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Review ArticleR

Death by Design: Where Curcumin Sensitizes Drug-resistant Tumours

SHILPI SAHA, ARGHYA ADHIKARY, PUSHPAK BHATTACHARYYA, TANYA DAS and GAURISANKAR SA
Anticancer Research July 2012, 32 (7) 2567-2584;
SHILPI SAHA
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ARGHYA ADHIKARY
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PUSHPAK BHATTACHARYYA
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TANYA DAS
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  • For correspondence: gauri@bic.boseinst.ernet.in tanya@bic.boseinst.ernet.in
GAURISANKAR SA
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  • For correspondence: gauri@bic.boseinst.ernet.in tanya@bic.boseinst.ernet.in
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Abstract

Chemotherapy remains the core of anticancer treatment. However, despite the tremendous strides made in the development of targeted anticancer therapies, emergence of resistance to chemotherapeutic drugs is still a major obstacle in the successful management of resistant tumours. Therefore, profound investigation into the in-depth molecular mechanisms of drug resistance is essential and may hopefully translate into effective therapies that can flip the switch from drug resistance to susceptibility. Mechanistically, resistance phenomena may be explained by (i) overexpression of drug efflux pumps, (ii) enhanced drug detoxification, (iii) rapid DNA repair efficiency, (iv) defects in apoptosis regulation, and (v) active cell survival signals. Several adverse effects associated with multidrug resistance and the need for safe multi-targeted anticancer drugs instigated the use of the phytochemical, curcumin, the yellow pigment of the spice turmeric, which has pleotropic activities. We performed a structured literature review using PubMed and Medline searches with secondary review of cited publications, identifying studies on the role of curcumin in conquering drug resistance in cancer. This review describes how curcumin sensitizes cancer cells through regulation of multiple multidrug resistance pathways, thus employing one drug for multiple targets. Curcumin helps the cancer cells to regain their ‘forgotten’ apoptosis, modulates drug-target interaction at different levels, restrains survival pathways when their proteins are overexpressed, and finds an alternate way to carry forward the process of sensitization of different resistant tumours. Additionally, the review dissects the role of curcumin, if any, in targeting the major culprit of drug resistance, cancer stem cells (CSC), thereby circumventing resistance. Taken together, this review strongly suggests that curcumin is a promising chemosensitizing agent and that the unique properties of curcumin may be exploited for successful management of resistant tumours.

  • Curcumin
  • drug efflux pumps
  • multidrug resistance
  • NFκB
  • p300
  • p53
  • review
  • Received April 30, 2012.
  • Revision received May 29, 2012.
  • Accepted May 30, 2012.
  • Copyright© 2012 International Institute of Anticancer Research (Dr. John G. Delinassios), All rights reserved
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Anticancer Research: 32 (7)
Anticancer Research
Vol. 32, Issue 7
July 2012
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Death by Design: Where Curcumin Sensitizes Drug-resistant Tumours
SHILPI SAHA, ARGHYA ADHIKARY, PUSHPAK BHATTACHARYYA, TANYA DAS, GAURISANKAR SA
Anticancer Research Jul 2012, 32 (7) 2567-2584;

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Death by Design: Where Curcumin Sensitizes Drug-resistant Tumours
SHILPI SAHA, ARGHYA ADHIKARY, PUSHPAK BHATTACHARYYA, TANYA DAS, GAURISANKAR SA
Anticancer Research Jul 2012, 32 (7) 2567-2584;
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  • Article
    • Abstract
    • MDR: Major Hurdle in Designing Death
    • The Canvas of Drug Resistance
    • Phytochemicals in Redesigning the Landscape of Drug Resistance
    • Curcumin Architects the Chemosensitization Programme
    • Curcumin as apoptosis inducer
    • Curcumin as a chemosensitizer
    • Cancer Stem Cells: New Colour in Drug-Resistance
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