Basic & Clinical Medicine ›› 2025, Vol. 45 ›› Issue (8): 1073-1077.doi: 10.16352/j.issn.1001-6325.2025.08.1073

• Original Articles • Previous Articles     Next Articles

Knockdown of translocase of inner mitochondrial membrane 8A enhances gefitinib sensitivity to lung cancer cell line PC-9

CHEN Lei*,REN Weihao,WANG Lide   

  1. Department of Thoracic Surgery, Peking University Shougang Hospital, Beijing 100144, China
  • Received:2025-04-30 Revised:2025-06-10 Online:2025-08-05 Published:2025-07-11
  • Contact: *chenlei_sghospital@163.com

Abstract: Objective To explore the alteration and function of TIMM8A during gefitinib-induced growth inhibition of lung cancer cell line PC-9. Methods TIMM8A siRNA transfection experiment was used to inhibit the expression of TIMM8A in PC-9 and gefitinib resistant PC-9 cells (PC-9-MTAC). CCK-8 assay was carried out to assess PC-9 and PC-9-MTAC cell viability after gefitinib treatment or TIMM8A siRNA transfection. qPCR was used to determine TIMM8A expression in PC-9 or PC-9-MTAC cells. Results Gefitinib inhibited PC-9 cell growth in a dose-dependent manner. The expression of TIMM8A was inhibited during this process, and more than 50% TIMM8A expression had been inhibited by 25 nmol/L gefitinib, while knockdown of TIMM8A enhanced inhibitory effects of gefitinib on PC-9 cell proliferation(P<0.05). Compared with the sensitive cells, treatment of the gefitinib-resistant PC-9-MTAC with 100 nmol/L gefitinib for 48 h only inhibited approximately 30% of TIMM8A expression. Furthermore, inhibition of TIMM8A expression enhanced the sensitivity of PC-9-MTAC cells to gefitinib(P<0.05). Conclusions Low expression of TIMM8A improves anti-tumor effects of gefitinib in lung cancer cell line PC-9.

Key words: lung cancer, targeted therapy, gefitinib, drug resistance, TIMM8A

CLC Number: