{"title":"Understanding AKT-mediated chemoresistance: the relationship between ion channels and AKT activation","authors":"Rédoane Daoudi","doi":"arxiv-2307.07427","DOIUrl":null,"url":null,"abstract":"Overcoming chemoresistance is a challenge for multiple chemotherapeutics\nagents like cisplatin. ABC transporters such as MDR1 or MRPs and PI3K/AKT\npathway have been proposed as actors of chemoresistance in several cancers. In\nthis review we describe two downstream targets of Akt: c-myc and p53 in the\nchemoresistance. We suggest a potential link between p53, c-myc and ABC\ntransporters expression. Consequently a link between Akt and ABC\ntransporters-mediated chemoresistance may exist. Finally we show that Akt\nactivation may be Orai-dependent and/or TRPC-dependent, suggesting that these\nion channels could constitute a therapeutic target in cancer.","PeriodicalId":501170,"journal":{"name":"arXiv - QuanBio - Subcellular Processes","volume":"51 47","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-07-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"arXiv - QuanBio - Subcellular Processes","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/arxiv-2307.07427","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Overcoming chemoresistance is a challenge for multiple chemotherapeutics
agents like cisplatin. ABC transporters such as MDR1 or MRPs and PI3K/AKT
pathway have been proposed as actors of chemoresistance in several cancers. In
this review we describe two downstream targets of Akt: c-myc and p53 in the
chemoresistance. We suggest a potential link between p53, c-myc and ABC
transporters expression. Consequently a link between Akt and ABC
transporters-mediated chemoresistance may exist. Finally we show that Akt
activation may be Orai-dependent and/or TRPC-dependent, suggesting that these
ion channels could constitute a therapeutic target in cancer.