Molecular Mechanisms of Drug Resistance and Its Reversal in Cancer

dc.contributor.author Kartal Yandim, Melis
dc.contributor.author Adan Gökbulut, Aysun
dc.contributor.author Baran, Yusuf
dc.date.accessioned 2025-09-25T10:51:03Z
dc.date.available 2025-09-25T10:51:03Z
dc.date.issued 2016
dc.description.abstract Chemotherapy is the main strategy for the treatment of cancer. However, the main problem limiting the success of chemotherapy is the development of multidrug resistance. The resistance can be intrinsic or acquired. The resistance phenotype is associated with the tumor cells that gain a cross-resistance to a large range of drugs that are structurally and functionally different. Multidrug resistance arises via many unrelated mechanisms, such as overexpression of energy-dependent efflux proteins, decrease in uptake of the agents, increase or alteration in drug targets, modification of cell cycle checkpoints, inactivation of the agents, compartmentalization of the agents, inhibition of apoptosis and aberrant bioactive sphingolipid metabolism. Exact elucidation of resistance mechanisms and molecular and biochemical approaches to overcome multidrug resistance have been a major goal in cancer research. This review comprises the mechanisms guiding multidrug resistance in cancer chemotherapy and also touches on approaches for reversing the resistance. © 2017 Elsevier B.V., All rights reserved. en_US
dc.identifier.doi 10.3109/07388551.2015.1015957
dc.identifier.issn 1549-7801
dc.identifier.issn 0738-8551
dc.identifier.scopus 2-s2.0-84942314013
dc.identifier.uri https://doi.org/10.3109/07388551.2015.1015957
dc.identifier.uri https://hdl.handle.net/20.500.12573/4231
dc.language.iso en en_US
dc.publisher Taylor and Francis Ltd healthcare.enquiries@informa.com en_US
dc.relation.ispartof Critical Reviews in Biotechnology en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Abc Transporters en_US
dc.subject Apoptosis en_US
dc.subject Bioactive SPHingolipids en_US
dc.subject Cancer en_US
dc.subject Cell Cycle Alteration en_US
dc.subject Multidrug Resistance en_US
dc.subject Multidrug Resistance Protein en_US
dc.subject PhoSPHatidylinositol 3,4,5 TriSPhosphate 3 PhoSPHatase en_US
dc.subject Protein Bcl 2 en_US
dc.subject SPHingosine 1 Phosphate en_US
dc.subject Antineoplastic Agents en_US
dc.subject Membrane Lipids en_US
dc.subject Cell Death en_US
dc.subject Chemotherapy en_US
dc.subject Drug Therapy en_US
dc.subject Abc Transporter en_US
dc.subject Cancer en_US
dc.subject Cell Cycle en_US
dc.subject Multidrug Resistance en_US
dc.subject SPHingolipids en_US
dc.subject Diseases en_US
dc.subject Antineoplastic Agent en_US
dc.subject Breast Cancer Resistance Protein en_US
dc.subject Glucosylceramide en_US
dc.subject Membrane Lipid en_US
dc.subject Multidrug Resistance Protein en_US
dc.subject PhoSPHatidylinositol 3,4,5 TriSPhosphate 3 PhoSPHatase en_US
dc.subject Protein Bcl 2 en_US
dc.subject Protein P53 en_US
dc.subject SPHingosine 1 Phosphate en_US
dc.subject Apoptosis en_US
dc.subject Cancer Cell en_US
dc.subject Cancer Chemotherapy en_US
dc.subject Cell Compartmentalization en_US
dc.subject Clinical Trial (Topic) en_US
dc.subject Drug Accumulation en_US
dc.subject Drug Inactivation en_US
dc.subject Drug Targeting en_US
dc.subject Drug Uptake en_US
dc.subject Human en_US
dc.subject Multigene Family en_US
dc.subject Neoplasm en_US
dc.subject Phase 1 Clinical Trial (Topic) en_US
dc.subject Phase 2 Clinical Trial (Topic) en_US
dc.subject Phase 3 Clinical Trial (Topic) en_US
dc.subject Priority Journal en_US
dc.subject Review en_US
dc.subject Cell Cycle en_US
dc.subject Metabolism en_US
dc.subject Multidrug Resistance en_US
dc.subject Neoplasms en_US
dc.subject Antineoplastic Agents en_US
dc.subject Apoptosis en_US
dc.subject Cell Cycle en_US
dc.subject Drug Resistance, Multiple en_US
dc.subject Humans en_US
dc.subject Membrane Lipids en_US
dc.title Molecular Mechanisms of Drug Resistance and Its Reversal in Cancer en_US
dc.type Article en_US
dspace.entity.type Publication
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gdc.coar.access open access
gdc.coar.type text::journal::journal article
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gdc.description.department Abdullah Gül University en_US
gdc.description.departmenttemp [Kartal Yandim] Melis, Department of Molecular Biology and Genetics, Izmir Yüksek Teknoloji Enstitüsü, Izmir, Turkey; [Adan Gökbulut] Aysun, Department of Molecular Biology and Genetics, Izmir Yüksek Teknoloji Enstitüsü, Izmir, Turkey; [Baran] Yusuf, Department of Molecular Biology and Genetics, Izmir Yüksek Teknoloji Enstitüsü, Izmir, Turkey, Faculty of Life and Natural Sciences, Abdullah Gül Üniversitesi, Kayseri, Turkey en_US
gdc.description.endpage 726 en_US
gdc.description.issue 4 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q1
gdc.description.startpage 716 en_US
gdc.description.volume 36 en_US
gdc.description.wosquality Q1
gdc.identifier.openalex W1990665786
gdc.identifier.pmid 25757878
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gdc.oaire.keywords Cell cycle alteration
gdc.oaire.keywords cell cycle alteration
gdc.oaire.keywords Cell Cycle
gdc.oaire.keywords apoptosis
gdc.oaire.keywords Antineoplastic Agents
gdc.oaire.keywords Apoptosis
gdc.oaire.keywords Multidrug resistance
gdc.oaire.keywords bioactive sphingolipids
gdc.oaire.keywords Drug Resistance, Multiple
gdc.oaire.keywords Membrane Lipids
gdc.oaire.keywords ABC transporters
gdc.oaire.keywords multidrug resistance
gdc.oaire.keywords Neoplasms
gdc.oaire.keywords Bioactive sphingolipids
gdc.oaire.keywords cancer
gdc.oaire.keywords Humans
gdc.oaire.keywords Cancer
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gdc.oaire.sciencefields 0301 basic medicine
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gdc.opencitations.count 289
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gdc.scopus.citedcount 298
gdc.virtual.author Adan, Aysun
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