细胞毒性
癌症研究
免疫学
分泌物
癌症
TRPM2型
癌细胞
生物
体外
受体
内分泌学
生物化学
遗传学
瞬时受体电位通道
作者
Maya Gershkovitz,Yaki Caspi,Tanya Fainsod-Levi,Ben Katz,Janna Michaeli,Saleh Khawaled,Shaya Lev,Lola Polyansky,Merav E. Shaul,Ronit Vogt Sionov,Leonor Cohen‐Daniel,Rami I. Aqeilan,Yoav D. Shaul,Yasuo Mori,Rotem Karni,Zvi G. Fridlender,Alexander M. Binshtok,Zvi Granot
出处
期刊:Cancer Research
[American Association for Cancer Research]
日期:2018-05-14
卷期号:78 (10): 2680-2690
被引量:140
标识
DOI:10.1158/0008-5472.can-17-3614
摘要
Neutrophils play a critical role in cancer, with both protumor and antitumor neutrophil subpopulations reported. The antitumor neutrophil subpopulation has the capacity to kill tumor cells and limit metastatic spread, yet not all tumor cells are equally susceptible to neutrophil cytotoxicity. Because cells that evade neutrophils have greater chances of forming metastases, we explored the mechanism neutrophils use to kill tumor cells. Neutrophil cytotoxicity was previously shown to be mediated by secretion of H2O2 We report here that neutrophil cytotoxicity is Ca2+ dependent and is mediated by TRPM2, a ubiquitously expressed H2O2-dependent Ca2+ channel. Perturbing TRPM2 expression limited tumor cell proliferation, leading to attenuated tumor growth. Concomitantly, cells expressing reduced levels of TRPM2 were protected from neutrophil cytotoxicity and seeded more efficiently in the premetastatic lung.Significance: These findings identify the mechanism utilized by neutrophils to kill disseminated tumor cells and to limit metastatic spread. Cancer Res; 78(10); 2680-90. ©2018 AACR.
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