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Microrna let-7: an emerging next-generation cancer therapeutic
In recent years, various rna-based technologies have been under evaluation as potential next-generation cancer therapeutics. Micrornas (mirnas), known to regulate the cell cycle and development, are deregulated in various cancers. Thus, they might serve as good targets or candidates in an exploratio...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Multimed Inc.
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2826782/ https://www.ncbi.nlm.nih.gov/pubmed/20179807 |
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author | Barh, D. Malhotra, R. Ravi, B. Sindhurani, P. |
author_facet | Barh, D. Malhotra, R. Ravi, B. Sindhurani, P. |
author_sort | Barh, D. |
collection | PubMed |
description | In recent years, various rna-based technologies have been under evaluation as potential next-generation cancer therapeutics. Micrornas (mirnas), known to regulate the cell cycle and development, are deregulated in various cancers. Thus, they might serve as good targets or candidates in an exploration of anticancer therapeutics. One attractive candidate for this purpose is let-7 (“lethal-7”). Let-7 is underexpressed in various cancers, and restoration of its normal expression is found to inhibit cancer growth by targeting various oncogenes and inhibiting key regulators of several mitogenic pathways. In vivo, let-7 administration was found effective against mouse-model lung and breast cancers, and our computational prediction supports the possible effectiveness of let-7 in estrogen receptor (er)–positive metastatic breast cancer. Data also suggest that let-7 regulates apoptosis and cancer stem cell (csc) differentiation and can therefore be tested as a potential therapeutic in cancer treatment. However, the exact role of let-7 in cancer is not yet fully understood. There is a need to understand the causative molecular basis of let-7 alterations in cancer and to develop proper delivery systems before proceeding to therapeutic applications. This article attempts to highlight certain critical aspects of let-7’s therapeutic potential in cancer. |
format | Text |
id | pubmed-2826782 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Multimed Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-28267822010-02-23 Microrna let-7: an emerging next-generation cancer therapeutic Barh, D. Malhotra, R. Ravi, B. Sindhurani, P. Curr Oncol Drug Development in Contemporary Oncology In recent years, various rna-based technologies have been under evaluation as potential next-generation cancer therapeutics. Micrornas (mirnas), known to regulate the cell cycle and development, are deregulated in various cancers. Thus, they might serve as good targets or candidates in an exploration of anticancer therapeutics. One attractive candidate for this purpose is let-7 (“lethal-7”). Let-7 is underexpressed in various cancers, and restoration of its normal expression is found to inhibit cancer growth by targeting various oncogenes and inhibiting key regulators of several mitogenic pathways. In vivo, let-7 administration was found effective against mouse-model lung and breast cancers, and our computational prediction supports the possible effectiveness of let-7 in estrogen receptor (er)–positive metastatic breast cancer. Data also suggest that let-7 regulates apoptosis and cancer stem cell (csc) differentiation and can therefore be tested as a potential therapeutic in cancer treatment. However, the exact role of let-7 in cancer is not yet fully understood. There is a need to understand the causative molecular basis of let-7 alterations in cancer and to develop proper delivery systems before proceeding to therapeutic applications. This article attempts to highlight certain critical aspects of let-7’s therapeutic potential in cancer. Multimed Inc. 2010-02 /pmc/articles/PMC2826782/ /pubmed/20179807 Text en 2010 Multimed Inc. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Drug Development in Contemporary Oncology Barh, D. Malhotra, R. Ravi, B. Sindhurani, P. Microrna let-7: an emerging next-generation cancer therapeutic |
title | Microrna let-7: an emerging next-generation cancer therapeutic |
title_full | Microrna let-7: an emerging next-generation cancer therapeutic |
title_fullStr | Microrna let-7: an emerging next-generation cancer therapeutic |
title_full_unstemmed | Microrna let-7: an emerging next-generation cancer therapeutic |
title_short | Microrna let-7: an emerging next-generation cancer therapeutic |
title_sort | microrna let-7: an emerging next-generation cancer therapeutic |
topic | Drug Development in Contemporary Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2826782/ https://www.ncbi.nlm.nih.gov/pubmed/20179807 |
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