Young CheunMyong Chul KoagYoussef W. NaguibHala Ouzon-ShubeitaZhengrong CuiDanaya PakotipraphaSeongmin LeeUniversity of Texas at AustinMahidol UniversityMinia University2019-08-232019-08-232018-01-01Chemical Biology and Drug Design. Vol.91, No.1 (2018), 116-12517470285174702772-s2.0-85026459977https://repository.li.mahidol.ac.th/handle/20.500.14594/45312© 2017 John Wiley & Sons A/S. Cisplatin resistance is caused, in part, by the efficient removal of the helix-distorting cisplatin 1,2-intrastrand cross-links by nucleotide excision repair (NER) machinery. To make a platinum-DNA adduct that causes less helical distortion than the cisplatin 1,2-intrastrand adduct, we designed and synthesized a monofunctional platinum-carbazole conjugate (carbazoplatin). The 2.5 Å crystal structure of carbazoplatin-DNA adduct revealed both the monoplatination of the N7 of a guanine (G) base and the intercalation into two G:C base pairs, while causing a minor distortion of the DNA helix. A 50-mer dsDNA containing a single carbazoplatin lesion was poorly processed by UvrABC endonuclease, the prokaryotic NER machinery that detects helical distortion and performs dual incision around the lesion. Our cell viability assay indicated that the cytotoxic pathways of carbazoplatin might be different from those of cisplatin; carbazoplatin was 5–8 times more cytotoxic than cisplatin against PANC-1 and MDA-MB-231 cancer cell lines.Mahidol UniversityBiochemistry, Genetics and Molecular BiologyChemistryPharmacology, Toxicology and PharmaceuticsArticleSCOPUS10.1111/cbdd.13062