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REG I enhances chemo‐ and radiosensitivity in squamous cell esophageal cancer cells
Identification of reliable markers of chemo‐ and radiosensitivity and the key molecules that enhance the susceptibility of squamous esophageal cancer cells to anticancer treatments would be highly desirable. To test whether regenerating gene (REG) I expression enhances chemo‐ and radiosensitivity in...
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Published in: | Cancer science 2008-12, Vol.99 (12), p.2491-2495 |
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creator | Hayashi, Kaori Motoyama, Satoru Koyota, Souichi Koizumi, Yukio Wang, Jingshu Takasawa, Shin Itaya‐Hironaka, Asako Sakuramoto‐Tsuchida, Sumiyo Maruyama, Kiyotomi Saito, Hajime Minamiya, Yoshihiro Ogawa, Jun‐ichi Sugiyama, Toshihiro |
description | Identification of reliable markers of chemo‐ and radiosensitivity and the key molecules that enhance the susceptibility of squamous esophageal cancer cells to anticancer treatments would be highly desirable. To test whether regenerating gene (REG) I expression enhances chemo‐ and radiosensitivity in esophageal squamous cell carcinoma cells, we used MTT (3‐[4,5‐dimethylthiazol‐2‐yl]‐2,5‐diphenyltetrazolium bromide) assays to compare the chemo‐ and radiosensitivities of untransfected TE‐5 and TE‐9 cells with those of cells stably transfected with REG Iα and Iβ. We then used flow cytometry to determine whether REG I expression alters cell cycle progression. No REG I mRNA or protein were detected in untransfected TE‐5 and TE‐9 cells. Transfection with REG Iα and Iβ led to strong expression of both REG I mRNA and protein in TE‐5 and TE‐9 cells, which in turn led to significant increases in both chemo‐ and radiosensitivity. Cell cycle progression was unaffected by REG I expression. REG I thus appears to enhance the chemo‐ and radiosensitivity of squamous esophageal cancer cells, which suggests that it may be a useful target for improved and more individualized treatments for patients with esophageal squamous cell carcinoma. (Cancer Sci 2008; 99: 2491–2495) |
doi_str_mv | 10.1111/j.1349-7006.2008.00980.x |
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To test whether regenerating gene (REG) I expression enhances chemo‐ and radiosensitivity in esophageal squamous cell carcinoma cells, we used MTT (3‐[4,5‐dimethylthiazol‐2‐yl]‐2,5‐diphenyltetrazolium bromide) assays to compare the chemo‐ and radiosensitivities of untransfected TE‐5 and TE‐9 cells with those of cells stably transfected with REG Iα and Iβ. We then used flow cytometry to determine whether REG I expression alters cell cycle progression. No REG I mRNA or protein were detected in untransfected TE‐5 and TE‐9 cells. Transfection with REG Iα and Iβ led to strong expression of both REG I mRNA and protein in TE‐5 and TE‐9 cells, which in turn led to significant increases in both chemo‐ and radiosensitivity. Cell cycle progression was unaffected by REG I expression. REG I thus appears to enhance the chemo‐ and radiosensitivity of squamous esophageal cancer cells, which suggests that it may be a useful target for improved and more individualized treatments for patients with esophageal squamous cell carcinoma. (Cancer Sci 2008; 99: 2491–2495)</description><identifier>ISSN: 1347-9032</identifier><identifier>ISSN: 1349-7006</identifier><identifier>EISSN: 1349-7006</identifier><identifier>DOI: 10.1111/j.1349-7006.2008.00980.x</identifier><identifier>PMID: 19032369</identifier><language>eng</language><publisher>Melbourne, Australia: Blackwell Publishing Asia</publisher><subject>Antimetabolites, Antineoplastic - metabolism ; Antimetabolites, Antineoplastic - therapeutic use ; Biological and medical sciences ; Carcinoma, Squamous Cell - drug therapy ; Carcinoma, Squamous Cell - genetics ; Carcinoma, Squamous Cell - metabolism ; Carcinoma, Squamous Cell - pathology ; Carcinoma, Squamous Cell - radiotherapy ; Cell Line, Tumor ; Cell Proliferation - drug effects ; Cell Proliferation - radiation effects ; Dose-Response Relationship, Radiation ; Esophageal Neoplasms - drug therapy ; Esophageal Neoplasms - genetics ; Esophageal Neoplasms - metabolism ; Esophageal Neoplasms - pathology ; Esophageal Neoplasms - radiotherapy ; Fluorouracil - metabolism ; Fluorouracil - therapeutic use ; Formazans - metabolism ; Humans ; Lithostathine - genetics ; Lithostathine - metabolism ; Medical sciences ; Original ; Proteins - metabolism ; Radiation Tolerance - genetics ; RNA, Messenger - metabolism ; Tetrazolium Salts - metabolism ; Transfection ; Tumors</subject><ispartof>Cancer science, 2008-12, Vol.99 (12), p.2491-2495</ispartof><rights>2008 Japanese Cancer Association</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c6520-4cfd4a2734d92e766e9398c2df201e9bfb4c856cf8e2989b0dfabd4610877c4c3</citedby><cites>FETCH-LOGICAL-c6520-4cfd4a2734d92e766e9398c2df201e9bfb4c856cf8e2989b0dfabd4610877c4c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11159624/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11159624/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,11561,27923,27924,37012,46051,46475,53790,53792</link.rule.ids><linktorsrc>$$Uhttps://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1349-7006.2008.00980.x$$EView_record_in_Wiley-Blackwell$$FView_record_in_$$GWiley-Blackwell</linktorsrc><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20954934$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19032369$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hayashi, Kaori</creatorcontrib><creatorcontrib>Motoyama, Satoru</creatorcontrib><creatorcontrib>Koyota, Souichi</creatorcontrib><creatorcontrib>Koizumi, Yukio</creatorcontrib><creatorcontrib>Wang, Jingshu</creatorcontrib><creatorcontrib>Takasawa, Shin</creatorcontrib><creatorcontrib>Itaya‐Hironaka, Asako</creatorcontrib><creatorcontrib>Sakuramoto‐Tsuchida, Sumiyo</creatorcontrib><creatorcontrib>Maruyama, Kiyotomi</creatorcontrib><creatorcontrib>Saito, Hajime</creatorcontrib><creatorcontrib>Minamiya, Yoshihiro</creatorcontrib><creatorcontrib>Ogawa, Jun‐ichi</creatorcontrib><creatorcontrib>Sugiyama, Toshihiro</creatorcontrib><title>REG I enhances chemo‐ and radiosensitivity in squamous cell esophageal cancer cells</title><title>Cancer science</title><addtitle>Cancer Sci</addtitle><description>Identification of reliable markers of chemo‐ and radiosensitivity and the key molecules that enhance the susceptibility of squamous esophageal cancer cells to anticancer treatments would be highly desirable. To test whether regenerating gene (REG) I expression enhances chemo‐ and radiosensitivity in esophageal squamous cell carcinoma cells, we used MTT (3‐[4,5‐dimethylthiazol‐2‐yl]‐2,5‐diphenyltetrazolium bromide) assays to compare the chemo‐ and radiosensitivities of untransfected TE‐5 and TE‐9 cells with those of cells stably transfected with REG Iα and Iβ. We then used flow cytometry to determine whether REG I expression alters cell cycle progression. No REG I mRNA or protein were detected in untransfected TE‐5 and TE‐9 cells. Transfection with REG Iα and Iβ led to strong expression of both REG I mRNA and protein in TE‐5 and TE‐9 cells, which in turn led to significant increases in both chemo‐ and radiosensitivity. Cell cycle progression was unaffected by REG I expression. REG I thus appears to enhance the chemo‐ and radiosensitivity of squamous esophageal cancer cells, which suggests that it may be a useful target for improved and more individualized treatments for patients with esophageal squamous cell carcinoma. (Cancer Sci 2008; 99: 2491–2495)</description><subject>Antimetabolites, Antineoplastic - metabolism</subject><subject>Antimetabolites, Antineoplastic - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Carcinoma, Squamous Cell - drug therapy</subject><subject>Carcinoma, Squamous Cell - genetics</subject><subject>Carcinoma, Squamous Cell - metabolism</subject><subject>Carcinoma, Squamous Cell - pathology</subject><subject>Carcinoma, Squamous Cell - radiotherapy</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation - drug effects</subject><subject>Cell Proliferation - radiation effects</subject><subject>Dose-Response Relationship, Radiation</subject><subject>Esophageal Neoplasms - drug therapy</subject><subject>Esophageal Neoplasms - genetics</subject><subject>Esophageal Neoplasms - metabolism</subject><subject>Esophageal Neoplasms - pathology</subject><subject>Esophageal Neoplasms - radiotherapy</subject><subject>Fluorouracil - metabolism</subject><subject>Fluorouracil - therapeutic use</subject><subject>Formazans - metabolism</subject><subject>Humans</subject><subject>Lithostathine - genetics</subject><subject>Lithostathine - metabolism</subject><subject>Medical sciences</subject><subject>Original</subject><subject>Proteins - metabolism</subject><subject>Radiation Tolerance - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Tetrazolium Salts - metabolism</subject><subject>Transfection</subject><subject>Tumors</subject><issn>1347-9032</issn><issn>1349-7006</issn><issn>1349-7006</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqNkc9uEzEQxi1ERUvhFZAvcNtl1uv12hISqqJSKlVCKvRseb2zjaP9k9pJ29x4hD5jnwQ7iQKcwBdbM7_5PDMfIbSAvIjn4yIvSq6yGkDkDEDmAEpC_viCnBwSL7fvOlNQsmPyOoQFQCm44q_IcZGCpVAn5Ob6_IJeUhznZrQYqJ3jMD3_fKJmbKk3rZsCjsGt3L1bbagbabhbm2FaRxL7nmKYlnNzi6anNgn4bTi8IUed6QO-3d-n5ObL-Y_Z1-zq28Xl7Owqs6JikHHbtdywuuStYlgLgapU0rK2Y1CgarqGW1kJ20lkSqoG2s40LRcFyLq23Jan5PNOd7luBmwtjitver30bjB-oyfj9N-Z0c317XSv4xIrJRiPCh_2Cn66W2NY6cGFNIMZMU6phZJSslr8E2SQKFZFUO5A66cQPHaHdgpI_xZ6oZNJOpmkk3t6655-jKXv_hznd-Hergi83wMmWNN3Pu7chQPHQFVclWmqTzvuwfW4-e8G9Ozse3yUvwD2_7eC</recordid><startdate>200812</startdate><enddate>200812</enddate><creator>Hayashi, Kaori</creator><creator>Motoyama, Satoru</creator><creator>Koyota, Souichi</creator><creator>Koizumi, Yukio</creator><creator>Wang, Jingshu</creator><creator>Takasawa, Shin</creator><creator>Itaya‐Hironaka, Asako</creator><creator>Sakuramoto‐Tsuchida, Sumiyo</creator><creator>Maruyama, Kiyotomi</creator><creator>Saito, Hajime</creator><creator>Minamiya, Yoshihiro</creator><creator>Ogawa, Jun‐ichi</creator><creator>Sugiyama, Toshihiro</creator><general>Blackwell Publishing Asia</general><general>Blackwell</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><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>200812</creationdate><title>REG I enhances chemo‐ and radiosensitivity in squamous cell esophageal cancer cells</title><author>Hayashi, Kaori ; Motoyama, Satoru ; Koyota, Souichi ; Koizumi, Yukio ; Wang, Jingshu ; Takasawa, Shin ; Itaya‐Hironaka, Asako ; Sakuramoto‐Tsuchida, Sumiyo ; Maruyama, Kiyotomi ; Saito, Hajime ; Minamiya, Yoshihiro ; Ogawa, Jun‐ichi ; Sugiyama, Toshihiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6520-4cfd4a2734d92e766e9398c2df201e9bfb4c856cf8e2989b0dfabd4610877c4c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Antimetabolites, Antineoplastic - metabolism</topic><topic>Antimetabolites, Antineoplastic - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Carcinoma, Squamous Cell - drug therapy</topic><topic>Carcinoma, Squamous Cell - genetics</topic><topic>Carcinoma, Squamous Cell - metabolism</topic><topic>Carcinoma, Squamous Cell - pathology</topic><topic>Carcinoma, Squamous Cell - radiotherapy</topic><topic>Cell Line, Tumor</topic><topic>Cell Proliferation - drug effects</topic><topic>Cell Proliferation - radiation effects</topic><topic>Dose-Response Relationship, Radiation</topic><topic>Esophageal Neoplasms - drug therapy</topic><topic>Esophageal Neoplasms - genetics</topic><topic>Esophageal Neoplasms - metabolism</topic><topic>Esophageal Neoplasms - pathology</topic><topic>Esophageal Neoplasms - radiotherapy</topic><topic>Fluorouracil - metabolism</topic><topic>Fluorouracil - therapeutic use</topic><topic>Formazans - metabolism</topic><topic>Humans</topic><topic>Lithostathine - genetics</topic><topic>Lithostathine - metabolism</topic><topic>Medical sciences</topic><topic>Original</topic><topic>Proteins - metabolism</topic><topic>Radiation Tolerance - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>Tetrazolium Salts - metabolism</topic><topic>Transfection</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hayashi, Kaori</creatorcontrib><creatorcontrib>Motoyama, Satoru</creatorcontrib><creatorcontrib>Koyota, Souichi</creatorcontrib><creatorcontrib>Koizumi, Yukio</creatorcontrib><creatorcontrib>Wang, Jingshu</creatorcontrib><creatorcontrib>Takasawa, Shin</creatorcontrib><creatorcontrib>Itaya‐Hironaka, Asako</creatorcontrib><creatorcontrib>Sakuramoto‐Tsuchida, Sumiyo</creatorcontrib><creatorcontrib>Maruyama, Kiyotomi</creatorcontrib><creatorcontrib>Saito, Hajime</creatorcontrib><creatorcontrib>Minamiya, Yoshihiro</creatorcontrib><creatorcontrib>Ogawa, Jun‐ichi</creatorcontrib><creatorcontrib>Sugiyama, Toshihiro</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><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancer science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Hayashi, Kaori</au><au>Motoyama, Satoru</au><au>Koyota, Souichi</au><au>Koizumi, Yukio</au><au>Wang, Jingshu</au><au>Takasawa, Shin</au><au>Itaya‐Hironaka, Asako</au><au>Sakuramoto‐Tsuchida, Sumiyo</au><au>Maruyama, Kiyotomi</au><au>Saito, Hajime</au><au>Minamiya, Yoshihiro</au><au>Ogawa, Jun‐ichi</au><au>Sugiyama, Toshihiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>REG I enhances chemo‐ and radiosensitivity in squamous cell esophageal cancer cells</atitle><jtitle>Cancer science</jtitle><addtitle>Cancer Sci</addtitle><date>2008-12</date><risdate>2008</risdate><volume>99</volume><issue>12</issue><spage>2491</spage><epage>2495</epage><pages>2491-2495</pages><issn>1347-9032</issn><issn>1349-7006</issn><eissn>1349-7006</eissn><abstract>Identification of reliable markers of chemo‐ and radiosensitivity and the key molecules that enhance the susceptibility of squamous esophageal cancer cells to anticancer treatments would be highly desirable. To test whether regenerating gene (REG) I expression enhances chemo‐ and radiosensitivity in esophageal squamous cell carcinoma cells, we used MTT (3‐[4,5‐dimethylthiazol‐2‐yl]‐2,5‐diphenyltetrazolium bromide) assays to compare the chemo‐ and radiosensitivities of untransfected TE‐5 and TE‐9 cells with those of cells stably transfected with REG Iα and Iβ. We then used flow cytometry to determine whether REG I expression alters cell cycle progression. No REG I mRNA or protein were detected in untransfected TE‐5 and TE‐9 cells. Transfection with REG Iα and Iβ led to strong expression of both REG I mRNA and protein in TE‐5 and TE‐9 cells, which in turn led to significant increases in both chemo‐ and radiosensitivity. Cell cycle progression was unaffected by REG I expression. REG I thus appears to enhance the chemo‐ and radiosensitivity of squamous esophageal cancer cells, which suggests that it may be a useful target for improved and more individualized treatments for patients with esophageal squamous cell carcinoma. (Cancer Sci 2008; 99: 2491–2495)</abstract><cop>Melbourne, Australia</cop><pub>Blackwell Publishing Asia</pub><pmid>19032369</pmid><doi>10.1111/j.1349-7006.2008.00980.x</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antimetabolites, Antineoplastic - metabolism Antimetabolites, Antineoplastic - therapeutic use Biological and medical sciences Carcinoma, Squamous Cell - drug therapy Carcinoma, Squamous Cell - genetics Carcinoma, Squamous Cell - metabolism Carcinoma, Squamous Cell - pathology Carcinoma, Squamous Cell - radiotherapy Cell Line, Tumor Cell Proliferation - drug effects Cell Proliferation - radiation effects Dose-Response Relationship, Radiation Esophageal Neoplasms - drug therapy Esophageal Neoplasms - genetics Esophageal Neoplasms - metabolism Esophageal Neoplasms - pathology Esophageal Neoplasms - radiotherapy Fluorouracil - metabolism Fluorouracil - therapeutic use Formazans - metabolism Humans Lithostathine - genetics Lithostathine - metabolism Medical sciences Original Proteins - metabolism Radiation Tolerance - genetics RNA, Messenger - metabolism Tetrazolium Salts - metabolism Transfection Tumors |
title | REG I enhances chemo‐ and radiosensitivity in squamous cell esophageal cancer cells |
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