Downregulation of circular RNA circ-LDLRAD3 suppresses pancreatic cancer progression through miR-137-3p/PTN axis

被引:59
|
作者
Yao, Jun [1 ,2 ]
Zhang, Ce [1 ,2 ]
Chen, Yanfei [1 ,2 ]
Gao, Shegan [1 ,2 ]
机构
[1] Henan Univ Sci & Technol, Coll Clin Med, Affiliated Hosp 1, Henan Key Lab Canc Epigenet,Canc Inst, Luoyang 471003, Henan, Peoples R China
[2] Henan Univ Sci & Technol, Coll Clin Med, Affiliated Hosp 1, Luoyang 471003, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
Pancreatic cancer; Circular RNA; Circ-LDLRAD3; miR-137-3p; Pleiotrophin; PERINEURAL INVASION; PLEIOTROPHIN; EPIDEMIOLOGY; DIAGNOSIS; SPONGES;
D O I
10.1016/j.lfs.2019.116871
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Emerging evidence suggests that dysregulation of circular RNAs (circRNAs) closely associated with cancer progression. In this paper, we focus on exploring the functional role of circ-LDLRAD3 in pancreatic cancer. Gene expression was determined using quantitative reverse transcriptase polymerase chain reaction and Western blot. Cell count kit-8 and 5-ethynyl-2'-deoxyuridine assay were applied to evaluate the proliferation of PANC-1 and SW1990 cells. The migration and invasion of PANC-1 and SW1990 cells were assessed using wound healing assay and transwell invasion assay. Luciferase reporter assay was performed for target validation. The results showed that circ-LDLRAD3 was overexpressed in pancreatic cancer tissues and cell lines. Increased expression of circ-LDLRAD3 was indicative of a poor prognosis in patients with pancreatic cancer. Knockdown of circ-LDLRAD3 repressed the growth of pancreatic cancer in vitro and in vivo. miR-137-3p was identified as a direct target of circ-LDLRAD3. More importantly, upregulation of circ-LDLRAD3 could mitigate the inhibitory effect of miR-137-3p on the proliferation, migration and invasion of pancreatic cancer cells. Besides, circ-LDLRAD3 could regulate the expression of pleiotrophin (PTN) through miR-137-3p. Taken together, knockdown of circ-LDLRAD3 repressed the proliferation, migration and invasion of pancreatic cancer cells through miR-137-3p/PTN axis, providing a new mechanism for pancreatic cancer progression.
引用
收藏
页数:9
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