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Decreased expression of RASSF10 correlates with poor prognosis in patients with colorectal cancer
Ras association domain protein 10 (RASSF10) was reported to act as a prognostic indicator in various types of cancer and it was proved to be tumor suppressor gene in colorectal cancer (CRC). The purpose of this study was to evaluate the prognostic significance of RASSF10 in CRC. Quantitative real-ti...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5662333/ https://www.ncbi.nlm.nih.gov/pubmed/29049167 http://dx.doi.org/10.1097/MD.0000000000007011 |
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author | Ma, Junxun Zhang, Sujie Hu, Yi Li, Xiaoyan Yuan, Fang Sun, Danyang Wang, Lijie Zhang, Fan Chen, Guangying Cui, Pengfei |
author_facet | Ma, Junxun Zhang, Sujie Hu, Yi Li, Xiaoyan Yuan, Fang Sun, Danyang Wang, Lijie Zhang, Fan Chen, Guangying Cui, Pengfei |
author_sort | Ma, Junxun |
collection | PubMed |
description | Ras association domain protein 10 (RASSF10) was reported to act as a prognostic indicator in various types of cancer and it was proved to be tumor suppressor gene in colorectal cancer (CRC). The purpose of this study was to evaluate the prognostic significance of RASSF10 in CRC. Quantitative real-time polymerase chain reaction was used to detect the messenger RNA (mRNA) expression while enzyme-linked immunosorbent assay was taken to measure the protein expression of RASSF10 in tumor tissues and adjacent normal tissues from 102 patients with CRC. The relationship between RASSF10 expression level and clinical characteristics of CRC patients was analyzed by chi-squared test. In addition, the association between overall survival of CRC patients and RASSF10 expression was estimated by Kaplan–Meier analysis. Cox regression analysis was used to evaluate the prognostic value of RASSF10. The expression level of RASSF10 in tumor tissues was significantly lower than that in the normal tissues both at mRNA and protein levels. Moreover, the expression level was correlated with lymph-node-metastasis and tumor-node-metastasis stage. Kaplan–Meier analysis suggested that patients with high expression level of RASSF10 had a longer overall survival than those with low level (log-rank test, P < .001). Besides, RASSF10 might be a potential biomarker in the prognosis of CRC according to cox regression analysis. The down regulated of RASSF10 is found in CRC and it may be an ideal prognostic marker. |
format | Online Article Text |
id | pubmed-5662333 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-56623332017-11-21 Decreased expression of RASSF10 correlates with poor prognosis in patients with colorectal cancer Ma, Junxun Zhang, Sujie Hu, Yi Li, Xiaoyan Yuan, Fang Sun, Danyang Wang, Lijie Zhang, Fan Chen, Guangying Cui, Pengfei Medicine (Baltimore) 4500 Ras association domain protein 10 (RASSF10) was reported to act as a prognostic indicator in various types of cancer and it was proved to be tumor suppressor gene in colorectal cancer (CRC). The purpose of this study was to evaluate the prognostic significance of RASSF10 in CRC. Quantitative real-time polymerase chain reaction was used to detect the messenger RNA (mRNA) expression while enzyme-linked immunosorbent assay was taken to measure the protein expression of RASSF10 in tumor tissues and adjacent normal tissues from 102 patients with CRC. The relationship between RASSF10 expression level and clinical characteristics of CRC patients was analyzed by chi-squared test. In addition, the association between overall survival of CRC patients and RASSF10 expression was estimated by Kaplan–Meier analysis. Cox regression analysis was used to evaluate the prognostic value of RASSF10. The expression level of RASSF10 in tumor tissues was significantly lower than that in the normal tissues both at mRNA and protein levels. Moreover, the expression level was correlated with lymph-node-metastasis and tumor-node-metastasis stage. Kaplan–Meier analysis suggested that patients with high expression level of RASSF10 had a longer overall survival than those with low level (log-rank test, P < .001). Besides, RASSF10 might be a potential biomarker in the prognosis of CRC according to cox regression analysis. The down regulated of RASSF10 is found in CRC and it may be an ideal prognostic marker. Wolters Kluwer Health 2017-10-20 /pmc/articles/PMC5662333/ /pubmed/29049167 http://dx.doi.org/10.1097/MD.0000000000007011 Text en Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 |
spellingShingle | 4500 Ma, Junxun Zhang, Sujie Hu, Yi Li, Xiaoyan Yuan, Fang Sun, Danyang Wang, Lijie Zhang, Fan Chen, Guangying Cui, Pengfei Decreased expression of RASSF10 correlates with poor prognosis in patients with colorectal cancer |
title | Decreased expression of RASSF10 correlates with poor prognosis in patients with colorectal cancer |
title_full | Decreased expression of RASSF10 correlates with poor prognosis in patients with colorectal cancer |
title_fullStr | Decreased expression of RASSF10 correlates with poor prognosis in patients with colorectal cancer |
title_full_unstemmed | Decreased expression of RASSF10 correlates with poor prognosis in patients with colorectal cancer |
title_short | Decreased expression of RASSF10 correlates with poor prognosis in patients with colorectal cancer |
title_sort | decreased expression of rassf10 correlates with poor prognosis in patients with colorectal cancer |
topic | 4500 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5662333/ https://www.ncbi.nlm.nih.gov/pubmed/29049167 http://dx.doi.org/10.1097/MD.0000000000007011 |
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