Casey Hon, S. Nair, P. Smirnov, Hossein Sharifi-Noghabi, Nikta Feizi, Shaun Shepherd, B. Haibe-Kains
{"title":"Consistency of in vitro drug sensitivities within pharmacological classes","authors":"Casey Hon, S. Nair, P. Smirnov, Hossein Sharifi-Noghabi, Nikta Feizi, Shaun Shepherd, B. Haibe-Kains","doi":"10.33137/juls.v15i1.37046","DOIUrl":null,"url":null,"abstract":"Multiple comparative analyses between the common drugs and cell lines of the Genomics of Drug Sensitivity in Cancer (GDSC) and the Cancer Therapeutics Response Portal (CTRP) have previously shown low consistency between the in vitro phenotypic measures of a drug in one study with the other. While several potential sources of inconsistency have been tested, the similar targets of tested compounds has yet to be tested as a contributing factor of discrepancy. This analysis includes two methods of reclassifying drugs into classes based on their targets to identify the truer set of consistent cell lines, showing an increased correlation between the two pharmacogenomic studies.","PeriodicalId":40102,"journal":{"name":"University of Toronto Journal of Undergraduate Life Sciences","volume":" ","pages":""},"PeriodicalIF":0.2000,"publicationDate":"2021-07-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"University of Toronto Journal of Undergraduate Life Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.33137/juls.v15i1.37046","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Multiple comparative analyses between the common drugs and cell lines of the Genomics of Drug Sensitivity in Cancer (GDSC) and the Cancer Therapeutics Response Portal (CTRP) have previously shown low consistency between the in vitro phenotypic measures of a drug in one study with the other. While several potential sources of inconsistency have been tested, the similar targets of tested compounds has yet to be tested as a contributing factor of discrepancy. This analysis includes two methods of reclassifying drugs into classes based on their targets to identify the truer set of consistent cell lines, showing an increased correlation between the two pharmacogenomic studies.