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5097955 
Journal Article 
XRCC4, which is inhibited by PFDA, regulates DNA damage repair and cell chemosensitivity 
Liu, F; Fan, Z; Song, N; Han, M; Yan, M; Guo, LH; Jihui, J; Liu, S 
2019 
Yes 
Journal of Cellular Biochemistry
ISSN: 0730-2312
EISSN: 1097-4644 
120 
12665-12676 
English 
The mechanism of environmental pollution promoting gastric cancer incidence and difficulty of treatment is not fully understood. In the present article, perfluorodecanoic acid (PFDA), a common persistent environmental pollutant, was used to treat the gastric cell lines and mice to test its genotoxicity. The γ-H2AX immunoblot and plasmid fragment PCR results showed that PFDA had a promotion effect on the DNA double-strand breaks (DSBs) in human and mouse cells. Subsequent results showed that PFDA significantly altered the sensitivity of cells to chemotherapy. Microarray data showed that the expressions of some important DNA repair genes were changed. Further investigation discovered that PFDA inhibition of DNA repair was mediated by X-ray repair cross complementing 4 (XRCC4). The cells deficient in XRCC4 generally exhibited reduced proliferation and premature aging in culture; however, our results indicated that PFDA induced p53 inhibition rescued cells from the apoptosis that was triggered by nonhomologous end-joining (NHEJ) inactivation, and overexpression of p53 expression in PFDA-treated cells enhanced their apoptosis. Finally, T-cell specific factor 4 was suggested by the results as an upstream regulator of XRCC4. This article revealed for the first time that perfluorinated chemicals affect chemotherapeutic sensitivity and the NHEJ pathway, and p53 reduction rescues cells from death. 
chemotherapeutic sensitivity; DNA double-strand breaks (DSBs); p53; perfluorodecanoic acid (PFDA); X-ray repair cross complementing 4 (XRCC4)