MiR-9-1 Suppresses Cell Proliferation and Promotes Apoptosis by Targeting UHRF1 in Lung Cancer

Author:

Jia Cheng-You1,Xiang Wei2,Liu Ji-Bin3,Jiang Geng-Xi4,Sun Feng3,Wu Jian-Jun5,Yang Xiao-Li1,Xin Rui1,Shi Yi1,Zhang Dan-Dan1,Li Wen6,Zuberi Zavuga7,Zhang Jie8,Lu Gai-Xia1,Wang Hui-Min1,Wang Pei-Yao1,Yu Fei1,Lv Zhong-Wei1,Ma Yu-Shui19,Fu Da1ORCID

Affiliation:

1. Shanghai Tenth People’s Hospital, Tongji University School of Medicine, Shanghai, China

2. Shanghai Punan Hospital, Shanghai, China

3. Cancer Institute, Affiliated Tumor Hospital of Nantong University, Nantong, China

4. Navy Military Medical University Affiliated Changhai Hospital, Shanghai, China

5. Nantong Haimen Yuelai Health Centre, Haimen, China

6. Central South University of Forestry and Technology, Changsha, Hunan, China

7. Dares Salaam Institute of Technology, Salaam, Tanzania

8. School of Medicine, Nantong University, Nantong, China

9. Eastern Hepatobiliary Surgery Hospital/Institute, National Center for Liver Cancer, the Second Military Medical University, Shanghai, China

Abstract

Lung cancer is listed as the most common reason for cancer-related death all over the world despite diagnostic improvements and the development of chemotherapy and targeted therapies. MicroRNAs control both physiological and pathological processes including development and cancer. A microRNA-9 to 1 (miR-9 to 1) overexpression model in lung cancer cell lines was established and miR-9 to 1 was found to significantly suppress the proliferation rate in lung cancer cell lines, colony formation in vitro, and tumorigenicity in nude mice of A549 cells. Ubiquitin-like containing PHD and RING finger domains 1 (UHRF1) was then identified to direct target of miR-9 to 1. The inhibition of UHRF1 by miR-9 to 1 causes G1 arrest and p15, p16, and p21 were re-expressed in miR-9 to 1 group in mRNA level and protein level. Silence of UHRF1 expression in A549 cells resulted in the similar re-expression of p15, p16, p21 which is similar with miR-9 to 1 infection. Therefore, we concluded that UHRF1 is a new target for miR-9 to 1 to suppress cell proliferation by re-expression of tumor suppressors p15, p16, and p21 mediated by UHRF1.

Funder

National Natural Science Foundation of China

Publisher

SAGE Publications

Subject

Cancer Research,Oncology

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