A novel mechanism by which c-MYC is aberrantly activated by epigenetic silencing in cancer cells

Author:

Hu Xuming1,wei ye1,Zhang Meiying2,Dou Chunfeng1,Wang Liping1,Zaib Gul1,Wu Huixian1,Guo Wang1,Wang Xiaoyuan3,Chen Shihao1,Xu Qi1,Guo Mingzhou2,Cui Hengmi1

Affiliation:

1. Yangzhou University

2. Chinese PLA General Hospital

3. The Second Affiliated Hospital of Nanjing Medical University

Abstract

Abstract

Proto-oncogenes are abnormally activated in nearly all types of tumors. However, the epigenetic mechanism of proto-oncogene activation has not yet been well elucidated. Here, we show that a subset of proto-oncogenes, including c-MYC, possess antisense RNAs. Upregulation of c-MYC in cancer tissues was attributed to the silencing of its antisense RNA MYC-AS1 via DNA hypermethylation. MYC-AS1 RNA markedly inhibited the proliferation of cancer cells in vitro and impeded tumor growth in nude mice in vivo by repressing the expression of c-MYC via an RNAi mechanism. MYC-AS1 RNA bound directly to the HuR protein in the cytoplasm, enhancing the RNA stability of MYC-AS1. Furthermore, MYC-AS1 inhibited c-MYC-targeted gene LDHA expression. Our work provides a novel mechanism by which c-MYC is activated in cancer cells by epigenetic silencing of its antisense RNA, which functions as a tumor suppressor.

Publisher

Springer Science and Business Media LLC

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