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miR-206/133b Cluster: A Weapon against Lung Cancer?

Lung cancer is a deadly disease that ends numerous lives around the world. MicroRNAs (miRNAs) are a group of non-coding RNAs involved in a variety of biological processes, such as cell growth, organ development, and tumorigenesis. The miR-206/133b cluster is located on the human chromosome 6p12.2, w...

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Autores principales: Pan, Jing-Yu, Sun, Cheng-Cao, Bi, Zhuo-Yue, Chen, Zhen-Long, Li, Shu-Jun, Li, Qing-Qun, Wang, Yu-Xuan, Bi, Yong-Yi, Li, De-Jia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5542379/
https://www.ncbi.nlm.nih.gov/pubmed/28918043
http://dx.doi.org/10.1016/j.omtn.2017.06.002
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author Pan, Jing-Yu
Sun, Cheng-Cao
Bi, Zhuo-Yue
Chen, Zhen-Long
Li, Shu-Jun
Li, Qing-Qun
Wang, Yu-Xuan
Bi, Yong-Yi
Li, De-Jia
author_facet Pan, Jing-Yu
Sun, Cheng-Cao
Bi, Zhuo-Yue
Chen, Zhen-Long
Li, Shu-Jun
Li, Qing-Qun
Wang, Yu-Xuan
Bi, Yong-Yi
Li, De-Jia
author_sort Pan, Jing-Yu
collection PubMed
description Lung cancer is a deadly disease that ends numerous lives around the world. MicroRNAs (miRNAs) are a group of non-coding RNAs involved in a variety of biological processes, such as cell growth, organ development, and tumorigenesis. The miR-206/133b cluster is located on the human chromosome 6p12.2, which is essential for growth and rebuilding of skeletal muscle. The miR-206/133b cluster has been verified to be dysregulated and plays a crucial role in lung cancer. miR-206 and miR-133b participate in lung tumor cell apoptosis, proliferation, migration, invasion, angiogenesis, drug resistance, and cancer treatment. The mechanisms are sophisticated, involving various target genes and molecular pathways, such as MET, EGFR, and the STAT3/HIF-1α/VEGF signal pathway. Hence, in this review, we summarize the role and potential mechanisms of the miR-206/133b cluster in lung cancer.
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spelling pubmed-55423792017-08-09 miR-206/133b Cluster: A Weapon against Lung Cancer? Pan, Jing-Yu Sun, Cheng-Cao Bi, Zhuo-Yue Chen, Zhen-Long Li, Shu-Jun Li, Qing-Qun Wang, Yu-Xuan Bi, Yong-Yi Li, De-Jia Mol Ther Nucleic Acids Review Lung cancer is a deadly disease that ends numerous lives around the world. MicroRNAs (miRNAs) are a group of non-coding RNAs involved in a variety of biological processes, such as cell growth, organ development, and tumorigenesis. The miR-206/133b cluster is located on the human chromosome 6p12.2, which is essential for growth and rebuilding of skeletal muscle. The miR-206/133b cluster has been verified to be dysregulated and plays a crucial role in lung cancer. miR-206 and miR-133b participate in lung tumor cell apoptosis, proliferation, migration, invasion, angiogenesis, drug resistance, and cancer treatment. The mechanisms are sophisticated, involving various target genes and molecular pathways, such as MET, EGFR, and the STAT3/HIF-1α/VEGF signal pathway. Hence, in this review, we summarize the role and potential mechanisms of the miR-206/133b cluster in lung cancer. American Society of Gene & Cell Therapy 2017-06-07 /pmc/articles/PMC5542379/ /pubmed/28918043 http://dx.doi.org/10.1016/j.omtn.2017.06.002 Text en © 2017 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review
Pan, Jing-Yu
Sun, Cheng-Cao
Bi, Zhuo-Yue
Chen, Zhen-Long
Li, Shu-Jun
Li, Qing-Qun
Wang, Yu-Xuan
Bi, Yong-Yi
Li, De-Jia
miR-206/133b Cluster: A Weapon against Lung Cancer?
title miR-206/133b Cluster: A Weapon against Lung Cancer?
title_full miR-206/133b Cluster: A Weapon against Lung Cancer?
title_fullStr miR-206/133b Cluster: A Weapon against Lung Cancer?
title_full_unstemmed miR-206/133b Cluster: A Weapon against Lung Cancer?
title_short miR-206/133b Cluster: A Weapon against Lung Cancer?
title_sort mir-206/133b cluster: a weapon against lung cancer?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5542379/
https://www.ncbi.nlm.nih.gov/pubmed/28918043
http://dx.doi.org/10.1016/j.omtn.2017.06.002
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