Long Noncoding RNA ANRIL Supports Proliferation of Adult T-Cell Leukemia Cells through Cooperation with EZH2

Author:

Song Zaowen1,Wu Wencai1,Chen Mengyun1,Cheng Wenzhao2,Yu Juntao1,Fang Jinyong1,Xu Lingling13,Yasunaga Jun-ichirou4,Matsuoka Masao45,Zhao Tiejun13

Affiliation:

1. College of Chemistry and Life Sciences, Zhejiang Normal University, Jinhua, Zhejiang, China

2. Biomedical Department, Huaqiao University, Quanzhou, China

3. Key Laboratory of Wildlife Biotechnology and Conservation and Utilization of Zhejiang Province, Zhejiang Normal University, Jinhua, Zhejiang, China

4. Laboratory of Virus Control, Institute for Frontier Life and Medical Sciences, Kyoto University, Kyoto, Japan

5. Department of Hematology, Rheumatology and Infectious Diseases, Kumamoto University School of Medicine, Kumamoto, Japan

Abstract

Human T-cell leukemia virus type 1 (HTLV-1) is the pathogen that causes adult T-cell leukemia (ATL), which is a unique malignancy of CD4 + T cells. A role for long noncoding RNA (lncRNA) in HTLV-1-mediated cellular transformation has not been described. In this study, we demonstrated that the lncRNA ANRIL was important for maintaining the proliferation of ATL cells in vitro and in vivo . ANRIL was shown to activate NF-κB signaling through forming a ternary complex with EZH2 and p65. Furthermore, epigenetic inactivation of p21/CDKN1A was involved in the oncogenic function of ANRIL. To the best of our knowledge, this is the first study to address the regulatory role of the lncRNA ANRIL in ATL and provides an important clue to prevent or treat HTLV-1-associated human diseases.

Funder

National Natural Science Foundation of China

Zhejiang Province Public Welfare Technology Application Research Project

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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