Mechanisms of multidrug resistance in cancer
- PMID: 19949920
- DOI: 10.1007/978-1-60761-416-6_4
Mechanisms of multidrug resistance in cancer
Abstract
The development of multidrug resistance (MDR) to chemotherapy remains a major challenge in the treatment of cancer. Resistance exists against every effective anticancer drug and can develop by numerous mechanisms including decreased drug uptake, increased drug efflux, activation of detoxifying systems, activation of DNA repair mechanisms, evasion of drug-induced apoptosis, etc. In the first part of this chapter, we briefly summarize the current knowledge on individual cellular mechanisms responsible for MDR, with a special emphasis on ATP-binding cassette transporters, perhaps the main theme of this textbook. Although extensive work has been done to characterize MDR mechanisms in vitro, the translation of this knowledge to the clinic has not been crowned with success. Therefore, identifying genes and mechanisms critical to the development of MDR in vivo and establishing a reliable method for analyzing clinical samples could help to predict the development of resistance and lead to treatments designed to circumvent it. Our thoughts about translational research needed to achieve significant progress in the understanding of this complex phenomenon are therefore discussed in a third section. The pleotropic response of cancer cells to chemotherapy is summarized in a concluding diagram.
Similar articles
-
Insights into new mechanisms and models of cancer stem cell multidrug resistance.Semin Cancer Biol. 2020 Feb;60:166-180. doi: 10.1016/j.semcancer.2019.07.022. Epub 2019 Jul 29. Semin Cancer Biol. 2020. PMID: 31369817 Review.
-
Drug retention, efflux, and resistance in tumor cells.Cytometry. 1997 Dec 1;29(4):279-85. Cytometry. 1997. PMID: 9415409 Review.
-
Pharmacogenetics of ATP-binding cassette transporters and clinical implications.Methods Mol Biol. 2010;596:95-121. doi: 10.1007/978-1-60761-416-6_6. Methods Mol Biol. 2010. PMID: 19949922
-
Reversing agents for ATP-binding cassette drug transporters.Methods Mol Biol. 2010;596:325-40. doi: 10.1007/978-1-60761-416-6_14. Methods Mol Biol. 2010. PMID: 19949930 Review.
-
Modulation of function of three ABC drug transporters, P-glycoprotein (ABCB1), mitoxantrone resistance protein (ABCG2) and multidrug resistance protein 1 (ABCC1) by tetrahydrocurcumin, a major metabolite of curcumin.Mol Cell Biochem. 2007 Feb;296(1-2):85-95. doi: 10.1007/s11010-006-9302-8. Epub 2006 Sep 8. Mol Cell Biochem. 2007. PMID: 16960658
Cited by
-
New Dual P-Glycoprotein (P-gp) and Human Carbonic Anhydrase XII (hCA XII) Inhibitors as Multidrug Resistance (MDR) Reversers in Cancer Cells.J Med Chem. 2022 Nov 10;65(21):14655-14672. doi: 10.1021/acs.jmedchem.2c01175. Epub 2022 Oct 21. J Med Chem. 2022. PMID: 36269278 Free PMC article.
-
mRNA overexpression of BAALC: A novel prognostic factor for pediatric acute lymphoblastic leukemia.Biomed Rep. 2015 May;3(3):371-374. doi: 10.3892/br.2015.437. Epub 2015 Feb 26. Biomed Rep. 2015. PMID: 26137238 Free PMC article.
-
Biodegradable mixed MPEG-SS-2SA/TPGS micelles for triggered intracellular release of paclitaxel and reversing multidrug resistance.Int J Nanomedicine. 2016 Oct 6;11:5109-5123. doi: 10.2147/IJN.S111930. eCollection 2016. Int J Nanomedicine. 2016. PMID: 27785018 Free PMC article.
-
Cancer stem cells and strategies for targeted drug delivery.Drug Deliv Transl Res. 2021 Oct;11(5):1779-1805. doi: 10.1007/s13346-020-00863-9. Epub 2020 Oct 23. Drug Deliv Transl Res. 2021. PMID: 33095384 Free PMC article. Review.
-
Hydroxygenkwanin Improves the Efficacy of Cytotoxic Drugs in ABCG2-Overexpressing Multidrug-Resistant Cancer Cells.Int J Mol Sci. 2022 Oct 23;23(21):12763. doi: 10.3390/ijms232112763. Int J Mol Sci. 2022. PMID: 36361555 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources