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MicroRNA-203 functions as a tumor suppressor in basal cell carcinoma
Basal cell carcinoma (BCC) of the skin represents the most common malignancy in humans. MicroRNAs (miRNAs), small regulatory RNAs with pleiotropic function, are commonly misregulated in cancer. Here we identify miR-203, a miRNA abundantly and preferentially expressed in skin, to be downregulated in...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3412636/ https://www.ncbi.nlm.nih.gov/pubmed/23552555 http://dx.doi.org/10.1038/oncsis.2012.3 |
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author | Sonkoly, E Lovén, J Xu, N Meisgen, F Wei, T Brodin, P Jaks, V Kasper, M Shimokawa, T Harada, M Heilborn, J Hedblad, M-A Hippe, A Grandér, D Homey, B Zaphiropoulos, P G Arsenian-Henriksson, M Ståhle, M Pivarcsi, A |
author_facet | Sonkoly, E Lovén, J Xu, N Meisgen, F Wei, T Brodin, P Jaks, V Kasper, M Shimokawa, T Harada, M Heilborn, J Hedblad, M-A Hippe, A Grandér, D Homey, B Zaphiropoulos, P G Arsenian-Henriksson, M Ståhle, M Pivarcsi, A |
author_sort | Sonkoly, E |
collection | PubMed |
description | Basal cell carcinoma (BCC) of the skin represents the most common malignancy in humans. MicroRNAs (miRNAs), small regulatory RNAs with pleiotropic function, are commonly misregulated in cancer. Here we identify miR-203, a miRNA abundantly and preferentially expressed in skin, to be downregulated in BCCs. We show that activation of the Hedgehog (HH) pathway, critically involved in the pathogenesis of BCCs, as well as the EGFR/MEK/ERK/c-JUN signaling pathway suppresses miR-203. We identify c-JUN, a key effector of the HH pathway, as a novel direct target for miR-203 in vivo. Further supporting the role of miR-203 as a tumor suppressor, in vivo delivery of miR-203 mimics in a BCC mouse model results in the reduction of tumor growth. Our results identify a regulatory circuit involving miR-203 and c-JUN, which provides functional control over basal cell proliferation and differentiation. We propose that miR-203 functions as a ‘bona fide' tumor suppressor in BCC, whose suppressed expression contributes to oncogenic transformation via derepression of multiple stemness- and proliferation-related genes, and its overexpression could be of therapeutic value. |
format | Online Article Text |
id | pubmed-3412636 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-34126362012-08-13 MicroRNA-203 functions as a tumor suppressor in basal cell carcinoma Sonkoly, E Lovén, J Xu, N Meisgen, F Wei, T Brodin, P Jaks, V Kasper, M Shimokawa, T Harada, M Heilborn, J Hedblad, M-A Hippe, A Grandér, D Homey, B Zaphiropoulos, P G Arsenian-Henriksson, M Ståhle, M Pivarcsi, A Oncogenesis Original Article Basal cell carcinoma (BCC) of the skin represents the most common malignancy in humans. MicroRNAs (miRNAs), small regulatory RNAs with pleiotropic function, are commonly misregulated in cancer. Here we identify miR-203, a miRNA abundantly and preferentially expressed in skin, to be downregulated in BCCs. We show that activation of the Hedgehog (HH) pathway, critically involved in the pathogenesis of BCCs, as well as the EGFR/MEK/ERK/c-JUN signaling pathway suppresses miR-203. We identify c-JUN, a key effector of the HH pathway, as a novel direct target for miR-203 in vivo. Further supporting the role of miR-203 as a tumor suppressor, in vivo delivery of miR-203 mimics in a BCC mouse model results in the reduction of tumor growth. Our results identify a regulatory circuit involving miR-203 and c-JUN, which provides functional control over basal cell proliferation and differentiation. We propose that miR-203 functions as a ‘bona fide' tumor suppressor in BCC, whose suppressed expression contributes to oncogenic transformation via derepression of multiple stemness- and proliferation-related genes, and its overexpression could be of therapeutic value. Nature Publishing Group 2012-03 2012-03-12 /pmc/articles/PMC3412636/ /pubmed/23552555 http://dx.doi.org/10.1038/oncsis.2012.3 Text en Copyright © 2012 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-No Derivative Works 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Original Article Sonkoly, E Lovén, J Xu, N Meisgen, F Wei, T Brodin, P Jaks, V Kasper, M Shimokawa, T Harada, M Heilborn, J Hedblad, M-A Hippe, A Grandér, D Homey, B Zaphiropoulos, P G Arsenian-Henriksson, M Ståhle, M Pivarcsi, A MicroRNA-203 functions as a tumor suppressor in basal cell carcinoma |
title | MicroRNA-203 functions as a tumor suppressor in basal cell carcinoma |
title_full | MicroRNA-203 functions as a tumor suppressor in basal cell carcinoma |
title_fullStr | MicroRNA-203 functions as a tumor suppressor in basal cell carcinoma |
title_full_unstemmed | MicroRNA-203 functions as a tumor suppressor in basal cell carcinoma |
title_short | MicroRNA-203 functions as a tumor suppressor in basal cell carcinoma |
title_sort | microrna-203 functions as a tumor suppressor in basal cell carcinoma |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3412636/ https://www.ncbi.nlm.nih.gov/pubmed/23552555 http://dx.doi.org/10.1038/oncsis.2012.3 |
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