| Literature DB >> 26091714 |
Jie Tian1, Ke Rui2, Xinyi Tang2, Jie Ma2, Yungang Wang2, Xinyu Tian2, Yue Zhang3, Huaxi Xu2, Liwei Lu4, Shengjun Wang5.
Abstract
Myeloid-derived suppressor cells (MDSCs) play a critical role in tumor-associated immunosuppression, thus affecting effective immunotherapies for cancers. However, the molecular mechanisms involved in regulating the differentiation and function of MDSCs remain largely unclear. In this study, we found that inhibition of microRNA (miR)-9 promoted the differentiation of MDSCs with significantly reduced immunosuppressive function whereas overexpression of miR-9 markedly enhanced the function of MDSCs. Notably, knockdown of miR-9 significantly impaired the activity of MDSCs and inhibited the tumor growth of Lewis lung carcinoma in mice. Moreover, miR-9 regulated MDSCs differentiation by targeting the runt-related transcription factor 1, an essential transcription factor in regulating MDSC differentiation and function. Furthermore, the CREB was found to regulate miR-9 expression in MDSCs. Taken together, our findings have identified a critical role of miR-9 in regulating the differentiation and function of MDSCs.Entities:
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Year: 2015 PMID: 26091714 DOI: 10.4049/jimmunol.1500209
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422