Literature DB >> 27912060

The Hippo Pathway Kinases LATS1/2 Suppress Cancer Immunity.

Toshiro Moroishi1, Tomoko Hayashi2, Wei-Wei Pan3, Yu Fujita4, Matthew V Holt5, Jun Qin5, Dennis A Carson2, Kun-Liang Guan6.   

Abstract

Poorly immunogenic tumor cells evade host immunity and grow even in the presence of an intact immune system, but the complex mechanisms regulating tumor immunogenicity have not been elucidated. Here, we discovered an unexpected role of the Hippo pathway in suppressing anti-tumor immunity. We demonstrate that, in three different murine syngeneic tumor models (B16, SCC7, and 4T1), loss of the Hippo pathway kinases LATS1/2 (large tumor suppressor 1 and 2) in tumor cells inhibits tumor growth. Tumor regression by LATS1/2 deletion requires adaptive immune responses, and LATS1/2 deficiency enhances tumor vaccine efficacy. Mechanistically, LATS1/2-null tumor cells secrete nucleic-acid-rich extracellular vesicles, which induce a type I interferon response via the Toll-like receptors-MYD88/TRIF pathway. LATS1/2 deletion in tumors thus improves tumor immunogenicity, leading to tumor destruction by enhancing anti-tumor immune responses. Our observations uncover a key role of the Hippo pathway in modulating tumor immunogenicity and demonstrate a proof of concept for targeting LATS1/2 in cancer immunotherapy. Copyright Â
© 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  B16 melanoma; Hippo; LATS; TAZ; Toll-like receptor; YAP; cancer immunity; exosome; immunotherapy; interferon

Mesh:

Substances:

Year:  2016        PMID: 27912060      PMCID: PMC5512418          DOI: 10.1016/j.cell.2016.11.005

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  41 in total

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  149 in total

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