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      Molecular mechanisms of drug resistance and its reversal in cancer.

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          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.

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          Author and article information

          Journal
          Crit. Rev. Biotechnol.
          Critical reviews in biotechnology
          Informa UK Limited
          1549-7801
          0738-8551
          Aug 2016
          : 36
          : 4
          Affiliations
          [1 ] a Department of Molecular Biology and Genetics , İzmir Institute of Technology , Urla , İzmir , Turkey and.
          [2 ] b Faculty of Life and Natural Sciences , Abdullah Gul University , Kayseri , Turkey.
          Article
          10.3109/07388551.2015.1015957
          25757878
          fada7503-5b30-4595-9325-8694e12278f7
          History

          multidrug resistance,ABC transporters,apoptosis,bioactive sphingolipids,cancer,cell cycle alteration

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