Effects of LncRNA Lnc-LIF-AS on cell proliferation, migration and invasion in a human cervical cancer cell line

被引:6
作者
Song, Weiguo [1 ]
Wang, Juan [1 ]
Liu, Hanyuan [1 ]
Zhu, Chenchen [1 ]
Xu, Fei [1 ]
Qian, Lili [2 ]
Shen, Zhen [2 ]
Zhu, Jing [2 ]
Yin, Shuai [3 ]
Qin, Jiwei [3 ]
Chen, Liang [4 ]
Wu, Dabao [2 ]
Nashan, Bjorn [3 ]
Shan, Ge [4 ]
Xiao, Weihua [4 ]
Zhou, Ying [1 ]
机构
[1] Anhui Med Univ, Anhui Prov Hosp, Dept Obstet & Gynecol, Hefei 230001, Anhui, Peoples R China
[2] Univ Sci & Technol China, Anhui Prov Hosp, Affiliated Hosp 1, Dept Obstet & Gynecol, Hefei 230001, Anhui, Peoples R China
[3] Univ Sci & Technol China, Anhui Prov Hosp, Affiliated Hosp 1, Organ Transplantat Ctr, Hefei 230001, Anhui, Peoples R China
[4] Univ Sci & Technol China, CAS Key Lab Innate Immun & Chron Dis, Hefei Natl Lab Phys Sci Microscale, Sch Life Sci, Hefei 230027, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
LncRNA; Cervical cancer; Proliferation; Migration; Invasion; LONG NONCODING RNAS; STAT3; GENE; INFLAMMATION; METASTASIS; ACTIVATION; INSIGHTS; IL-6;
D O I
10.1016/j.cyto.2019.05.004
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
This study explored the effect of LncRNA Lnc-LIF-AS on cell proliferation, migration and invasion in the human cervical cancer (HCC) cell line SiHa. SiHa cells had the lowest expression of Lnc-LIF-AS in the 4 human cervical cancer cell lines (SiHa, ME-180, C-33A and HeLa) and were transfected and divided into the SiHa/con (transfected with pMIGRI) cell group, SiHa/Lnc-LIF-AS (transfected with pMIGRI-Lnc-LIF-AS) cell group, and SiHa/Lnc-LIF-AS-DN (transfected with pMIGRI-Lnc-LIF-AS-DN, in which the sequences overlapping with LIF mRNA was deleted) cell group. Overexpression of Lnc-LIF-AS could promote the proliferation, colony formation, invasion and migration in SiHa and ME-180 cells. And the low expression of Lnc-LIF-AS suppress the proliferation, colony formation invasion and migration in HeLa cells when the Lnc-LIF-AS expression has been suppressed. In the SiHa/Lnc-LIF-AS cells group, the cell cycle was mainly halted in the S phase and overexpression of Lnc-LIF-AS had no effect on the apoptosis of SiHa cells. Overexpression of Lnc-LIF-AS could promote the secretion of LIF in SiHa cells, and the supernatant from SiHa/Lnc-LIF-AS cells could promote cell proliferation in the SiHa/con cells. The STAT3 inhibitor could inhibit cell proliferation in the SiHa/Lnc-LIF-AS cells. The expression level of Lnc-LIF-AS in cervical cancer tissues was higher than that in normal tissues and the expression level of Lnc-LIF-AS was positively correlated with the level of LIF. In the SiHa/con and SiHa/Lnc-LIF-AS-DN cell groups, there were no significant differences in cell proliferation, cell migration and cell invasion. The overexpression of Lnc-LIF-AS can promote cell proliferation, migration and invasion in cervical cancer cells, and the core function domain of this lncRNA was located in the overlapping a 3'-UTR base sequence of LIF mRNA.
引用
收藏
页码:165 / 175
页数:11
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