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miR-33a is a tumor suppressor microRNA that is decreased in prostate cancer
Prostate cancer is one of the most frequently diagnosed neoplasms among men worldwide. MicroRNAs (miRNAs) are involved in numerous important cellular processes including proliferation, differentiation and apoptosis. They have been found to be aberrantly expressed in many types of human cancers. They...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601135/ https://www.ncbi.nlm.nih.gov/pubmed/28947967 http://dx.doi.org/10.18632/oncotarget.19521 |
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author | Karatas, Omer Faruk Wang, Jianghua Shao, Longjiang Ozen, Mustafa Zhang, Yiqun Creighton, Chad J. Ittmann, Michael |
author_facet | Karatas, Omer Faruk Wang, Jianghua Shao, Longjiang Ozen, Mustafa Zhang, Yiqun Creighton, Chad J. Ittmann, Michael |
author_sort | Karatas, Omer Faruk |
collection | PubMed |
description | Prostate cancer is one of the most frequently diagnosed neoplasms among men worldwide. MicroRNAs (miRNAs) are involved in numerous important cellular processes including proliferation, differentiation and apoptosis. They have been found to be aberrantly expressed in many types of human cancers. They can act as either tumor suppressors or oncogenes, and changes in their levels are associated with tumor initiation, progression and metastasis. miR-33a is an intronic miRNA embedded within SREBF2 that has been reported to have tumor suppressive properties in some cancers but has not been examined in prostate cancer. SREBF2 increases cholesterol and lipid levels both directly and via miR-33a action. The levels of SREBF2 and miR-33a are correlated in normal tissues by co-transcription from the same gene locus. Paradoxically, SREBF2 has been reported to be increased in prostate cancer, which would be predicted to increase miR-33a levels potentially leading to tumor suppression. We show here that miR-33a has tumor suppressive activities and is decreased in prostate cancer. The decreased miR-33a increases mRNA for the PIM1 oncogene and multiple genes in the lipid β-oxidation pathway. Levels of miR-33a are not correlated with SREBF2 levels, implying posttranscriptional regulation of its expression in prostate cancer. |
format | Online Article Text |
id | pubmed-5601135 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-56011352017-09-25 miR-33a is a tumor suppressor microRNA that is decreased in prostate cancer Karatas, Omer Faruk Wang, Jianghua Shao, Longjiang Ozen, Mustafa Zhang, Yiqun Creighton, Chad J. Ittmann, Michael Oncotarget Research Paper Prostate cancer is one of the most frequently diagnosed neoplasms among men worldwide. MicroRNAs (miRNAs) are involved in numerous important cellular processes including proliferation, differentiation and apoptosis. They have been found to be aberrantly expressed in many types of human cancers. They can act as either tumor suppressors or oncogenes, and changes in their levels are associated with tumor initiation, progression and metastasis. miR-33a is an intronic miRNA embedded within SREBF2 that has been reported to have tumor suppressive properties in some cancers but has not been examined in prostate cancer. SREBF2 increases cholesterol and lipid levels both directly and via miR-33a action. The levels of SREBF2 and miR-33a are correlated in normal tissues by co-transcription from the same gene locus. Paradoxically, SREBF2 has been reported to be increased in prostate cancer, which would be predicted to increase miR-33a levels potentially leading to tumor suppression. We show here that miR-33a has tumor suppressive activities and is decreased in prostate cancer. The decreased miR-33a increases mRNA for the PIM1 oncogene and multiple genes in the lipid β-oxidation pathway. Levels of miR-33a are not correlated with SREBF2 levels, implying posttranscriptional regulation of its expression in prostate cancer. Impact Journals LLC 2017-07-24 /pmc/articles/PMC5601135/ /pubmed/28947967 http://dx.doi.org/10.18632/oncotarget.19521 Text en Copyright: © 2017 Karatas et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Research Paper Karatas, Omer Faruk Wang, Jianghua Shao, Longjiang Ozen, Mustafa Zhang, Yiqun Creighton, Chad J. Ittmann, Michael miR-33a is a tumor suppressor microRNA that is decreased in prostate cancer |
title | miR-33a is a tumor suppressor microRNA that is decreased in prostate cancer |
title_full | miR-33a is a tumor suppressor microRNA that is decreased in prostate cancer |
title_fullStr | miR-33a is a tumor suppressor microRNA that is decreased in prostate cancer |
title_full_unstemmed | miR-33a is a tumor suppressor microRNA that is decreased in prostate cancer |
title_short | miR-33a is a tumor suppressor microRNA that is decreased in prostate cancer |
title_sort | mir-33a is a tumor suppressor microrna that is decreased in prostate cancer |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601135/ https://www.ncbi.nlm.nih.gov/pubmed/28947967 http://dx.doi.org/10.18632/oncotarget.19521 |
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