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MiR‐21 controls in situ expansion of CCR6 + regulatory T cells through PTEN/AKT pathway in breast cancer
Author(s) -
Hu Yan,
Wang Chunhong,
Li Yongju,
Zhao Juanjuan,
Chen Chao,
Zhou Ya,
Tao Yijin,
Guo Mengmeng,
Qin Nalin,
Ren Tao,
Wen Zhenke,
Xu Lin
Publication year - 2015
Publication title -
immunology and cell biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.999
H-Index - 104
eISSN - 1440-1711
pISSN - 0818-9641
DOI - 10.1038/icb.2015.37
Subject(s) - pten , tensin , gene silencing , cancer research , protein kinase b , pi3k/akt/mtor pathway , microrna , foxp3 , biology , cancer , breast cancer , signal transduction , immunology , microbiology and biotechnology , immune system , biochemistry , genetics , gene
Our recent evidence showed that prior expansion of CCR6 + Foxp3 + regulatory T cells (Tregs) was important for their dominant enrichment in tumor tissue, which was closely related to poor prognosis of breast cancer patients. However, the underlying regulation mechanism of expansion of CCR6 + Tregs in situ remains largely unknown. In this study, we reported that miR‐21 was highly expressed in CCR6 + Tregs in tumor tissues from a murine breast cancer model. And silencing of miR‐21 could significantly reduce the proliferation of CCR6 + Tregs in vitro . Adoptive cell‐transfer assay further showed that silencing of miR‐21 could alter the enrichment of CCR6 + Tregs in the tumor mass and endow effectively antitumor effect of CD8 + T cells using a murine breast cancer model. Mechanistic evidence showed that silencing of miR‐21 enhanced the expression of its target phosphatase and tensin homolog deleted on chromosome ten (PTEN) and subsequently altered the activation of Akt pathway, which was ultimately responsible for reduced proliferation activity of CCR6 + Tregs. Finally, we further revealed that miR‐21 was also highly expressed on CCR6 + Tregs in clinical breast cancer patients. Therefore, miR‐21 can act as a fine tuner in the regulation of PTEN/Akt pathway transduction in the expansion of CCR6 + Tregs in tumor sites and provided a novel insight into the development of therapeutic strategies for promoting T‐cell immunity by regulating distinct subset of Tregs through targeting specific miRNAs.