Advances in understanding the role of P-gp in doxorubicin resistance: molecular pathways, therapeutic strategies, and prospects
dc.authorid | Ali Zarrabi / 0000-0003-0391-1769 | en_US |
dc.authorscopusid | Ali Zarrabi / 23483174100 | en_US |
dc.authorwosid | Ali Zarrabi / U-2602-2019 | |
dc.contributor.author | Mirzaei, Sepideh | |
dc.contributor.author | Gholami, Mohammad Hossein | |
dc.contributor.author | Hashemi, Farid | |
dc.contributor.author | Zabolian, Amirhossein | |
dc.contributor.author | Zarrabi, Ali | |
dc.date.accessioned | 2021-11-08T07:15:26Z | |
dc.date.available | 2021-11-08T07:15:26Z | |
dc.date.issued | 2022 | en_US |
dc.department | İstinye Üniversitesi, Mühendislik ve Doğa Bilimleri Fakültesi, Biyomedikal Mühendisliği Bölümü | en_US |
dc.description.abstract | P-glycoprotein (P-gp) is a drug efflux transporter that triggers doxorubicin (DOX) resistance. In this review, we highlight the molecular avenues regulating P-gp, such as Nrf2, HIF-1?, miRNAs, and long noncoding (lnc)RNAs, to reveal their participation in DOX resistance. These antitumor compounds and genetic tools synergistically reduce P-gp expression. Furthermore, ATP depletion impairs P-gp activity to enhance the antitumor activity of DOX. Nanoarchitectures, including liposomes, micelles, polymeric nanoparticles (NPs), and solid lipid nanocarriers, have been developed for the co-delivery of DOX with anticancer compounds and genes enhancing DOX cytotoxicity. Surface modification of nanocarriers, for instance with hyaluronic acid (HA), can promote selectivity toward cancer cells. We discuss these aspects with a focus on P-gp expression and activity. © 2021 The Author(s) | en_US |
dc.identifier.citation | Mirzaei, S., Gholami, M. H., Hashemi, F., Zabolian, A., Farahani, M. V., Hushmandi, K., ... & Orive, G. (2021). Advances in understanding the role of P-gp in doxorubicin resistance: Molecular pathways, therapeutic strategies, and prospects. Drug Discovery Today.10.1016/j.drudis.2021.09.020. | en_US |
dc.identifier.doi | 10.1016/j.drudis.2021.09.020 | en_US |
dc.identifier.endpage | 20 | en_US |
dc.identifier.issn | 1359-6446 | en_US |
dc.identifier.pmid | 34624510 | en_US |
dc.identifier.scopus | 2-s2.0-85117840070 | en_US |
dc.identifier.scopusquality | Q1 | en_US |
dc.identifier.startpage | 1 | en_US |
dc.identifier.uri | https://doi.org/10.1016/j.drudis.2021.09.020 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12713/2203 | |
dc.identifier.wos | WOS:000750040900008 | en_US |
dc.identifier.wosquality | Q1 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.institutionauthor | Zarrabi, Ali | |
dc.language.iso | en | en_US |
dc.publisher | Elsevier | en_US |
dc.relation.ispartof | Drug Discovery Today | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.title | Advances in understanding the role of P-gp in doxorubicin resistance: molecular pathways, therapeutic strategies, and prospects | en_US |
dc.type | Article | en_US |