Journal of International Obstetrics and Gynecology ›› 2026, Vol. 53 ›› Issue (4): 390-396.doi: 10.12280/gjfckx.20260116

• Research on Gynecological Malignancies:Original Article • Previous Articles     Next Articles

Mechanism of miR-125b Reversing Cisplatin Resistance in Cervical Cancer SiHa Cells by Targeting BCL-2

WANG Shu-jun, JING Li()   

  1. Department of Gynecology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou 221000, Jiangsu Province, China
  • Received:2026-02-06 Published:2026-08-15 Online:2026-08-25
  • Contact: JING Li E-mail:Ji771821@163.com

Abstract:

Objective: To investigate whether miR-125b affects cisplatin (DDP) resistance in cervical cancer SiHa cells by targeting the regulating the expression of B-cell lymphoma-2 (BCL-2) and to explore its underlying mechanism. Methods: Using human cervical cancer cells (SiHa) and their DDP-resistant cell line SiHa/DDP as subjects, the following groups were established: SiHa group (SiHa cells transfected with mimic-NC), SiHa/DDP group (SiHa/DDP cells transfected with mimic-NC), SiHa+mimic-miR-125b group (SiHa cells transfected with miR-125b mimic), and SiHa/DDP+mimic-miR-125b group (SiHa/DDP cells transfected with miR-125b mimic). The expression of miR-125b was detected by real time fluorescent quantitative polymerase chain reaction (RT-qPCR). Cell viability was assessed using the CCK-8 assay, and the half maximal inhibitory concentration (IC50) of DDP was calculated. Apoptosis was measured by flow cytometry, and the expression of BCL-2 protein was evaluated by Western blotting. The targeting relationship between miR-125b and BCL-2 was validated using a dual-luciferase reporter assay. Results: Compared with the parental SiHa group, the resistant SiHa/DDP group exhibited reduced miR-125b expression and apoptosis rate, along with increased BCL-2 protein expression (all P<0.05). After transfection with mimic-miR-125b, compared with the resistant SiHa/DDP group, the SiHa/DDP+mimic-miR-125b group showed increased miR-125b expression and apoptosis rate, and decreased BCL-2 protein expression (all P<0.05). However, miR-125b expression and apoptosis rate in the SiHa/DDP+mimic-miR-125b group remained lower than those in the SiHa+mimic-miR-125b group, while BCL-2 protein expression remained higher (all P<0.05). The IC50 values of DDP were 7.21 μg/mL and 34.75 μg/mL for the SiHa group and SiHa/DDP group, respectively. The IC50 values for the SiHa+mimic-miR-125b and SiHa/DDP+mimic-miR-125b groups were 5.13 μg/mL and 12.26 μg/mL, respectively. The dual-luciferase reporter assay showed that miR-125b mimic specifically reduced the luciferase activity of the wild-type BCL-2 reporter gene (P<0.05), while it had no effect on the mutant type (P>0.05). Conclusions: miR-125b can reverse DDP resistance in cervical cancer SiHa cells by targeting and inhibiting BCL-2 expression, thereby promoting apoptosis.

Key words: Uterine cervical neoplasms, Carcinoma, MicroRNAs, Cisplatin, Drug resistance, neoplasm, Cell proliferation, Apoptosis, MicroRNA-125b, B-cell lymphoma-2