Enhanced cytotoxic T cell function and suppression of tumor development by Mst1 deficiency
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- Yasuda Kaneki
- Department of Urology and Andrology, Kansai Medical University
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- Ueda Yoshihiro
- Department of Molecular Genetics, Kansai Medical University
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- Ozawa Madoka
- Department of Molecular Genetics, Kansai Medical University
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- Matsuda Tadashi
- Department of Urology and Andrology, Kansai Medical University
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- Kinashi Tatsuo
- Department of Molecular Genetics, Kansai Medical University
Bibliographic Information
- Other Title
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- Mst1欠損による増強された細胞障害性T細胞の機能と腫瘍発達の抑制
- Mst1 ケッソン ニ ヨル ゾウキョウ サレタ サイボウ ショウガイセイ Tサイボウ ノ キノウ ト シュヨウ ハッタツ ノ ヨクセイ
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Description
<p>Cytotoxic CD8 T lymphocytes are the major cells of the immune response to viral infection and tumor rejection. Differentiated CTLs have a large number of modified lysosomes including perforin and granzyme B.</p><p>Mammalian ste-20 like kinase Mst1 is abundantly expressed on lymphocytes and plays important roles during apoptosis, proliferation, cell polarity, and migration.</p><p>Here, we report the new role of Mst1 for cytotoxic T-cell responses and tumor reduction.</p><p>Mst1–/– cytotoxic T cells also showed enhanced T-bet expression associated with elevated expression levels of IFNγ and granzyme B.</p><p>In addition, Mst1–/– cytotoxic T cells suppressed tumor growth and prolonged overall survival of tumor bearing mice in vivo.</p><p>Thus, Mst1 is a potential therapeutic target for tumor immunotherapy.</p>
Journal
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- The Journal of Kansai Medical University
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The Journal of Kansai Medical University 68 (0), 9-15, 2017
The Medical Society of Kansai Medical University
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Details 詳細情報について
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- CRID
- 1390001204946463360
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- NII Article ID
- 130006218931
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- NII Book ID
- AN00046712
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- ISSN
- 21853851
- 00228400
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- NDL BIB ID
- 028762287
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- Text Lang
- ja
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- Data Source
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- JaLC
- NDL Search
- Crossref
- CiNii Articles
- OpenAIRE
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- Abstract License Flag
- Disallowed