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Curcumin Nanoformulations for Colorectal Cancer: A Review

Colorectal cancer (CRC) is the third most prevalent form of cancer, after lung cancer and breast cancer, with the second highest death incidence. Over the years, natural compounds have been explored as an alternative to conventional cancer therapies such as surgery, radiotherapy, and chemotherapy. C...

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Autores principales: Wong, Kar En, Ngai, Siew Ching, Chan, Kok-Gan, Lee, Learn-Han, Goh, Bey-Hing, Chuah, Lay-Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6412150/
https://www.ncbi.nlm.nih.gov/pubmed/30890933
http://dx.doi.org/10.3389/fphar.2019.00152
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author Wong, Kar En
Ngai, Siew Ching
Chan, Kok-Gan
Lee, Learn-Han
Goh, Bey-Hing
Chuah, Lay-Hong
author_facet Wong, Kar En
Ngai, Siew Ching
Chan, Kok-Gan
Lee, Learn-Han
Goh, Bey-Hing
Chuah, Lay-Hong
author_sort Wong, Kar En
collection PubMed
description Colorectal cancer (CRC) is the third most prevalent form of cancer, after lung cancer and breast cancer, with the second highest death incidence. Over the years, natural compounds have been explored as an alternative to conventional cancer therapies such as surgery, radiotherapy, and chemotherapy. Curcumin, an active constituent of turmeric has been associated with various health benefits. It has gained much attention as an anticancer agent due to its ability to regulate multiple cell signaling pathways, including NF-κB, STAT3, activated protein-1 (AP-1), epidermal growth response-1 (Egr-1), and p53, which are crucial in cancer development and progression. Nevertheless, the clinical application of curcumin is greatly restricted because of its low water solubility, poor oral absorption, and rapid metabolism. These issues have led to the development of curcumin nanoformulations to overcome the limitations of the compound. Nanotechnology-based delivery systems have been widely used in improving the delivery of poorly-water soluble drugs. Besides, these systems also come with the added benefits of possible cellular targeting and improvement in cellular uptake. An ideal improved formulation should display a greater anticancer activity compared to free curcumin, and at the same time be non-toxic to the normal cells. In this review, we focus on the design and development of various nanoformulations to deliver curcumin for use in CRC such as liposomes, micelles, polymer nanoparticles, nanogels, cyclodextrin complexes, solid lipid nanoparticles (SLN), phytosomes, and gold nanoparticles. We also discuss the current pre-clinical and clinical evidences of curcumin nanoformulations in CRC therapy, analyse the research gap, and address the future direction of this research area.
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spelling pubmed-64121502019-03-19 Curcumin Nanoformulations for Colorectal Cancer: A Review Wong, Kar En Ngai, Siew Ching Chan, Kok-Gan Lee, Learn-Han Goh, Bey-Hing Chuah, Lay-Hong Front Pharmacol Pharmacology Colorectal cancer (CRC) is the third most prevalent form of cancer, after lung cancer and breast cancer, with the second highest death incidence. Over the years, natural compounds have been explored as an alternative to conventional cancer therapies such as surgery, radiotherapy, and chemotherapy. Curcumin, an active constituent of turmeric has been associated with various health benefits. It has gained much attention as an anticancer agent due to its ability to regulate multiple cell signaling pathways, including NF-κB, STAT3, activated protein-1 (AP-1), epidermal growth response-1 (Egr-1), and p53, which are crucial in cancer development and progression. Nevertheless, the clinical application of curcumin is greatly restricted because of its low water solubility, poor oral absorption, and rapid metabolism. These issues have led to the development of curcumin nanoformulations to overcome the limitations of the compound. Nanotechnology-based delivery systems have been widely used in improving the delivery of poorly-water soluble drugs. Besides, these systems also come with the added benefits of possible cellular targeting and improvement in cellular uptake. An ideal improved formulation should display a greater anticancer activity compared to free curcumin, and at the same time be non-toxic to the normal cells. In this review, we focus on the design and development of various nanoformulations to deliver curcumin for use in CRC such as liposomes, micelles, polymer nanoparticles, nanogels, cyclodextrin complexes, solid lipid nanoparticles (SLN), phytosomes, and gold nanoparticles. We also discuss the current pre-clinical and clinical evidences of curcumin nanoformulations in CRC therapy, analyse the research gap, and address the future direction of this research area. Frontiers Media S.A. 2019-03-05 /pmc/articles/PMC6412150/ /pubmed/30890933 http://dx.doi.org/10.3389/fphar.2019.00152 Text en Copyright © 2019 Wong, Ngai, Chan, Lee, Goh and Chuah. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Wong, Kar En
Ngai, Siew Ching
Chan, Kok-Gan
Lee, Learn-Han
Goh, Bey-Hing
Chuah, Lay-Hong
Curcumin Nanoformulations for Colorectal Cancer: A Review
title Curcumin Nanoformulations for Colorectal Cancer: A Review
title_full Curcumin Nanoformulations for Colorectal Cancer: A Review
title_fullStr Curcumin Nanoformulations for Colorectal Cancer: A Review
title_full_unstemmed Curcumin Nanoformulations for Colorectal Cancer: A Review
title_short Curcumin Nanoformulations for Colorectal Cancer: A Review
title_sort curcumin nanoformulations for colorectal cancer: a review
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6412150/
https://www.ncbi.nlm.nih.gov/pubmed/30890933
http://dx.doi.org/10.3389/fphar.2019.00152
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