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URG11 Regulates Prostate Cancer Cell Proliferation, Migration, and Invasion
Upregulated gene 11 (URG11), a new gene upregulated by hepatitis B virus X protein, is involved in the development and progression of several tumors, including liver, stomach, lung, and colon cancers. However, the role of URG11 in prostate cancer remains yet to be elucidated. By determined expressio...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000846/ https://www.ncbi.nlm.nih.gov/pubmed/29955600 http://dx.doi.org/10.1155/2018/4060728 |
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author | Pan, Bin Ye, Yunlin Liu, Haiping Zhen, Jianli Zhou, Hongmei Li, Yutong Qu, Lijun Wu, Youke Zeng, Chuanrong Zhong, Weifeng |
author_facet | Pan, Bin Ye, Yunlin Liu, Haiping Zhen, Jianli Zhou, Hongmei Li, Yutong Qu, Lijun Wu, Youke Zeng, Chuanrong Zhong, Weifeng |
author_sort | Pan, Bin |
collection | PubMed |
description | Upregulated gene 11 (URG11), a new gene upregulated by hepatitis B virus X protein, is involved in the development and progression of several tumors, including liver, stomach, lung, and colon cancers. However, the role of URG11 in prostate cancer remains yet to be elucidated. By determined expression in human prostate cancer tissues, URG11 was found significantly upregulated and positively correlated with the severity of prostate cancer, compared with that in benign prostatic hyperplasia tissues. Further, the mRNA and protein levels of URG11 were significantly upregulated in human prostate cancer cell lines (DU145, PC3, and LNCaP), compared with human prostate epithelial cell line (RWPE-1). Moreover, by the application of siRNA against URG11, the proliferation, migration, and invasion of prostate cancer cells were markedly inhibited. Genetic knockdown of URG11 also induced cell cycle arrest at G1/S phase, induced apoptosis, and decreased the expression level of β-catenin in prostate cancer cells. Overexpression of URG11 promoted the expression of β-catenin, the growth, the migration, and invasion ability of prostate cancer cells. Taken together, this study reveals that URG11 is critical for the proliferation, migration, and invasion in prostate cancer cells, providing the evidence of URG11 to be a novel potential therapeutic target of prostate cancer. |
format | Online Article Text |
id | pubmed-6000846 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-60008462018-06-28 URG11 Regulates Prostate Cancer Cell Proliferation, Migration, and Invasion Pan, Bin Ye, Yunlin Liu, Haiping Zhen, Jianli Zhou, Hongmei Li, Yutong Qu, Lijun Wu, Youke Zeng, Chuanrong Zhong, Weifeng Biomed Res Int Research Article Upregulated gene 11 (URG11), a new gene upregulated by hepatitis B virus X protein, is involved in the development and progression of several tumors, including liver, stomach, lung, and colon cancers. However, the role of URG11 in prostate cancer remains yet to be elucidated. By determined expression in human prostate cancer tissues, URG11 was found significantly upregulated and positively correlated with the severity of prostate cancer, compared with that in benign prostatic hyperplasia tissues. Further, the mRNA and protein levels of URG11 were significantly upregulated in human prostate cancer cell lines (DU145, PC3, and LNCaP), compared with human prostate epithelial cell line (RWPE-1). Moreover, by the application of siRNA against URG11, the proliferation, migration, and invasion of prostate cancer cells were markedly inhibited. Genetic knockdown of URG11 also induced cell cycle arrest at G1/S phase, induced apoptosis, and decreased the expression level of β-catenin in prostate cancer cells. Overexpression of URG11 promoted the expression of β-catenin, the growth, the migration, and invasion ability of prostate cancer cells. Taken together, this study reveals that URG11 is critical for the proliferation, migration, and invasion in prostate cancer cells, providing the evidence of URG11 to be a novel potential therapeutic target of prostate cancer. Hindawi 2018-05-31 /pmc/articles/PMC6000846/ /pubmed/29955600 http://dx.doi.org/10.1155/2018/4060728 Text en Copyright © 2018 Bin Pan et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Pan, Bin Ye, Yunlin Liu, Haiping Zhen, Jianli Zhou, Hongmei Li, Yutong Qu, Lijun Wu, Youke Zeng, Chuanrong Zhong, Weifeng URG11 Regulates Prostate Cancer Cell Proliferation, Migration, and Invasion |
title | URG11 Regulates Prostate Cancer Cell Proliferation, Migration, and Invasion |
title_full | URG11 Regulates Prostate Cancer Cell Proliferation, Migration, and Invasion |
title_fullStr | URG11 Regulates Prostate Cancer Cell Proliferation, Migration, and Invasion |
title_full_unstemmed | URG11 Regulates Prostate Cancer Cell Proliferation, Migration, and Invasion |
title_short | URG11 Regulates Prostate Cancer Cell Proliferation, Migration, and Invasion |
title_sort | urg11 regulates prostate cancer cell proliferation, migration, and invasion |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000846/ https://www.ncbi.nlm.nih.gov/pubmed/29955600 http://dx.doi.org/10.1155/2018/4060728 |
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