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Current Status on Marine Products with Reversal Effect on Cancer Multidrug Resistance

The resistance of tumor cells to a broad range of anticancer agents continues to be a problem for the success of cancer chemotherapy. Multidrug resistance (MDR) is due in part to three drug transporter proteins: ABCB1/P-glycoprotein (P-gp), ABCC1/multidrug resistance protein 1 (MRP1) and ABCG2/breas...

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Autores principales: Abraham, Ioana, El Sayed, Khalid, Chen, Zhe-Sheng, Guo, Huiqin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3497025/
https://www.ncbi.nlm.nih.gov/pubmed/23170086
http://dx.doi.org/10.3390/md10102312
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author Abraham, Ioana
El Sayed, Khalid
Chen, Zhe-Sheng
Guo, Huiqin
author_facet Abraham, Ioana
El Sayed, Khalid
Chen, Zhe-Sheng
Guo, Huiqin
author_sort Abraham, Ioana
collection PubMed
description The resistance of tumor cells to a broad range of anticancer agents continues to be a problem for the success of cancer chemotherapy. Multidrug resistance (MDR) is due in part to three drug transporter proteins: ABCB1/P-glycoprotein (P-gp), ABCC1/multidrug resistance protein 1 (MRP1) and ABCG2/breast cancer resistance protein (BCRP). These transporters are part of the ATP-binding cassette (ABC) superfamily, whose members function as ATP-dependent drug-efflux pumps. Their activity can be blocked by various drugs such as verapamil (calcium channel blocker) and cyclosporin A (immunosuppressive agent), etc. These compounds are called MDR modulators or reversals. This review highlights several marine natural products with reversal effect on multidrug resistance in cancer, including agosterol A, ecteinascidin 743, sipholane triterpenoids, bryostatin 1, and welwitindolinones.
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spelling pubmed-34970252012-11-20 Current Status on Marine Products with Reversal Effect on Cancer Multidrug Resistance Abraham, Ioana El Sayed, Khalid Chen, Zhe-Sheng Guo, Huiqin Mar Drugs Review The resistance of tumor cells to a broad range of anticancer agents continues to be a problem for the success of cancer chemotherapy. Multidrug resistance (MDR) is due in part to three drug transporter proteins: ABCB1/P-glycoprotein (P-gp), ABCC1/multidrug resistance protein 1 (MRP1) and ABCG2/breast cancer resistance protein (BCRP). These transporters are part of the ATP-binding cassette (ABC) superfamily, whose members function as ATP-dependent drug-efflux pumps. Their activity can be blocked by various drugs such as verapamil (calcium channel blocker) and cyclosporin A (immunosuppressive agent), etc. These compounds are called MDR modulators or reversals. This review highlights several marine natural products with reversal effect on multidrug resistance in cancer, including agosterol A, ecteinascidin 743, sipholane triterpenoids, bryostatin 1, and welwitindolinones. MDPI 2012-10-19 /pmc/articles/PMC3497025/ /pubmed/23170086 http://dx.doi.org/10.3390/md10102312 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Abraham, Ioana
El Sayed, Khalid
Chen, Zhe-Sheng
Guo, Huiqin
Current Status on Marine Products with Reversal Effect on Cancer Multidrug Resistance
title Current Status on Marine Products with Reversal Effect on Cancer Multidrug Resistance
title_full Current Status on Marine Products with Reversal Effect on Cancer Multidrug Resistance
title_fullStr Current Status on Marine Products with Reversal Effect on Cancer Multidrug Resistance
title_full_unstemmed Current Status on Marine Products with Reversal Effect on Cancer Multidrug Resistance
title_short Current Status on Marine Products with Reversal Effect on Cancer Multidrug Resistance
title_sort current status on marine products with reversal effect on cancer multidrug resistance
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3497025/
https://www.ncbi.nlm.nih.gov/pubmed/23170086
http://dx.doi.org/10.3390/md10102312
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