Optimization of hyperthermia and dendritic cell immunotherapy for squamous cell carcinoma
The aims of this study were to explore the feasibility of a novel combination therapy comprising hyperthermia (HT) and dendritic cell (DC) application for squamous cell carcinoma (SCC), and to optimize the conditions of this therapy. In vitro, the correlation between maturation of DCs by co-culture...
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Veröffentlicht in: | Oncology reports 2011-06, Vol.25 (6), p.1525-1532 |
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creator | MATSUMOTO, Koushi YAMAMOTO, Noriyuki UEDA, Minoru HAGIWARA, Sumitaka SAITO, Masaki FURUE, Hiroki SHIGETOMI, Toshio NARITA, Yuji MITSUDO, Kenji TOHNAI, Iwai KOBAYASHI, Takeshi |
description | The aims of this study were to explore the feasibility of a novel combination therapy comprising hyperthermia (HT) and dendritic cell (DC) application for squamous cell carcinoma (SCC), and to optimize the conditions of this therapy. In vitro, the correlation between maturation of DCs by co-culture with SCCVII cells and HT was investigated. DCs did not mature in simple HT (43 °C for 30 min) with SCCVII cells. On the other hand, DC maturation occurred in additional mild HT (mHT: 41 °C for 30 min) with simple HT. To assess whether additional mHT was effective, in vivo combined treatment was performed using tumor-bearing C3H/HeJ mice. A more suppressive effect of tumor growth was observed, and cytotoxic T cell infiltration was significantly increased by adding mHT compared to conventional only simple HT with DCs. These phenomena also occurred in non-treated contralateral tumors as well as treated ones. Our data suggest that the combination of 43 °C preheated simple HT SCCVII tumors and additional 41 °C heat mHT promotes DC maturation, resulting in suppression of tumor growth systemically and lifetime prolongation in mice. A three-step process of additional mHT after local HT and intratumoral immature DC (iDC) injection could be a more effective and novel method for the treatment of SCC. |
doi_str_mv | 10.3892/or.2011.1232 |
format | Article |
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In vitro, the correlation between maturation of DCs by co-culture with SCCVII cells and HT was investigated. DCs did not mature in simple HT (43 °C for 30 min) with SCCVII cells. On the other hand, DC maturation occurred in additional mild HT (mHT: 41 °C for 30 min) with simple HT. To assess whether additional mHT was effective, in vivo combined treatment was performed using tumor-bearing C3H/HeJ mice. A more suppressive effect of tumor growth was observed, and cytotoxic T cell infiltration was significantly increased by adding mHT compared to conventional only simple HT with DCs. These phenomena also occurred in non-treated contralateral tumors as well as treated ones. Our data suggest that the combination of 43 °C preheated simple HT SCCVII tumors and additional 41 °C heat mHT promotes DC maturation, resulting in suppression of tumor growth systemically and lifetime prolongation in mice. A three-step process of additional mHT after local HT and intratumoral immature DC (iDC) injection could be a more effective and novel method for the treatment of SCC.</description><identifier>ISSN: 1021-335X</identifier><identifier>EISSN: 1791-2431</identifier><identifier>DOI: 10.3892/or.2011.1232</identifier><identifier>PMID: 21455579</identifier><language>eng</language><publisher>Athens: Spandidos</publisher><subject>Animals ; Biological and medical sciences ; Blotting, Western ; Carcinoma, Squamous Cell - therapy ; Dendritic Cells - transplantation ; Dermatology ; Female ; Fluorescent Antibody Technique ; HSP70 Heat-Shock Proteins - biosynthesis ; Hyperthermia, Induced ; Immunotherapy - methods ; Medical sciences ; Mice ; Mice, Inbred C3H ; Tumors ; Tumors of the skin and soft tissue. Premalignant lesions</subject><ispartof>Oncology reports, 2011-06, Vol.25 (6), p.1525-1532</ispartof><rights>2015 INIST-CNRS</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c358t-e9ebb44ede4d85c652f91692a3e3327b382b2e0890da68fec08bc2931bdbd3343</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24141918$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21455579$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>MATSUMOTO, Koushi</creatorcontrib><creatorcontrib>YAMAMOTO, Noriyuki</creatorcontrib><creatorcontrib>UEDA, Minoru</creatorcontrib><creatorcontrib>HAGIWARA, Sumitaka</creatorcontrib><creatorcontrib>SAITO, Masaki</creatorcontrib><creatorcontrib>FURUE, Hiroki</creatorcontrib><creatorcontrib>SHIGETOMI, Toshio</creatorcontrib><creatorcontrib>NARITA, Yuji</creatorcontrib><creatorcontrib>MITSUDO, Kenji</creatorcontrib><creatorcontrib>TOHNAI, Iwai</creatorcontrib><creatorcontrib>KOBAYASHI, Takeshi</creatorcontrib><title>Optimization of hyperthermia and dendritic cell immunotherapy for squamous cell carcinoma</title><title>Oncology reports</title><addtitle>Oncol Rep</addtitle><description>The aims of this study were to explore the feasibility of a novel combination therapy comprising hyperthermia (HT) and dendritic cell (DC) application for squamous cell carcinoma (SCC), and to optimize the conditions of this therapy. In vitro, the correlation between maturation of DCs by co-culture with SCCVII cells and HT was investigated. DCs did not mature in simple HT (43 °C for 30 min) with SCCVII cells. On the other hand, DC maturation occurred in additional mild HT (mHT: 41 °C for 30 min) with simple HT. To assess whether additional mHT was effective, in vivo combined treatment was performed using tumor-bearing C3H/HeJ mice. A more suppressive effect of tumor growth was observed, and cytotoxic T cell infiltration was significantly increased by adding mHT compared to conventional only simple HT with DCs. These phenomena also occurred in non-treated contralateral tumors as well as treated ones. Our data suggest that the combination of 43 °C preheated simple HT SCCVII tumors and additional 41 °C heat mHT promotes DC maturation, resulting in suppression of tumor growth systemically and lifetime prolongation in mice. A three-step process of additional mHT after local HT and intratumoral immature DC (iDC) injection could be a more effective and novel method for the treatment of SCC.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Blotting, Western</subject><subject>Carcinoma, Squamous Cell - therapy</subject><subject>Dendritic Cells - transplantation</subject><subject>Dermatology</subject><subject>Female</subject><subject>Fluorescent Antibody Technique</subject><subject>HSP70 Heat-Shock Proteins - biosynthesis</subject><subject>Hyperthermia, Induced</subject><subject>Immunotherapy - methods</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred C3H</subject><subject>Tumors</subject><subject>Tumors of the skin and soft tissue. Premalignant lesions</subject><issn>1021-335X</issn><issn>1791-2431</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpF0MtLxDAQBvAgirs-bp6lF_Fi1yTTR3KUxRcs7EVBTyFNUjbSNN2kPax_vS276mkG5sfH8CF0RfACGKf3PiwoJmRBKNAjNCclJynNgByPO6YkBcg_Zugsxi-MaYkLfopmlGR5npd8jj7XXW-d_Za99W3i62Sz60zoNyY4KxPZ6kSbVgfbW5Uo0zSJdW5o_QRkt0tqH5K4HaTzQ9zflQzKtt7JC3RSyyaay8M8R-9Pj2_Ll3S1fn5dPqxSBTnrU8NNVWWZ0SbTLFdFTmtOCk4lGABaVsBoRQ1mHGtZsNoozCpFOZBKVxogg3N0u8_tgt8OJvbC2Ti9IlszfiVYQUsOBYdR3u2lCj7GYGrRBetk2AmCxdSl8EFMXYqpy5FfH4KHyhn9h3_LG8HNAcioZFMH2Sob_11GMsIJgx9piH31</recordid><startdate>20110601</startdate><enddate>20110601</enddate><creator>MATSUMOTO, Koushi</creator><creator>YAMAMOTO, Noriyuki</creator><creator>UEDA, Minoru</creator><creator>HAGIWARA, Sumitaka</creator><creator>SAITO, Masaki</creator><creator>FURUE, Hiroki</creator><creator>SHIGETOMI, Toshio</creator><creator>NARITA, Yuji</creator><creator>MITSUDO, Kenji</creator><creator>TOHNAI, Iwai</creator><creator>KOBAYASHI, Takeshi</creator><general>Spandidos</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>7X8</scope></search><sort><creationdate>20110601</creationdate><title>Optimization of hyperthermia and dendritic cell immunotherapy for squamous cell carcinoma</title><author>MATSUMOTO, Koushi ; YAMAMOTO, Noriyuki ; UEDA, Minoru ; HAGIWARA, Sumitaka ; SAITO, Masaki ; FURUE, Hiroki ; SHIGETOMI, Toshio ; NARITA, Yuji ; MITSUDO, Kenji ; TOHNAI, Iwai ; KOBAYASHI, Takeshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c358t-e9ebb44ede4d85c652f91692a3e3327b382b2e0890da68fec08bc2931bdbd3343</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Blotting, Western</topic><topic>Carcinoma, Squamous Cell - therapy</topic><topic>Dendritic Cells - transplantation</topic><topic>Dermatology</topic><topic>Female</topic><topic>Fluorescent Antibody Technique</topic><topic>HSP70 Heat-Shock Proteins - biosynthesis</topic><topic>Hyperthermia, Induced</topic><topic>Immunotherapy - methods</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred C3H</topic><topic>Tumors</topic><topic>Tumors of the skin and soft tissue. 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In vitro, the correlation between maturation of DCs by co-culture with SCCVII cells and HT was investigated. DCs did not mature in simple HT (43 °C for 30 min) with SCCVII cells. On the other hand, DC maturation occurred in additional mild HT (mHT: 41 °C for 30 min) with simple HT. To assess whether additional mHT was effective, in vivo combined treatment was performed using tumor-bearing C3H/HeJ mice. A more suppressive effect of tumor growth was observed, and cytotoxic T cell infiltration was significantly increased by adding mHT compared to conventional only simple HT with DCs. These phenomena also occurred in non-treated contralateral tumors as well as treated ones. Our data suggest that the combination of 43 °C preheated simple HT SCCVII tumors and additional 41 °C heat mHT promotes DC maturation, resulting in suppression of tumor growth systemically and lifetime prolongation in mice. 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subjects | Animals Biological and medical sciences Blotting, Western Carcinoma, Squamous Cell - therapy Dendritic Cells - transplantation Dermatology Female Fluorescent Antibody Technique HSP70 Heat-Shock Proteins - biosynthesis Hyperthermia, Induced Immunotherapy - methods Medical sciences Mice Mice, Inbred C3H Tumors Tumors of the skin and soft tissue. Premalignant lesions |
title | Optimization of hyperthermia and dendritic cell immunotherapy for squamous cell carcinoma |
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