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Membrane-bound form of monocyte chemoattractant protein-1 enhances antitumor effects of suicide gene therapy in a model of hepatocellular carcinoma

フォーマット:
論文
責任表示:
Marukawa, Yohei ; Nakamoto, Yasunari ; Kakinoki, Kaheita ; Tsuchiyama, Tomoya ; Iida, Noriho ; Kagaya, Takashi ; Sakai, Yoshio ; Naito, Makoto ; Mukaida, Naofumi ; Kaneko, Shuichi
言語:
英語
出版情報:
Nature Publishing Group, 2012-05-01
著者名:
Marukawa, Yohei
Nakamoto, Yasunari
Kakinoki, Kaheita
Tsuchiyama, Tomoya
Iida, Noriho
Kagaya, Takashi
Sakai, Yoshio
Naito, Makoto
Mukaida, Naofumi
Kaneko, Shuichi
続きを見る
掲載情報:
Cancer Gene Therapy
ISSN:
0929-1903  CiNii Research  Webcat Plus  JAIRO
巻:
19
通号:
5
開始ページ:
312
終了ページ:
319
バージョン:
author
概要:
Suicide gene therapy using the herpes simplex virus thymidine kinase/ganciclovir (HSV-tk/GCV) system combined with monocyte chemoattractant protein-1 (MCP-1) provides significant antitumor efficacy. The current study was designed to evaluate the antitumor immunity of a newly developed membrane-bound form of MCP-1 (mMCP-1) in an immunocompetent mouse model of hepatocellular carcinoma (HCC). A recombinant adenovirus vector (rAd) harboring the human MCP-1 gene and the membrane-spanning domain of the CX3CL1 gene was used. Large amounts of MCP-1 protein were expressed and accumulated on the tumor cell surface. The growth of subcutaneous tumors was markedly suppressed when tumors were treated with mMCP-1, as compared with soluble MCP-1, in combination with the HSV-tk/GCV system (P<0.01). The numbers of Mac-1-, CD4-and CD8a-positive cells were significantly higher in tumor tissues (P<0.05), and tumor necrosis factor (TNF) mRNA expression levels with mMCP-1 were almost five-fold higher than those with soluble MCP-1. These results indicate that the delivery of the mMCP-1 gene greatly enhanced antitumor effects following the apoptotic stimuli by promoting the recruitment and activation of macrophages and T lymphocytes, suggesting a novel strategy of immune-based gene therapy in the treatment of patients with HCC. © 2012 Macmillan Publishers Limited All rights reserved. 続きを見る
URL:
http://hdl.handle.net/2297/31396
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Marukawa, Yohei, Nakamoto, Yasunari, Kakinoki, Kaheita, Tsuchiyama, Tomoya, Iida, Noriho, Kagaya, Takashi, Sakai, &hellip;

Nature Publishing Group

Iida, Noriho, Nakamoto, Yasunari, Baba, Tomohisa, Kakinoki, Kaheita, Li, Ying-Yi, Wu, Yu, Matsushita, Kouji, Kaneko, &hellip;

Oxford University Press

Tsuchiyama, Tomoya, Nakamoto, Yasunari, Sakai, Yoshio, Mukaida, Naofumi, Kaneko, Shuichi

Japanese Cancer Association / Blackwell Publishing Ltd

Takata, Yoshiko, Nakamoto, Yasunari, Nakada, Akiko, Terashima, Takeshi, Arihara, Fumitaka, Kitahara, Masaaki, Kakinoki, &hellip;

Elsevier

Kakinoki, Kaheita, Nakamoto, Yasunari, Kagaya, Takashi, Tsuchiyama, Tomoya, Sakai, Yoshio, Nakahama, Tohru, Mukaida, &hellip;

Wiley-Blackwell

Sunagozaka, Hajime, Honda, Masao, Yamashita, Taro, Nishino, Ryuhei, Takatori, Hajime, Arai, Kuniaki, Yamashita, Tatsuya, &hellip;

Wiley-Blackwell

Tsuchiyama, T., Nakamoto, Yasunari, Sakai, Y., Mukaida, Naofumi, Sawabu, Norio, Kaneko, Shuichi

金沢大学がん研究所

Nakagawa, Hidetoshi, Mizukoshi, Eishiro, Iida, Noriho, Terashima, Takeshi, Kitahara, Masaaki, Marukawa, Yohei, Kitamura, &hellip;

Springer-Verlag

Nakamoto, Yasunari, Mizukoshi, Eishiro, Kitahara, Masaaki, Arihara, Fumitaka, Sakai, Yoshio, Kakinoki, Kaheita, Fujita, &hellip;

Blackwell Publishing

Iida, Noriho, Nakamoto, Yasunari, Baba, Tomohisa, Nakagawa, Hidetoshi, Mizukoshi, Eishiro, Naito, Makoto, Mukaida, &hellip;

American Association for Cancer Research

Terashima, Takeshi, Yamashita, Tatsuya, Arai, Kuniaki, Kawaguchi, Kazunori, Kitamura, Kazuya, Yamashita, Taro, Sakai, &hellip;

Japanese Cancer Association / Blackwell Publishing Ltd