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Fatty acid synthase is a primary target of MiR-15a and MiR-16-1 in breast cancer
Fatty acid synthase (FASN) is upregulated in breast cancer and correlates with poor prognosis. FASN contributes to mammary oncogenesis and serves as a bona fide target in cancer therapies. MicroRNAs inhibit gene expression through blocking mRNA translation or promoting mRNA degradation by targeting...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5346660/ https://www.ncbi.nlm.nih.gov/pubmed/27713175 http://dx.doi.org/10.18632/oncotarget.12479 |
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author | Wang, Jingxuan Zhang, Xiao Shi, Jinming Cao, Paul Wan, Meimei Zhang, Qiang Wang, Yunxuan Kridel, Steven J. Liu, Wennuan Xu, Jianfeng Zhang, Qingyuan Sui, Guangchao |
author_facet | Wang, Jingxuan Zhang, Xiao Shi, Jinming Cao, Paul Wan, Meimei Zhang, Qiang Wang, Yunxuan Kridel, Steven J. Liu, Wennuan Xu, Jianfeng Zhang, Qingyuan Sui, Guangchao |
author_sort | Wang, Jingxuan |
collection | PubMed |
description | Fatty acid synthase (FASN) is upregulated in breast cancer and correlates with poor prognosis. FASN contributes to mammary oncogenesis and serves as a bona fide target in cancer therapies. MicroRNAs inhibit gene expression through blocking mRNA translation or promoting mRNA degradation by targeting their 3′-UTRs. We identified four microRNAs in two microRNA clusters miR-15a-16-1 and miR-497-195 that share a common seed sequence to target the 3′-UTR of the FASN mRNA. In reporter assays, both of these microRNA clusters inhibited the expression of a reporter construct containing the FASN 3′-UTR. However, only ectopic miR-15a-16-1, but not miR-497-195, markedly reduced the levels of endogenous FASN in breast cancer cells. Both miR-15a and miR-16-1 contributes to inhibiting FASN expression and breast cancer cell proliferation. Consistently, a sponge construct consisting of eight repeats of the FASN 3′-UTR region targeted by these microRNAs could markedly increase endogenous FASN levels in mammary cells. When FASN expression was restored by ectopic expression in breast cancer cells, retarded cell proliferation caused by miR-15a-16-1 was partially rescued. In conclusion, we demonstrated that FASN expression is primarily downregulated by miR-15a and miR-16-1 in mammary cells and FASN is one of the major targets of these two tumor suppressive microRNAs. |
format | Online Article Text |
id | pubmed-5346660 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53466602017-03-30 Fatty acid synthase is a primary target of MiR-15a and MiR-16-1 in breast cancer Wang, Jingxuan Zhang, Xiao Shi, Jinming Cao, Paul Wan, Meimei Zhang, Qiang Wang, Yunxuan Kridel, Steven J. Liu, Wennuan Xu, Jianfeng Zhang, Qingyuan Sui, Guangchao Oncotarget Research Paper Fatty acid synthase (FASN) is upregulated in breast cancer and correlates with poor prognosis. FASN contributes to mammary oncogenesis and serves as a bona fide target in cancer therapies. MicroRNAs inhibit gene expression through blocking mRNA translation or promoting mRNA degradation by targeting their 3′-UTRs. We identified four microRNAs in two microRNA clusters miR-15a-16-1 and miR-497-195 that share a common seed sequence to target the 3′-UTR of the FASN mRNA. In reporter assays, both of these microRNA clusters inhibited the expression of a reporter construct containing the FASN 3′-UTR. However, only ectopic miR-15a-16-1, but not miR-497-195, markedly reduced the levels of endogenous FASN in breast cancer cells. Both miR-15a and miR-16-1 contributes to inhibiting FASN expression and breast cancer cell proliferation. Consistently, a sponge construct consisting of eight repeats of the FASN 3′-UTR region targeted by these microRNAs could markedly increase endogenous FASN levels in mammary cells. When FASN expression was restored by ectopic expression in breast cancer cells, retarded cell proliferation caused by miR-15a-16-1 was partially rescued. In conclusion, we demonstrated that FASN expression is primarily downregulated by miR-15a and miR-16-1 in mammary cells and FASN is one of the major targets of these two tumor suppressive microRNAs. Impact Journals LLC 2016-10-05 /pmc/articles/PMC5346660/ /pubmed/27713175 http://dx.doi.org/10.18632/oncotarget.12479 Text en Copyright: © 2016 Wang et al. http://creativecommons.org/licenses/by/3.0/ 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 author and source are credited. |
spellingShingle | Research Paper Wang, Jingxuan Zhang, Xiao Shi, Jinming Cao, Paul Wan, Meimei Zhang, Qiang Wang, Yunxuan Kridel, Steven J. Liu, Wennuan Xu, Jianfeng Zhang, Qingyuan Sui, Guangchao Fatty acid synthase is a primary target of MiR-15a and MiR-16-1 in breast cancer |
title | Fatty acid synthase is a primary target of MiR-15a and MiR-16-1 in breast cancer |
title_full | Fatty acid synthase is a primary target of MiR-15a and MiR-16-1 in breast cancer |
title_fullStr | Fatty acid synthase is a primary target of MiR-15a and MiR-16-1 in breast cancer |
title_full_unstemmed | Fatty acid synthase is a primary target of MiR-15a and MiR-16-1 in breast cancer |
title_short | Fatty acid synthase is a primary target of MiR-15a and MiR-16-1 in breast cancer |
title_sort | fatty acid synthase is a primary target of mir-15a and mir-16-1 in breast cancer |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5346660/ https://www.ncbi.nlm.nih.gov/pubmed/27713175 http://dx.doi.org/10.18632/oncotarget.12479 |
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