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Let-7c inhibits migration and epithelial–mesenchymal transition in head and neck squamous cell carcinoma by targeting IGF1R and HMGA2

To elucidate the molecular mechanisms underlying the progression of head and neck squamous cell carcinoma (HNSCC), we investigated the function of let-7c as a tumor suppressor. Let-7c expression was significantly down-regulated in HNSCC tumor tissues and cell lines. In vitro and in vivo studies reve...

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Autores principales: Hou, Bo, Ishinaga, Hajime, Midorikawa, Kaoru, Nakamura, Satoshi, Hiraku, Yusuke, Oikawa, Shinji, Ma, Ning, Takeuchi, Kazuhiko, Murata, Mariko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5823619/
https://www.ncbi.nlm.nih.gov/pubmed/29507664
http://dx.doi.org/10.18632/oncotarget.23826
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author Hou, Bo
Ishinaga, Hajime
Midorikawa, Kaoru
Nakamura, Satoshi
Hiraku, Yusuke
Oikawa, Shinji
Ma, Ning
Takeuchi, Kazuhiko
Murata, Mariko
author_facet Hou, Bo
Ishinaga, Hajime
Midorikawa, Kaoru
Nakamura, Satoshi
Hiraku, Yusuke
Oikawa, Shinji
Ma, Ning
Takeuchi, Kazuhiko
Murata, Mariko
author_sort Hou, Bo
collection PubMed
description To elucidate the molecular mechanisms underlying the progression of head and neck squamous cell carcinoma (HNSCC), we investigated the function of let-7c as a tumor suppressor. Let-7c expression was significantly down-regulated in HNSCC tumor tissues and cell lines. In vitro and in vivo studies revealed that let-7c negatively regulated HNSCC proliferation, migration and epithelial–mesenchymal transition (EMT). To explore the underlying mechanisms that affect these molecular events achieved by let-7c, we predicted its target genes. We performed luciferase assay and confirmed that insulin-like growth factor 1 receptor (IGF1R) and high mobility group AT-hook 2 (HMGA2) were the direct targets of let-7c. Knocking down of IGF1R and HMGA2 inhibited HNSCC progression, including proliferation, migration and EMT in HNSCC cells. Re-expression of these genes overcame let-7c–mediated inhibition. Taken together, our finding suggests that let-7c inhibits HNSCC progression by targeting IGF1R and HMGA2 and might be a novel target for HNSCC treatment.
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spelling pubmed-58236192018-03-05 Let-7c inhibits migration and epithelial–mesenchymal transition in head and neck squamous cell carcinoma by targeting IGF1R and HMGA2 Hou, Bo Ishinaga, Hajime Midorikawa, Kaoru Nakamura, Satoshi Hiraku, Yusuke Oikawa, Shinji Ma, Ning Takeuchi, Kazuhiko Murata, Mariko Oncotarget Research Paper To elucidate the molecular mechanisms underlying the progression of head and neck squamous cell carcinoma (HNSCC), we investigated the function of let-7c as a tumor suppressor. Let-7c expression was significantly down-regulated in HNSCC tumor tissues and cell lines. In vitro and in vivo studies revealed that let-7c negatively regulated HNSCC proliferation, migration and epithelial–mesenchymal transition (EMT). To explore the underlying mechanisms that affect these molecular events achieved by let-7c, we predicted its target genes. We performed luciferase assay and confirmed that insulin-like growth factor 1 receptor (IGF1R) and high mobility group AT-hook 2 (HMGA2) were the direct targets of let-7c. Knocking down of IGF1R and HMGA2 inhibited HNSCC progression, including proliferation, migration and EMT in HNSCC cells. Re-expression of these genes overcame let-7c–mediated inhibition. Taken together, our finding suggests that let-7c inhibits HNSCC progression by targeting IGF1R and HMGA2 and might be a novel target for HNSCC treatment. Impact Journals LLC 2018-01-02 /pmc/articles/PMC5823619/ /pubmed/29507664 http://dx.doi.org/10.18632/oncotarget.23826 Text en Copyright: © 2018 Hou 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 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Hou, Bo
Ishinaga, Hajime
Midorikawa, Kaoru
Nakamura, Satoshi
Hiraku, Yusuke
Oikawa, Shinji
Ma, Ning
Takeuchi, Kazuhiko
Murata, Mariko
Let-7c inhibits migration and epithelial–mesenchymal transition in head and neck squamous cell carcinoma by targeting IGF1R and HMGA2
title Let-7c inhibits migration and epithelial–mesenchymal transition in head and neck squamous cell carcinoma by targeting IGF1R and HMGA2
title_full Let-7c inhibits migration and epithelial–mesenchymal transition in head and neck squamous cell carcinoma by targeting IGF1R and HMGA2
title_fullStr Let-7c inhibits migration and epithelial–mesenchymal transition in head and neck squamous cell carcinoma by targeting IGF1R and HMGA2
title_full_unstemmed Let-7c inhibits migration and epithelial–mesenchymal transition in head and neck squamous cell carcinoma by targeting IGF1R and HMGA2
title_short Let-7c inhibits migration and epithelial–mesenchymal transition in head and neck squamous cell carcinoma by targeting IGF1R and HMGA2
title_sort let-7c inhibits migration and epithelial–mesenchymal transition in head and neck squamous cell carcinoma by targeting igf1r and hmga2
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5823619/
https://www.ncbi.nlm.nih.gov/pubmed/29507664
http://dx.doi.org/10.18632/oncotarget.23826
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