Abstract |
Inflammation has a central role in cancer progression. Metastatic tumors arise at sites of chronic inflammation, and tumors or tumor-infiltrating immune cells produce inflammatory mediators. By contrast, natural killer (NK) cells and cytotoxic T cells (CTLs) help eliminate premalignant lesions and limit the rate of tumor metastasis. Interleukin (IL)-27 is an IL-12 family cytokine chiefly produced by antigen-presenting cells (APCs) such as dendritic cells (DCs) and macrophages, and alone or in combination with other cytokines, IL-27 boosts antitumor immunity by contributing to the development of NK cells and CTLs - a central immnunomodulatory effect - and by exerting potent antiangiogenic and antimetastatic activities, a local antitumor effect. In this review, we argue that by virtue of its rate-limiting functions in innate and adaptive immune responses, modulating IL-27 holds considerable promise for future cancer immunotherapy.
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Authors | Gopal Murugaiyan, Bhaskar Saha |
Journal | Trends in molecular medicine
(Trends Mol Med)
Vol. 19
Issue 2
Pg. 108-16
(Feb 2013)
ISSN: 1471-499X [Electronic] England |
PMID | 23306374
(Publication Type: Journal Article, Review)
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Copyright | Copyright © 2012 Elsevier Ltd. All rights reserved. |
Chemical References |
- Interleukin-17
- Receptors, Interleukin
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Topics |
- Adaptive Immunity
- Animals
- Humans
- Immunity, Innate
- Immunosuppression Therapy
- Immunotherapy
- Inflammation
(immunology)
- Interleukin-17
(immunology, metabolism)
- Neoplasms
(immunology, pathology, therapy)
- Neovascularization, Pathologic
(immunology, metabolism)
- Receptors, Interleukin
(immunology, metabolism)
- T-Lymphocytes, Regulatory
(immunology)
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