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Natural Alkaloids and Heterocycles as G-Quadruplex Ligands and Potential Anticancer Agents
G-quadruplexes are four-stranded nucleic acid secondary structures that are formed in guanine-rich sequences. G-quadruplexes are widely distributed in functional regions of the human genome and transcriptome, such as human telomeres, oncogene promoter regions, replication initiation sites, and untra...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017894/ https://www.ncbi.nlm.nih.gov/pubmed/29473874 http://dx.doi.org/10.3390/molecules23020493 |
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author | Che, Tong Wang, Yu-Qing Huang, Zhou-Li Tan, Jia-Heng Huang, Zhi-Shu Chen, Shuo-Bin |
author_facet | Che, Tong Wang, Yu-Qing Huang, Zhou-Li Tan, Jia-Heng Huang, Zhi-Shu Chen, Shuo-Bin |
author_sort | Che, Tong |
collection | PubMed |
description | G-quadruplexes are four-stranded nucleic acid secondary structures that are formed in guanine-rich sequences. G-quadruplexes are widely distributed in functional regions of the human genome and transcriptome, such as human telomeres, oncogene promoter regions, replication initiation sites, and untranslated regions. Many G-quadruplex-forming sequences are found to be associated with cancer, and thus, these non-canonical nucleic acid structures are considered to be attractive molecular targets for cancer therapeutics with novel mechanisms of action. In this mini review, we summarize recent advances made by our lab in the study of G-quadruplex-targeted natural alkaloids and their derivatives toward the development of potential anticancer agents. |
format | Online Article Text |
id | pubmed-6017894 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-60178942018-11-13 Natural Alkaloids and Heterocycles as G-Quadruplex Ligands and Potential Anticancer Agents Che, Tong Wang, Yu-Qing Huang, Zhou-Li Tan, Jia-Heng Huang, Zhi-Shu Chen, Shuo-Bin Molecules Review G-quadruplexes are four-stranded nucleic acid secondary structures that are formed in guanine-rich sequences. G-quadruplexes are widely distributed in functional regions of the human genome and transcriptome, such as human telomeres, oncogene promoter regions, replication initiation sites, and untranslated regions. Many G-quadruplex-forming sequences are found to be associated with cancer, and thus, these non-canonical nucleic acid structures are considered to be attractive molecular targets for cancer therapeutics with novel mechanisms of action. In this mini review, we summarize recent advances made by our lab in the study of G-quadruplex-targeted natural alkaloids and their derivatives toward the development of potential anticancer agents. MDPI 2018-02-23 /pmc/articles/PMC6017894/ /pubmed/29473874 http://dx.doi.org/10.3390/molecules23020493 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Che, Tong Wang, Yu-Qing Huang, Zhou-Li Tan, Jia-Heng Huang, Zhi-Shu Chen, Shuo-Bin Natural Alkaloids and Heterocycles as G-Quadruplex Ligands and Potential Anticancer Agents |
title | Natural Alkaloids and Heterocycles as G-Quadruplex Ligands and Potential Anticancer Agents |
title_full | Natural Alkaloids and Heterocycles as G-Quadruplex Ligands and Potential Anticancer Agents |
title_fullStr | Natural Alkaloids and Heterocycles as G-Quadruplex Ligands and Potential Anticancer Agents |
title_full_unstemmed | Natural Alkaloids and Heterocycles as G-Quadruplex Ligands and Potential Anticancer Agents |
title_short | Natural Alkaloids and Heterocycles as G-Quadruplex Ligands and Potential Anticancer Agents |
title_sort | natural alkaloids and heterocycles as g-quadruplex ligands and potential anticancer agents |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017894/ https://www.ncbi.nlm.nih.gov/pubmed/29473874 http://dx.doi.org/10.3390/molecules23020493 |
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