MiR-339-5p regulates the growth, colony formation and metastasis of colorectal cancer cells by targeting PRL-1.

MicroRNAs (miRNAs) have been suggested to play a vital role in regulate tumor progression and invasion. However, the expression of miR-339-5p in colorectal cancer and its effects are not known. Here, we report that miR-339-5p is a tumor suppressor by regulating expression of PRL-1. In this study, we...

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Autores principales: Chang Zhou, Guobing Liu, Lijing Wang, Yanxia Lu, Li Yuan, Lin Zheng, Fang Chen, Fanli Peng, Xuenong Li
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Publicado: Public Library of Science (PLoS) 2013
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Acceso en línea:https://doaj.org/article/a6cef5073086479a827f3e175e548a6b
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spelling oai:doaj.org-article:a6cef5073086479a827f3e175e548a6b2021-11-18T07:45:32ZMiR-339-5p regulates the growth, colony formation and metastasis of colorectal cancer cells by targeting PRL-1.1932-620310.1371/journal.pone.0063142https://doaj.org/article/a6cef5073086479a827f3e175e548a6b2013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23696794/?tool=EBIhttps://doaj.org/toc/1932-6203MicroRNAs (miRNAs) have been suggested to play a vital role in regulate tumor progression and invasion. However, the expression of miR-339-5p in colorectal cancer and its effects are not known. Here, we report that miR-339-5p is a tumor suppressor by regulating expression of PRL-1. In this study, we showed that downregulated miR-339-5p levels in colorectal cancer tissues and highly invasive CRC cell lines. Furthermore, enhancing the expression of miR-339-5p inhibited CRC cell growth, migration and invasion in vitro and suppressed tumor growth in vivo. We then screened and identified a novel miR-339-5p target, phosphatases of regenerating liver-1 1 (PRL-1), and it was further confirmed by luciferase assay. Overexpression of miR-339-5p would also reduce the expression of PRL-1 mRNA and protein. The reduced PRL-1 expression was associated with low expression of phosphorylated-extracellular signal-regulated kinase1/2 (p-ERK1/2). Conversely, reduction of miR-339-5p by inhibitors in cells stimulated these phenotypes. In conclusion, our results demonstrate that miR-339-5p functions as a tumor suppressor and plays a role in inhibiting growth and metastasis of CRC cells through targeting PRL-1 and regulating p-ERK1/2 .These findings suggest that miR-339-5p may be useful as a new potential therapeutic target for CRC.Chang ZhouGuobing LiuLijing WangYanxia LuLi YuanLin ZhengFang ChenFanli PengXuenong LiPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 8, Iss 5, p e63142 (2013)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Chang Zhou
Guobing Liu
Lijing Wang
Yanxia Lu
Li Yuan
Lin Zheng
Fang Chen
Fanli Peng
Xuenong Li
MiR-339-5p regulates the growth, colony formation and metastasis of colorectal cancer cells by targeting PRL-1.
description MicroRNAs (miRNAs) have been suggested to play a vital role in regulate tumor progression and invasion. However, the expression of miR-339-5p in colorectal cancer and its effects are not known. Here, we report that miR-339-5p is a tumor suppressor by regulating expression of PRL-1. In this study, we showed that downregulated miR-339-5p levels in colorectal cancer tissues and highly invasive CRC cell lines. Furthermore, enhancing the expression of miR-339-5p inhibited CRC cell growth, migration and invasion in vitro and suppressed tumor growth in vivo. We then screened and identified a novel miR-339-5p target, phosphatases of regenerating liver-1 1 (PRL-1), and it was further confirmed by luciferase assay. Overexpression of miR-339-5p would also reduce the expression of PRL-1 mRNA and protein. The reduced PRL-1 expression was associated with low expression of phosphorylated-extracellular signal-regulated kinase1/2 (p-ERK1/2). Conversely, reduction of miR-339-5p by inhibitors in cells stimulated these phenotypes. In conclusion, our results demonstrate that miR-339-5p functions as a tumor suppressor and plays a role in inhibiting growth and metastasis of CRC cells through targeting PRL-1 and regulating p-ERK1/2 .These findings suggest that miR-339-5p may be useful as a new potential therapeutic target for CRC.
format article
author Chang Zhou
Guobing Liu
Lijing Wang
Yanxia Lu
Li Yuan
Lin Zheng
Fang Chen
Fanli Peng
Xuenong Li
author_facet Chang Zhou
Guobing Liu
Lijing Wang
Yanxia Lu
Li Yuan
Lin Zheng
Fang Chen
Fanli Peng
Xuenong Li
author_sort Chang Zhou
title MiR-339-5p regulates the growth, colony formation and metastasis of colorectal cancer cells by targeting PRL-1.
title_short MiR-339-5p regulates the growth, colony formation and metastasis of colorectal cancer cells by targeting PRL-1.
title_full MiR-339-5p regulates the growth, colony formation and metastasis of colorectal cancer cells by targeting PRL-1.
title_fullStr MiR-339-5p regulates the growth, colony formation and metastasis of colorectal cancer cells by targeting PRL-1.
title_full_unstemmed MiR-339-5p regulates the growth, colony formation and metastasis of colorectal cancer cells by targeting PRL-1.
title_sort mir-339-5p regulates the growth, colony formation and metastasis of colorectal cancer cells by targeting prl-1.
publisher Public Library of Science (PLoS)
publishDate 2013
url https://doaj.org/article/a6cef5073086479a827f3e175e548a6b
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