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MicroRNA-497 inhibits tumor growth and increases chemosensitivity to 5-fluorouracil treatment by targeting KSR1
Colorectal cancer (CRC) is one of the leading cancer-related causes of death in the world. Recently, downregulation of microRNA-497 (miR-497) has been observed in CRC tissues. In this study, we found that miR-497 expression levels were downregulated in human CRC specimens compared to the adjacent no...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4823062/ https://www.ncbi.nlm.nih.gov/pubmed/26673620 http://dx.doi.org/10.18632/oncotarget.6545 |
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author | Wang, Lin Jiang, Cheng-fei Li, Dong-mei Ge, Xin Shi, Zhu-mei Li, Chong-yong Liu, Xue Yin, Yu Zhen, Linlin Liu, Ling-Zhi Jiang, Bing-Hua |
author_facet | Wang, Lin Jiang, Cheng-fei Li, Dong-mei Ge, Xin Shi, Zhu-mei Li, Chong-yong Liu, Xue Yin, Yu Zhen, Linlin Liu, Ling-Zhi Jiang, Bing-Hua |
author_sort | Wang, Lin |
collection | PubMed |
description | Colorectal cancer (CRC) is one of the leading cancer-related causes of death in the world. Recently, downregulation of microRNA-497 (miR-497) has been observed in CRC tissues. In this study, we found that miR-497 expression levels were downregulated in human CRC specimens compared to the adjacent normal tissues. MiR-497 expression levels were strongly correlated with clinical stages and lymph node metastases. Furthermore, kinase suppressor of ras 1 (KSR1), a known oncogene, was a direct target of miR-497, and KSR1 expression levels were inversely correlated with miR-497 expression levels in human CRC specimens. Overexpression of miR-497 inhibited cell proliferation, migration, invasion and increased chemosensitivity to 5-fluorouracil treatment, whereas forced expression of KSR1 had the opposite effect. Taken together, these results revealed that lower miR-497 levels in human CRC tissues induce KSR1 expression which is associated with CRC cancer occurrence, advanced stages, metastasis and chemoresistance. Lower miR-497 levels may be a potential biomarker for CRC advanced stages and treatment response. |
format | Online Article Text |
id | pubmed-4823062 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-48230622016-05-03 MicroRNA-497 inhibits tumor growth and increases chemosensitivity to 5-fluorouracil treatment by targeting KSR1 Wang, Lin Jiang, Cheng-fei Li, Dong-mei Ge, Xin Shi, Zhu-mei Li, Chong-yong Liu, Xue Yin, Yu Zhen, Linlin Liu, Ling-Zhi Jiang, Bing-Hua Oncotarget Research Paper Colorectal cancer (CRC) is one of the leading cancer-related causes of death in the world. Recently, downregulation of microRNA-497 (miR-497) has been observed in CRC tissues. In this study, we found that miR-497 expression levels were downregulated in human CRC specimens compared to the adjacent normal tissues. MiR-497 expression levels were strongly correlated with clinical stages and lymph node metastases. Furthermore, kinase suppressor of ras 1 (KSR1), a known oncogene, was a direct target of miR-497, and KSR1 expression levels were inversely correlated with miR-497 expression levels in human CRC specimens. Overexpression of miR-497 inhibited cell proliferation, migration, invasion and increased chemosensitivity to 5-fluorouracil treatment, whereas forced expression of KSR1 had the opposite effect. Taken together, these results revealed that lower miR-497 levels in human CRC tissues induce KSR1 expression which is associated with CRC cancer occurrence, advanced stages, metastasis and chemoresistance. Lower miR-497 levels may be a potential biomarker for CRC advanced stages and treatment response. Impact Journals LLC 2015-12-09 /pmc/articles/PMC4823062/ /pubmed/26673620 http://dx.doi.org/10.18632/oncotarget.6545 Text en Copyright: © 2016 Wang et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Wang, Lin Jiang, Cheng-fei Li, Dong-mei Ge, Xin Shi, Zhu-mei Li, Chong-yong Liu, Xue Yin, Yu Zhen, Linlin Liu, Ling-Zhi Jiang, Bing-Hua MicroRNA-497 inhibits tumor growth and increases chemosensitivity to 5-fluorouracil treatment by targeting KSR1 |
title | MicroRNA-497 inhibits tumor growth and increases chemosensitivity to 5-fluorouracil treatment by targeting KSR1 |
title_full | MicroRNA-497 inhibits tumor growth and increases chemosensitivity to 5-fluorouracil treatment by targeting KSR1 |
title_fullStr | MicroRNA-497 inhibits tumor growth and increases chemosensitivity to 5-fluorouracil treatment by targeting KSR1 |
title_full_unstemmed | MicroRNA-497 inhibits tumor growth and increases chemosensitivity to 5-fluorouracil treatment by targeting KSR1 |
title_short | MicroRNA-497 inhibits tumor growth and increases chemosensitivity to 5-fluorouracil treatment by targeting KSR1 |
title_sort | microrna-497 inhibits tumor growth and increases chemosensitivity to 5-fluorouracil treatment by targeting ksr1 |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4823062/ https://www.ncbi.nlm.nih.gov/pubmed/26673620 http://dx.doi.org/10.18632/oncotarget.6545 |
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