Mechanisms of multidrug resistance in cancer - PubMed (original) (raw)
Mechanisms of multidrug resistance in cancer
Jean-Pierre Gillet et al. Methods Mol Biol. 2010.
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.
Garcia-Mayea Y, Mir C, Masson F, Paciucci R, LLeonart ME. Garcia-Mayea Y, et al. 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.
Krishan A, Fitz CM, Andritsch I. Krishan A, et al. Cytometry. 1997 Dec 1;29(4):279-85. Cytometry. 1997. PMID: 9415409 Review. - Pharmacogenetics of ATP-binding cassette transporters and clinical implications.
Cascorbi I, Haenisch S. Cascorbi I, et al. 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.
Lee CH. Lee CH. Methods Mol Biol. 2010;596:325-40. doi: 10.1007/978-1-60761-416-6_14. Methods Mol Biol. 2010. PMID: 19949930 Review.
Cited by
- Serotonin-1A receptors in major depression quantified using PET: controversies, confounds, and recommendations.
Shrestha S, Hirvonen J, Hines CS, Henter ID, Svenningsson P, Pike VW, Innis RB. Shrestha S, et al. Neuroimage. 2012 Feb 15;59(4):3243-51. doi: 10.1016/j.neuroimage.2011.11.029. Epub 2011 Nov 25. Neuroimage. 2012. PMID: 22155042 Free PMC article. Review. - Melanoma Brain Metastases in the Era of Target Therapies: An Overview.
Becco P, Gallo S, Poletto S, Frascione MPM, Crotto L, Zaccagna A, Paruzzo L, Caravelli D, Carnevale-Schianca F, Aglietta M. Becco P, et al. Cancers (Basel). 2020 Jun 21;12(6):1640. doi: 10.3390/cancers12061640. Cancers (Basel). 2020. PMID: 32575838 Free PMC article. Review. - Role of membrane-embedded drug efflux ABC transporters in the cancer chemotherapy.
Gupta SK, Singh P, Ali V, Verma M. Gupta SK, et al. Oncol Rev. 2020 Jul 6;14(2):448. doi: 10.4081/oncol.2020.448. eCollection 2020 Jul 6. Oncol Rev. 2020. PMID: 32676170 Free PMC article. - Nitric oxide reverses drug resistance by inhibiting ATPase activity of p-glycoprotein in human multi-drug resistant cancer cells.
Sinha BK, Bortner CD, Mason RP, Cannon RE. Sinha BK, et al. Biochim Biophys Acta Gen Subj. 2018 Dec;1862(12):2806-2814. doi: 10.1016/j.bbagen.2018.08.021. Epub 2018 Sep 1. Biochim Biophys Acta Gen Subj. 2018. PMID: 30251669 Free PMC article. - Blockade of p38 MAPK overcomes AML stem cell line KG1a resistance to 5-Fluorouridine and the impact on miRNA profiling.
Matou-Nasri S, Najdi M, AlSaud NA, Alhaidan Y, Al-Eidi H, Alatar G, AlWadaani D, Trivilegio T, AlSubait A, AlTuwaijri A, Abudawood M, Almuzzaini B. Matou-Nasri S, et al. PLoS One. 2022 May 5;17(5):e0267855. doi: 10.1371/journal.pone.0267855. eCollection 2022. PLoS One. 2022. PMID: 35511922 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources