LncRNA MALAT1 promotes proliferation and metastasis of cervical cancer cell via regulating miR-124-3p/IGF2BP1 axis
10.3872/j.issn.1007-385x.2019.02.007
- VernacularTitle:LncRNA MALAT1通过调控miR-124-3p/IGF2BP1分子轴促进宫颈癌 细胞增殖和转移
- Author:
ZHOU Li
1
;
QIN Juan
1
;
LU Anwei
1
Author Information
1. (Department of Obstetrics and Gynecology, Maternal and Child Health Hospital of Guiyang City
- Publication Type:Journal Article
- Keywords:
cervical cancer;
proliferation;
epithelial mesenchymal transition;
lncRNAMALAT1；miR-124-3p;
IGF2BP1
- From:
Chinese Journal of Cancer Biotherapy
2019;26(2):182-189
- CountryChina
- Language:Chinese
-
Abstract:
Objective: To investigate the mechanism of lncRNA MALAT1 modulating proliferation and metastasis of cervical cancer cells via regulating miR-124-3p/IGF2BP1 axis. Methods: A total of 45 cases of cervical cancer tissues and corresponding paracancerous tissues resected from patients, who were admitted to the Department of Obstetrics and Gynecology of Guiyang Maternal and Child Health Hospital during April 2014 and December 2017, were included in this study; in addition, cervical cancer cell lines SiHa, Caski, HeLa and C33awere also collected for this study. qPCR was applied to detect the expression of MALAT1 in cervical cancer tissues and cell lines. MALAT1-knockdown vectors, miR-124-3p inhibitors and IGF2BP1-overexpression vectors were constructed and used to transfect cervical cancer cells, respectively; the influence of MALAT1 or MALAT1 knockdown on cell proliferation, invasion and epithelial mesenchymal transition (EMT) via miR-124-3p/IGF2BP1 axis were determined by CCK-8 assay, Transwell assay, Wb and immunofluorescence, respectively. The interaction between MALAT1, miR-124-3p, and IGF2BP1 were verified by dual luciferase reporter gene assay. Results: MALAT1 was up-regulated in cervical cancer tissues and cell lines (P<0.05 or P<0.01). Meanwhile, MALAT1 knockdown remarkably inhibited proliferation, invasion and EMT of cervical cancer cells (P<0.05 or P<0.01). Moreover, dual-luciferase reporter gene assay showed that MALAT1 directly interacted with miR-124-3p and down-regulated its expression, while miR-1243p negatively regulated IGF2BP1 expression. Our experiment further validated that MALAT1 knockdown suppressed proliferative, invasion and EMT of cervical cancer cells via inducing the inhibitory effect of miR-124-3p on IGF2BP1 (P<0.05 or P<0.01). Conclusion: MALAT1 promotes the proliferation, invasion and EMT of cervical cancer cells by down-regulating miR-124-3p/IGF2BP1 axis, which provides potential molecular targets for early diagnosis or treatment of cervical cancer.
- Full text:20190207.pdf
