Copper enhances genotoxic drug resistance via ATOX1 activated DNA damage repair

Jing Jin, Mingjun Ma, Shaohui Shi, Jiaru Wang, Pengyu Xiao, Hai Fan Yu, Chao Zhang, Qiang Guo, Ze Yu, Zhenkun Lou, Chun Bo Teng

Research output: Contribution to journalArticlepeer-review


Copper is involved in various biochemical and physiological processes. The absorbed copper ions are transported to the intracellular destination via copper chaperones, such as ATOX1. Previous studies have demonstrated that neoplastic cells have a high demand for copper; however, its role in cancer cells has not been fully elucidated. Here, we reveal that the high level of copper contributes to drug resistance and repair of damaged DNA in cancer cells at least partially via ATOX1-induced expression of MDC1, a crucial protein involved in double-strand DNA damage repair. Specifically, ATOX1 enters into nuclear to target MDC1 promoter after treatments of various genotoxic agents, thus promoting the transcription of MDC1 in a copper-dependent manner. Therefore, knockout or blockage of ATOX1 conferred sensitivity to Gemcitabine in transplanted tumor mouse models. Together, our findings gain new insight into the role of copper in DNA damage repair and provide a novel strategy for clinical cancer therapy of drug-resistance cancers.

Original languageEnglish (US)
Article number215651
JournalCancer Letters
StatePublished - Jun 28 2022

ASJC Scopus subject areas

  • Oncology
  • Cancer Research


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