ZNF131-BACH1 transcriptionally accelerates RAD51-dependent homologous recombination repair and therapy-resistance of non-small-lung cancer cells by preventing their degradation from CUL3
Mingwei Fan, Quanbo Liu, Xiaowen Ma, Yufeng Jiang, Yilong Wang, Shuting Jia, Y. Nie, Ruoyi Deng, Pengchong Zhou, Shuyu Zhang, Siyu Jiang, Mengyao Guan, Yuekang Hou, Yuan Miao, Yong Zhang, Xiupeng Zhang
Abstract
Our findings indicate that ZNF131 exhibits heightened expression in NSCLC, driving essential processes such as proliferation, invasion, and stemness by transcriptionally activating RAD51. The ZNF131-BACH1 interaction serves as a crucial enhancer, further boosting RAD51 transcription and ultimately accelerating therapy resistance in NSCLC.
Topics & Concepts
RAD51Homologous recombinationCancer researchHomologous chromosomeDegradation (telecommunications)Lung cancerChemistryCell biologyBiologyMedicinePathologyBiochemistryDNAComputer scienceGeneTelecommunicationsDNA Repair MechanismsPARP inhibition in cancer therapyMolecular Biology Techniques and Applications