MicroRNA-362 Inhibits Cell Proliferation and Invasion by Directly Targeting SIX1 in Colorectal Cancer
10.3349/ymj.2019.60.5.414
- Author:
Jin'e WAN
1
;
Jian YANG
;
Cuixia QIAO
;
Xiaomei SUN
;
Aiting DI
;
Lize ZHANG
;
Dandan WANG
;
Gang ZHAO
Author Information
1. Department of Hyperbaric Oxygen, The Affiliated Hospital of Qingdao University, Qingdao, China.
- Publication Type:Original Article
- Keywords:
miR-362;
SIX;
proliferation;
invasion;
colorectal cancer
- MeSH:
Cell Line;
Cell Proliferation;
China;
Colorectal Neoplasms;
Down-Regulation;
Humans;
Methods;
MicroRNAs;
Mortality;
Real-Time Polymerase Chain Reaction;
RNA, Messenger
- From:Yonsei Medical Journal
2019;60(5):414-422
- CountryRepublic of Korea
- Language:English
-
Abstract:
PURPOSE: Colorectal cancer (CRC) is the third most common cancer in China and poses high morbidity and mortality. In recent years, increasing evidence has indicated that microRNAs played important functions in the occurrence and development of tumors. The purpose of this study was to identify the biological mechanisms of miR-362 in CRC. MATERIALS AND METHODS: Quantitative real-time PCR was carried out to assess the expression of miR-362 and SIX1. The Kaplan-Meier method was employed to evaluate the 5-year overall survival of CRC patients. The proliferative and invasive abilities of CRC cells were assessed by MTT and transwell assays. RESULTS: miR-362 was significantly decreased in CRC tissues and cell lines, compared to the normal tissues and normal cells. A significant connection was confirmed between the overall survival of 53 CRC patients and low expression of miR-362. Downregulation of miR-362 inhibited the proliferation and invasion through binding to the 3′-UTR of SIX1 mRNA in CRC. Additionally, we discovered that SIX1 was a direct target gene of miR-362 and that the expression of miR-362 had a negative connection with SIX1 expression in CRC. SIX1 could reverse partial functions in the proliferation and invasion in CRC cells. CONCLUSION: miR-362 may be a prognostic marker in CRC and suppress CRC cell proliferation and invasion in part through targeting the 3′-UTR of SIX1 mRNA. The newly identified miR-362/SIX1 axis provides insight into the progression of CRC.
