LOXL1-AS1 promotes cell proliferation in hepatocellular carcinoma through miR-1224-5p/ITPRIPL2/AKT axis

被引:3
|
作者
Chen, Tangen [1 ]
Zeng, Shuyun [2 ]
Liu, Quanyuan [1 ]
Chen, Yufeng [1 ]
Lu, Junjiang [1 ]
机构
[1] Zhangzhou Municipal Hosp Fujian Prov, Dept Hepatobiliary Surg, Zhangzhou 363000, Fujian, Peoples R China
[2] Zhangzhou Municipal Hosp Fujian Prov, Dept Cardiovasc Med, Dept Neurosurg, Zhangzhou 363000, Fujian, Peoples R China
关键词
AKT pathway; ITPRIPL2; LOXL1-AS1; miR-1224-5p; Primary hepatocellular carcinoma; LONG NONCODING RNA; GASTRIC-CANCER; TUMOR-SUPPRESSOR; MIR-1224-5P; EXPRESSION; APOPTOSIS; INVASION; ACTS;
D O I
10.14715/cmb/2023.69.7.8
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
LncRNA has been validated to be related to different cancers, whereas its regulation mechanism in hepatocellular carcinoma (HCC) is poorly known. In this study, LOXL1-AS1 was overexpressed in HCC cell lines, and LOXL1-AS1 knockdown repressed cell proliferation and stimulated apoptosis in HCC. Besides, the activating role of LOXL1-AS1 in the AKT pathway was also confirmed. Further, miR-1224-5p was sponged by LOXL1-AS1, and overexpression exerted inhibitory function in HCC. Moreover, ITPRIPL2 as amiR-1224-5ptarget gene. Meanwhile, ITPRIPL2 deficiency suppressed HCC cell proliferation. Finally, miR-1224-5p inhibitor reversed the hindering role of LOXL1-AS1 depletion in HCC cell proliferation and AKT pathway, and this rescuing effect was offset by ITPRIPL2 silencing. In summary, LOXL1-AS1 induced cell proliferation and suppresses cell apoptosis in primary HCCvia activating AKT pathway, sponging miR-1224-5p and upregulating ITPRIPL2, which may provide some fresh thoughts for researches about the molecular regulation mechanism of lncRNA in HCC.
引用
收藏
页码:45 / 50
页数:6
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