circSLC25A13 acts as a ceRNA to regulate AML progression via miR‐616‐3p/ADCY2 axis

Author:

Wei Wenwen1234,Pan Jiajia1234,Wang Jinghan1234,Mao Shihui1234,Qian Yu1234,Lin Xiangjie1234,Ling Qing1234,Ye Wenle1234,Zhou Yutong1234,Zhao Yanchun1234,Huang Jiansong1234,Huang Xin1234,Ma Zhixin5,Wang Huanping1234,Li Chenying1234,Sun Jie1234,Jin Jie12346ORCID

Affiliation:

1. Department of Hematology, The First Affiliated Hospital Zhejiang University School of Medicine Hangzhou Zhejiang People's Republic of China

2. Zhejiang Provincial Key Laboratory of Hematologic Malignancy Zhejiang University Hangzhou Zhejiang People's Republic of China

3. Zhejiang Provincial Clinical Research Center for Hematological Disorders Hangzhou Zhejiang People's Republic of China

4. Zhejiang University Cancer Center Hangzhou Zhejiang People's Republic of China

5. Department of Laboratorial Medicine, Women's Hospital Zhejiang University School of Medicine Hangzhou Zhejiang People's Republic of China

6. Jinan Microecological Biomedicine Shandong Laboratory Jinan Shandong People's Republic of China

Abstract

AbstractCircular RNAs (circRNAs), a type of endogenous noncoding RNA (ncRNA), exert vital roles in leukemia progression and are promising prognostic factors. Here, we report a novel circRNA, circSLC25A13 (hsa_circ_0081188), which was increased in acute myeloid leukemia (AML) patients with poor overall survival (OS) comparing to patients with good prognosis. Knockdown of circSLC25A13 in AML cells inhibited proliferation and increased cell apoptosis in vitro and in vivo. Enhanced circSLC25A13 expression promoted the survival of AML cells. Mechanistically, circSLC25A13 played as a microRNA sponge of miR‐616‐3p, which inhibited the expression of adenylate cyclase 2 (ADCY2). Downregulation of miR‐616‐3p and overexpression of ADCY2 partially rescued circSLC25A13 deficient induced cell growth arrest. In summary, through competitive absorption of miR‐616‐3p and thereby upregulating ADCY2 expression, circSLC25A13 promoted AML progression. Moreover, circSLC25A13 may represent a potential novel biomarker for the prognosis of AML and offer a potential therapeutic target for AML treatment.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Cancer Research,Molecular Biology

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