Long non-coding RNA DSCAM-AS1 contributes to the tumorigenesis of cervical cancer by targeting miR-877-5p/ATXN7L3 axis

被引:40
|
作者
Liang, Jie [1 ]
Zhang, Shujuan [2 ]
Wang, Wei [3 ]
Xu, Yan [1 ]
Kawuli, Atikan [2 ]
Lu, Jiaqi [1 ]
Xiu, Xuemei [2 ]
机构
[1] Second Peoples Hosp Kashgar, Dept Gynaecol, 1 Hlth Rd, Kashgar 844000, Xinjiang, Peoples R China
[2] Second Peoples Hosp Kashgar, Dept Med Oncol, 1 Hlth Rd, Kashgar 844000, Xinjiang, Peoples R China
[3] First Peoples Hosp Kashgar, Dept Med Oncol, 120 Yingbin Rd, Kashgar 844000, Xinjiang, Peoples R China
关键词
CELL-PROLIFERATION; POOR-PROGNOSIS; EXPRESSION; MIGRATION; INVASION; GROWTH; CERNA;
D O I
10.1042/BSR20192061
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cervical cancer (CC) is ranked as the fourth most common cancer that occurs in women universally, which normally causes pain in the lower belly. Plenty of studies have stated that the expression of long non-coding RNAs (lncRNAs) is linked to the cellular development of many kinds of cancers. DSCAM-AS1 has been reported to act as an oncogene in other cancer types and the aim of our study was to uncover the function and regulatory mechanism of DSCAM-AS1 in CC. In this research, our findings presented that DSCAM-AS1 expression was up-regulated in CC cells. DSCAM-AS1 led to the development of CC by enhancing cell proliferation, migration and invasion ability. DSCAM-AS1 was verified to combine with miR-877-5p and down-regulate the expression of miR-877-5p. Results also showed that ATXN7L3 was a downstream target gene of miR-877-5p and it was unfavorably modulated by miR-877-5p. Enhanced expression of ATXN7L3 counterbalanced the DSCAM-AS1 knockdown effect on the progression of CC. This was the first time to analyze the underlying regulatory mechanism of the oncogenic DSCAM-AS1. Our findings clarified that DSCAM-AS1 played as an oncogenic lncRNA by targeting miR-877-5p/ATXN7L3 axis to promote CC progression, which may provide insights into the prevention of CC.
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页数:10
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