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MicroRNA-135b Promotes Cancer Progression by Acting as a Downstream Effector of Oncogenic Pathways in Colon Cancer
MicroRNA deregulation is frequent in human colorectal cancers (CRCs), but little is known as to whether it represents a bystander event or actually drives tumor progression in vivo. We show that miR-135b overexpression is triggered in mice and humans by APC loss, PTEN/PI3K pathway deregulation, and...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3995091/ https://www.ncbi.nlm.nih.gov/pubmed/24735923 http://dx.doi.org/10.1016/j.ccr.2014.03.006 |
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author | Valeri, Nicola Braconi, Chiara Gasparini, Pierluigi Murgia, Claudio Lampis, Andrea Paulus-Hock, Viola Hart, Jonathan R. Ueno, Lynn Grivennikov, Sergei I. Lovat, Francesca Paone, Alessio Cascione, Luciano Sumani, Khlea M. Veronese, Angelo Fabbri, Muller Carasi, Stefania Alder, Hansjuerg Lanza, Giovanni Gafa’, Roberta Moyer, Mary P. Ridgway, Rachel A. Cordero, Julia Nuovo, Gerard J. Frankel, Wendy L. Rugge, Massimo Fassan, Matteo Groden, Joanna Vogt, Peter K. Karin, Michael Sansom, Owen J. Croce, Carlo M. |
author_facet | Valeri, Nicola Braconi, Chiara Gasparini, Pierluigi Murgia, Claudio Lampis, Andrea Paulus-Hock, Viola Hart, Jonathan R. Ueno, Lynn Grivennikov, Sergei I. Lovat, Francesca Paone, Alessio Cascione, Luciano Sumani, Khlea M. Veronese, Angelo Fabbri, Muller Carasi, Stefania Alder, Hansjuerg Lanza, Giovanni Gafa’, Roberta Moyer, Mary P. Ridgway, Rachel A. Cordero, Julia Nuovo, Gerard J. Frankel, Wendy L. Rugge, Massimo Fassan, Matteo Groden, Joanna Vogt, Peter K. Karin, Michael Sansom, Owen J. Croce, Carlo M. |
author_sort | Valeri, Nicola |
collection | PubMed |
description | MicroRNA deregulation is frequent in human colorectal cancers (CRCs), but little is known as to whether it represents a bystander event or actually drives tumor progression in vivo. We show that miR-135b overexpression is triggered in mice and humans by APC loss, PTEN/PI3K pathway deregulation, and SRC overexpression and promotes tumor transformation and progression. We show that miR-135b upregulation is common in sporadic and inflammatory bowel disease-associated human CRCs and correlates with tumor stage and poor clinical outcome. Inhibition of miR-135b in CRC mouse models reduces tumor growth by controlling genes involved in proliferation, invasion, and apoptosis. We identify miR-135b as a key downsteam effector of oncogenic pathways and a potential target for CRC treatment. |
format | Online Article Text |
id | pubmed-3995091 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-39950912014-04-24 MicroRNA-135b Promotes Cancer Progression by Acting as a Downstream Effector of Oncogenic Pathways in Colon Cancer Valeri, Nicola Braconi, Chiara Gasparini, Pierluigi Murgia, Claudio Lampis, Andrea Paulus-Hock, Viola Hart, Jonathan R. Ueno, Lynn Grivennikov, Sergei I. Lovat, Francesca Paone, Alessio Cascione, Luciano Sumani, Khlea M. Veronese, Angelo Fabbri, Muller Carasi, Stefania Alder, Hansjuerg Lanza, Giovanni Gafa’, Roberta Moyer, Mary P. Ridgway, Rachel A. Cordero, Julia Nuovo, Gerard J. Frankel, Wendy L. Rugge, Massimo Fassan, Matteo Groden, Joanna Vogt, Peter K. Karin, Michael Sansom, Owen J. Croce, Carlo M. Cancer Cell Article MicroRNA deregulation is frequent in human colorectal cancers (CRCs), but little is known as to whether it represents a bystander event or actually drives tumor progression in vivo. We show that miR-135b overexpression is triggered in mice and humans by APC loss, PTEN/PI3K pathway deregulation, and SRC overexpression and promotes tumor transformation and progression. We show that miR-135b upregulation is common in sporadic and inflammatory bowel disease-associated human CRCs and correlates with tumor stage and poor clinical outcome. Inhibition of miR-135b in CRC mouse models reduces tumor growth by controlling genes involved in proliferation, invasion, and apoptosis. We identify miR-135b as a key downsteam effector of oncogenic pathways and a potential target for CRC treatment. Cell Press 2014-04-14 /pmc/articles/PMC3995091/ /pubmed/24735923 http://dx.doi.org/10.1016/j.ccr.2014.03.006 Text en © 2014 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/). |
spellingShingle | Article Valeri, Nicola Braconi, Chiara Gasparini, Pierluigi Murgia, Claudio Lampis, Andrea Paulus-Hock, Viola Hart, Jonathan R. Ueno, Lynn Grivennikov, Sergei I. Lovat, Francesca Paone, Alessio Cascione, Luciano Sumani, Khlea M. Veronese, Angelo Fabbri, Muller Carasi, Stefania Alder, Hansjuerg Lanza, Giovanni Gafa’, Roberta Moyer, Mary P. Ridgway, Rachel A. Cordero, Julia Nuovo, Gerard J. Frankel, Wendy L. Rugge, Massimo Fassan, Matteo Groden, Joanna Vogt, Peter K. Karin, Michael Sansom, Owen J. Croce, Carlo M. MicroRNA-135b Promotes Cancer Progression by Acting as a Downstream Effector of Oncogenic Pathways in Colon Cancer |
title | MicroRNA-135b Promotes Cancer Progression by Acting as a Downstream Effector of Oncogenic Pathways in Colon Cancer |
title_full | MicroRNA-135b Promotes Cancer Progression by Acting as a Downstream Effector of Oncogenic Pathways in Colon Cancer |
title_fullStr | MicroRNA-135b Promotes Cancer Progression by Acting as a Downstream Effector of Oncogenic Pathways in Colon Cancer |
title_full_unstemmed | MicroRNA-135b Promotes Cancer Progression by Acting as a Downstream Effector of Oncogenic Pathways in Colon Cancer |
title_short | MicroRNA-135b Promotes Cancer Progression by Acting as a Downstream Effector of Oncogenic Pathways in Colon Cancer |
title_sort | microrna-135b promotes cancer progression by acting as a downstream effector of oncogenic pathways in colon cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3995091/ https://www.ncbi.nlm.nih.gov/pubmed/24735923 http://dx.doi.org/10.1016/j.ccr.2014.03.006 |
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