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TGF-beta and tumors - an ill-fated alliance

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CURRENT OPINION IN IMMUNOLOGY
卷 20, 期 2, 页码 234-240

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CURRENT BIOLOGY LTD
DOI: 10.1016/j.coi.2008.04.003

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资金

  1. Intramural NIH HHS [Z01 DE000046-37] Funding Source: Medline
  2. NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH [ZIADE000046] Funding Source: NIH RePORTER

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Mechanisms of host defense can form an unwitting alliance with tumor cells to promote tumor progression, invasion, and dissemination to distant sites. By secreting TGF-beta, an immunoregulatory molecule designated for both promoting inflammation and dampening immune responses, the tumor tricks the host into supporting its expansion and survival. TGF-beta not only recruits leukocytes to secrete chemokines, growth factors, cytokines, and proteases in support of a tumor-friendly niche but also in a context-specific manner, incapacitates the emergent immune response. As a profound immunosuppressant, TGF-beta, both directly and through the generation of regulatory T cells, blunts immune surveillance, favoring tumor escape. Collectively, the ability of the tumor to hijack these host defense pathways can tip the balance in favor of the tumor.

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