains limited. Recently, near-infrared photoimmunotherapy (NIR-PIT), which is a novel targeted therapy employing a cell-specific mAb conjugated to a photosensitizer, has been introduced as a new type of phototherapy. In this study, we have developed a novel NIR-PIT technique to target CAFs, by focusing on fibroblast activation protein (FAP), and we evaluate the treatment efficacy in vitro and in vivo. Esophageal carcinoma cells exhibited enhanced activation of fibroblasts, with FAP over-expressed in the cytoplasm and on the cell surface. FAP-IR700-mediated PIT showed induced rapid cell death specifically for those cells in vitro and in vivo, without adverse effects. This novel therapy for CAFs, designed as local control phototherapy, was safe and showed a promising inhibitory effect on FAP
+
CAFs. PIT targeting CAFs via the specific marker FAP may be a therapeutic option for CAFs in the tumor microenvironment in the future.</description><subject>esophageal cancer</subject><subject>fibroblast activation protein (FAP)</subject><subject>mouse model</subject><subject>near-infrared photoimmunotherapy</subject><subject>Research Paper</subject><subject>Tumor microenvironment</subject><issn>1538-4047</issn><issn>1555-8576</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kVFv1SAUgBujcXP6EzQ8-tIr0ELhxWgWN02W6IM-k1NKbzEFOqBb7j_wZ0tz75b5IiHhBL5zDidfVb0leEewwB8Ia0SL225HMZE7wknHOH9WnRPGWC1Yx59vcSPqDTqrXqX0G2PaUS5fVmcNIQWR5Lz682MKOVjnVh_yZCIsBzSGiDR4bWINKQVtIZsBjbaPoZ8h5YQyxL3J1u-f3CLQ2d5BtsGjJYZsrEdlT6sDj0wKywR7AzNKtyu4sCakzTyXPlFbHxy8rl6MMCfz5nReVL-uvvy8_FrffL_-dvn5ptasaXOthe4ZlkICw9CPjZCEAqG6Adx1cgA-lkUoYd3AeqFNI3XfS97iTlPZm6G5qD4e6y5r78ygjc8RZrVE6yAeVACr_n3xdlL7cKd41xImaCnw_lQghtvVpKycTdss4E0ZS1HKRUNaKklB2RHVMaQUzfjYhmC1WVQPFtVmUZ0slrx3T__4mPWgrQCfjoD1RZaD-xDnQWU4zCGOsaizqcD_7fEX7Iiyag</recordid><startdate>20190902</startdate><enddate>20190902</enddate><creator>Watanabe, Shinichiro</creator><creator>Noma, Kazuhiro</creator><creator>Ohara, Toshiaki</creator><creator>Kashima, Hajime</creator><creator>Sato, Hiroaki</creator><creator>Kato, Takuya</creator><creator>Urano, Shinichi</creator><creator>Katsube, Ryoichi</creator><creator>Hashimoto, Yuuri</creator><creator>Tazawa, Hiroshi</creator><creator>Kagawa, Shunsuke</creator><creator>Shirakawa, Yasuhiro</creator><creator>Kobayashi, Hisataka</creator><creator>Fujiwara, Toshiyoshi</creator><general>Taylor & Francis</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-5584-3908</orcidid></search><sort><creationdate>20190902</creationdate><title>Photoimmunotherapy for cancer-associated fibroblasts targeting fibroblast activation protein in human esophageal squamous cell carcinoma</title><author>Watanabe, Shinichiro ; Noma, Kazuhiro ; Ohara, Toshiaki ; Kashima, Hajime ; Sato, Hiroaki ; Kato, Takuya ; Urano, Shinichi ; Katsube, Ryoichi ; Hashimoto, Yuuri ; Tazawa, Hiroshi ; Kagawa, Shunsuke ; Shirakawa, Yasuhiro ; Kobayashi, Hisataka ; Fujiwara, Toshiyoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c534t-c8cb50989a50abf38912a12c3a0779da6ffff12157d5b8ce39cbb96407c29bed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>esophageal cancer</topic><topic>fibroblast activation protein (FAP)</topic><topic>mouse model</topic><topic>near-infrared photoimmunotherapy</topic><topic>Research Paper</topic><topic>Tumor microenvironment</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Watanabe, Shinichiro</creatorcontrib><creatorcontrib>Noma, Kazuhiro</creatorcontrib><creatorcontrib>Ohara, Toshiaki</creatorcontrib><creatorcontrib>Kashima, Hajime</creatorcontrib><creatorcontrib>Sato, Hiroaki</creatorcontrib><creatorcontrib>Kato, Takuya</creatorcontrib><creatorcontrib>Urano, Shinichi</creatorcontrib><creatorcontrib>Katsube, Ryoichi</creatorcontrib><creatorcontrib>Hashimoto, Yuuri</creatorcontrib><creatorcontrib>Tazawa, Hiroshi</creatorcontrib><creatorcontrib>Kagawa, Shunsuke</creatorcontrib><creatorcontrib>Shirakawa, Yasuhiro</creatorcontrib><creatorcontrib>Kobayashi, Hisataka</creatorcontrib><creatorcontrib>Fujiwara, Toshiyoshi</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancer biology & therapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Watanabe, Shinichiro</au><au>Noma, Kazuhiro</au><au>Ohara, Toshiaki</au><au>Kashima, Hajime</au><au>Sato, Hiroaki</au><au>Kato, Takuya</au><au>Urano, Shinichi</au><au>Katsube, Ryoichi</au><au>Hashimoto, Yuuri</au><au>Tazawa, Hiroshi</au><au>Kagawa, Shunsuke</au><au>Shirakawa, Yasuhiro</au><au>Kobayashi, Hisataka</au><au>Fujiwara, Toshiyoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Photoimmunotherapy for cancer-associated fibroblasts targeting fibroblast activation protein in human esophageal squamous cell carcinoma</atitle><jtitle>Cancer biology & therapy</jtitle><addtitle>Cancer Biol Ther</addtitle><date>2019-09-02</date><risdate>2019</risdate><volume>20</volume><issue>9</issue><spage>1234</spage><epage>1248</epage><pages>1234-1248</pages><issn>1538-4047</issn><eissn>1555-8576</eissn><abstract>Cancer-associated fibroblasts (CAFs) are strongly implicated in tumor progression, including in the processes of tumorigenesis, invasion, and metastasis. The targeting of CAFs using various therapeutic approaches is a novel treatment strategy; however, the efficacy of such therapies remains limited. Recently, near-infrared photoimmunotherapy (NIR-PIT), which is a novel targeted therapy employing a cell-specific mAb conjugated to a photosensitizer, has been introduced as a new type of phototherapy. In this study, we have developed a novel NIR-PIT technique to target CAFs, by focusing on fibroblast activation protein (FAP), and we evaluate the treatment efficacy in vitro and in vivo. Esophageal carcinoma cells exhibited enhanced activation of fibroblasts, with FAP over-expressed in the cytoplasm and on the cell surface. FAP-IR700-mediated PIT showed induced rapid cell death specifically for those cells in vitro and in vivo, without adverse effects. This novel therapy for CAFs, designed as local control phototherapy, was safe and showed a promising inhibitory effect on FAP
+
CAFs. PIT targeting CAFs via the specific marker FAP may be a therapeutic option for CAFs in the tumor microenvironment in the future.</abstract><cop>United States</cop><pub>Taylor & Francis</pub><pmid>31185791</pmid><doi>10.1080/15384047.2019.1617566</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0002-5584-3908</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | esophageal cancer fibroblast activation protein (FAP) mouse model near-infrared photoimmunotherapy Research Paper Tumor microenvironment |
title | Photoimmunotherapy for cancer-associated fibroblasts targeting fibroblast activation protein in human esophageal squamous cell carcinoma |
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