Effect of miR-216a-5p on radiosensitivity of liver cancer cells via targeting KLF12
10.3760/cma.j.cn113030-20230427-00098
- VernacularTitle:miR-216a-5p靶向KLF12对肝癌细胞放射敏感性的影响
- Author:
Yi XU
1
;
Yuandong HUANG
Author Information
1. 成都市第五人民医院（成都中医药大学附属第五人民医院/第二临床医学院）肿瘤科/成都市肿瘤防治所，成都 611130
- Keywords:
Liver neoplasms;
Krüppel-like transcription factor 12;
miR-216a-5p;
Radiosensitivity
- From:
Chinese Journal of Radiation Oncology
2024;33(1):56-61
- CountryChina
- Language:Chinese
-
Abstract:
Objective:To evaluate the effect of miR-216a-5p on the radiosensitivity of liver cancer cells via targeting Krüppel-like transcription factors 12 (KLF12).Methods:Real-time reverse transcription PCR (RT-qPCR) was used to detect miR-216a-5p, KLF12 mRNA levels in normal human liver cells L-02 cells, and human hepatoma cells Huh7, HepG2, Hep3B and MHCC-97H cell lines. HepG2 cells were divided into 0, 2, 4, 6 and 8 Gy irradiation groups, and miR-216a-5p, KLF12 mRNA levels were compared among different groups. HepG2 cells overexpressing miR-216a-5p and / or KLF12 were constructed by plasmid transfection and divided into the miR-NC group (control group), miR-216a-5p group, miR-216a-5p+NC group, miR-216a-5p+KLF12 group, IR+miR-NC group, IR+miR-216a-5p group, IR+miR-216a-5p+NC group, IR+miR-216a-5p+KLF12 group, respectively. miR-216a-5p, KLF12 mRNA levels were compared among different groups. Clone formation assay was used to detect cell radiosensitivity. CCK-8 assay was employed to detect cell proliferation ability. Flow cytometry was adopted to detect cell apoptosis. Single factor ANOVA was used for inter group comparisons. LSD- t test was used for pairwise comparison. Results:Compared with L-02 cells, KLF12 mRNA levels were up-regulated, whereas miR-216a-5p levels were down-regulated in liver cancer cell lines (all P<0.05). Compared with 0 Gy group, KLF12 mRNA levels were down-regulated, whereas miR-216a-5p levels were up-regulated in 2, 4, 6, and 8 Gy groups (all P<0.05). Overexpression of miR-216a-5p or radiation therapy alone could enhance cell radiosensitivity and apoptosis levels, and reduce cell proliferation ability (all P<0.05). Simultaneous radiation treatment with overexpression of miR-216a-5p exerted more significant effects on cells (all P<0.05). Overexpression of KLF12 could partially reverse the aforementioned effects of overexpression of miR-216a-5p ( P<0.05). Conclusion:MiR-216a-5p reduces cell proliferation ability, enhances cell radiosensitivity and apoptosis via regulating KLF12.
