ARID1A Inactivation Increases Expression of circ0008399 and Promotes Cisplatin Resistance in Bladder Cancer

• Published in: Current medical science 2023-06, Vol.43 (3), p.560-571
• Main Authors: Jiang, Yang-kai, Shuai, Yu-jun, Ding, Hua-min, Zhang, Hui, Huang, Chao, Wang, Liang, Sun, Jia-yin, Wei, Wen-jie, Xiao, Xing-yuan, Jiang, Guo-song
• Format: Article
• Language: English
• Subjects: Cell Line, Tumor; Cisplatin - pharmacology; Cisplatin - therapeutic use; DEAD-box RNA Helicases - genetics; DEAD-box RNA Helicases - metabolism; DEAD-box RNA Helicases - pharmacology; DNA-Binding Proteins - genetics; DNA-Binding Proteins - metabolism; Drug Resistance, Neoplasm - genetics; Epigenesis, Genetic; Eukaryotic Initiation Factor-4A - genetics; Eukaryotic Initiation Factor-4A - metabolism; Eukaryotic Initiation Factor-4A - pharmacology; Humans; Medicine; Medicine & Public Health; Transcription Factors - genetics; Transcription Factors - metabolism; Transcription Factors - pharmacology; Urinary Bladder Neoplasms - drug therapy; Urinary Bladder Neoplasms - genetics
• ISSN: 2096-5230; 2523-899X
• DOI: 10.1007/s11596-023-2731-8

Objective Cisplatin (CDDP)-based chemotherapy is a first-line, drug regimen for muscle-invasive bladder cancer (BC) and metastatic bladder cancer. Clinically, resistance to CDDP restricts the clinical benefit of some bladder cancer patients. AT-rich interaction domain 1A (ARID1A) gene mutation occurs frequently in bladder cancer; however, the role of CDDP sensitivity in BC has not been studied. Methods We established ARID1A knockout BC cell lines using CRISPR/Cas9 technology. IC 50 determination, flow cytometry analysis of apoptosis, and tumor xenograft assays were performed to verify changes in the CDDP sensitivity of BC cells losing ARID1A. qRT-PCR, Western blotting, RNA interference, bioinformatic analysis, and ChIP-qPCR analysis were performed to further explore the potential mechanism of ARID1A inactivation in CDDP sensitivity in BC. Results It was found that ARID1A inactivation was associated with CDDP resistance in BC cells. Mechanically, loss of ARID1A promoted the expression of eukaryotic translation initiation factor 4A3 (EIF4A3) through epigenetic regulation. Increased expression of EIF4A3 promoted the expression of hsa_circ_0008399 (circ0008399), a novel circular RNA (circRNA) identified in our previous study, which, to some extent, showed that ARID1A deletion caused CDDP resistance through the inhibitory effect of circ0008399 on the apoptosis of BC cells. Importantly, EIF4A3-IN-2 specifically inhibited the activity of EIF4A3 to reduce circ0008399 production and restored the sensitivity of ARID1A inactivated BC cells to CDDP. Conclusion Our research deepens the understanding of the mechanisms of CDDP resistance in BC and elucidates a potential strategy to improve the efficacy of CDDP in BC patients with ARID1A deletion through combination therapy targeting EIF4A3.