Nasir Jalal, Jing Wei, Yaxin Jiang, J. Pathak, A. R. Surendranath, Chang Y. Chung
{"title":"低剂量双酚A (BPA)诱导MCF-10A细胞的DNA损伤和致瘤事件","authors":"Nasir Jalal, Jing Wei, Yaxin Jiang, J. Pathak, A. R. Surendranath, Chang Y. Chung","doi":"10.1080/2331205X.2019.1616356","DOIUrl":null,"url":null,"abstract":"Abstract The carcinogenic capacity of Bisphenol A (BPA) at nano-molar concentrations of 8.73 and 17.47 nM (in culture) was evaluated on both normal breast epithelial cells (MCF-10A) and breast cancer cells (MCF-7). The highest DNA damage was recorded at 6 h and MCF-10A cells showed significant increase of IGF1R protein while mRNA expression was unchanged; however, the converse was true for MCF-7 cells. Homology modeling predicted the structure of SPCA1/2 and indicated BPA binding within catalytic domain. Our data indicated that BPA caused detectable DNA damage, inhibited cellular SPCA1/2 protein which eventually dysregulated Ca2+-dependent IGF1R.","PeriodicalId":10470,"journal":{"name":"Cogent Medicine","volume":"28 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Low-dose bisphenol A (BPA)-induced DNA damage and tumorigenic events in MCF-10A cells\",\"authors\":\"Nasir Jalal, Jing Wei, Yaxin Jiang, J. Pathak, A. R. Surendranath, Chang Y. Chung\",\"doi\":\"10.1080/2331205X.2019.1616356\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Abstract The carcinogenic capacity of Bisphenol A (BPA) at nano-molar concentrations of 8.73 and 17.47 nM (in culture) was evaluated on both normal breast epithelial cells (MCF-10A) and breast cancer cells (MCF-7). The highest DNA damage was recorded at 6 h and MCF-10A cells showed significant increase of IGF1R protein while mRNA expression was unchanged; however, the converse was true for MCF-7 cells. Homology modeling predicted the structure of SPCA1/2 and indicated BPA binding within catalytic domain. Our data indicated that BPA caused detectable DNA damage, inhibited cellular SPCA1/2 protein which eventually dysregulated Ca2+-dependent IGF1R.\",\"PeriodicalId\":10470,\"journal\":{\"name\":\"Cogent Medicine\",\"volume\":\"28 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cogent Medicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1080/2331205X.2019.1616356\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cogent Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/2331205X.2019.1616356","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Low-dose bisphenol A (BPA)-induced DNA damage and tumorigenic events in MCF-10A cells
Abstract The carcinogenic capacity of Bisphenol A (BPA) at nano-molar concentrations of 8.73 and 17.47 nM (in culture) was evaluated on both normal breast epithelial cells (MCF-10A) and breast cancer cells (MCF-7). The highest DNA damage was recorded at 6 h and MCF-10A cells showed significant increase of IGF1R protein while mRNA expression was unchanged; however, the converse was true for MCF-7 cells. Homology modeling predicted the structure of SPCA1/2 and indicated BPA binding within catalytic domain. Our data indicated that BPA caused detectable DNA damage, inhibited cellular SPCA1/2 protein which eventually dysregulated Ca2+-dependent IGF1R.