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The prognostic factors and multiple biomarkers in young patients with colorectal cancer
The incidence of colorectal cancer (CRC) in young patients (≤50 years of age) appears to be increasing. However, their clinicopathological characteristics and survival are controversial. Likewise, the biomarkers are unclear. We used the West China (2008-2013, China), Surveillance, Epidemiology, and...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4445043/ https://www.ncbi.nlm.nih.gov/pubmed/26013439 http://dx.doi.org/10.1038/srep10645 |
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author | Wang, Mo-Jin Ping, Jie Li, Yuan Adell, Gunnar Arbman, Gunnar Nodin, Bjorn Meng, Wen-Jian Zhang, Hong Yu, Yong-Yang Wang, Cun Yang, Lie Zhou, Zong-Guang Sun, Xiao-Feng |
author_facet | Wang, Mo-Jin Ping, Jie Li, Yuan Adell, Gunnar Arbman, Gunnar Nodin, Bjorn Meng, Wen-Jian Zhang, Hong Yu, Yong-Yang Wang, Cun Yang, Lie Zhou, Zong-Guang Sun, Xiao-Feng |
author_sort | Wang, Mo-Jin |
collection | PubMed |
description | The incidence of colorectal cancer (CRC) in young patients (≤50 years of age) appears to be increasing. However, their clinicopathological characteristics and survival are controversial. Likewise, the biomarkers are unclear. We used the West China (2008-2013, China), Surveillance, Epidemiology, and End Results program (1973-2011, United States) and Linköping Cancer (1972-2009, Sweden) databases to analyse clinicopathological characteristics, survival and multiple biomarkers of young CRC patients. A total of 509,934 CRC patients were included from the three databases. The young CRC patients tended to have more distal location tumours, fewer tumour numbers, later stage, more mucinous carcinoma and poorer differentiation. The cancer-specific survival (CSS) of young patients was significantly better. The PRL (HR = 12.341, 95% CI = 1.615-94.276, P = 0.010), RBM3 (HR = 0.093, 95% CI = 0.012-0.712, P = 0.018), Wrap53 (HR = 1.952, 95% CI = 0.452-6.342, P = 0.031), p53 (HR = 5.549, 95% CI = 1.176-26.178, P = 0.045) and DNA status (HR = 17.602, 95% CI = 2.551-121.448, P = 0.001) were associated with CSS of the young patients. In conclusion, this study suggests that young CRC patients present advanced tumours and more malignant pathological features, while they have a better prognosis. The PRL, RBM3, Wrap53, p53 and DNA status are potential prognostic biomarkers for the young CRC patients. |
format | Online Article Text |
id | pubmed-4445043 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-44450432015-06-01 The prognostic factors and multiple biomarkers in young patients with colorectal cancer Wang, Mo-Jin Ping, Jie Li, Yuan Adell, Gunnar Arbman, Gunnar Nodin, Bjorn Meng, Wen-Jian Zhang, Hong Yu, Yong-Yang Wang, Cun Yang, Lie Zhou, Zong-Guang Sun, Xiao-Feng Sci Rep Article The incidence of colorectal cancer (CRC) in young patients (≤50 years of age) appears to be increasing. However, their clinicopathological characteristics and survival are controversial. Likewise, the biomarkers are unclear. We used the West China (2008-2013, China), Surveillance, Epidemiology, and End Results program (1973-2011, United States) and Linköping Cancer (1972-2009, Sweden) databases to analyse clinicopathological characteristics, survival and multiple biomarkers of young CRC patients. A total of 509,934 CRC patients were included from the three databases. The young CRC patients tended to have more distal location tumours, fewer tumour numbers, later stage, more mucinous carcinoma and poorer differentiation. The cancer-specific survival (CSS) of young patients was significantly better. The PRL (HR = 12.341, 95% CI = 1.615-94.276, P = 0.010), RBM3 (HR = 0.093, 95% CI = 0.012-0.712, P = 0.018), Wrap53 (HR = 1.952, 95% CI = 0.452-6.342, P = 0.031), p53 (HR = 5.549, 95% CI = 1.176-26.178, P = 0.045) and DNA status (HR = 17.602, 95% CI = 2.551-121.448, P = 0.001) were associated with CSS of the young patients. In conclusion, this study suggests that young CRC patients present advanced tumours and more malignant pathological features, while they have a better prognosis. The PRL, RBM3, Wrap53, p53 and DNA status are potential prognostic biomarkers for the young CRC patients. Nature Publishing Group 2015-05-27 /pmc/articles/PMC4445043/ /pubmed/26013439 http://dx.doi.org/10.1038/srep10645 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Wang, Mo-Jin Ping, Jie Li, Yuan Adell, Gunnar Arbman, Gunnar Nodin, Bjorn Meng, Wen-Jian Zhang, Hong Yu, Yong-Yang Wang, Cun Yang, Lie Zhou, Zong-Guang Sun, Xiao-Feng The prognostic factors and multiple biomarkers in young patients with colorectal cancer |
title | The prognostic factors and multiple biomarkers in young patients with colorectal cancer |
title_full | The prognostic factors and multiple biomarkers in young patients with colorectal cancer |
title_fullStr | The prognostic factors and multiple biomarkers in young patients with colorectal cancer |
title_full_unstemmed | The prognostic factors and multiple biomarkers in young patients with colorectal cancer |
title_short | The prognostic factors and multiple biomarkers in young patients with colorectal cancer |
title_sort | prognostic factors and multiple biomarkers in young patients with colorectal cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4445043/ https://www.ncbi.nlm.nih.gov/pubmed/26013439 http://dx.doi.org/10.1038/srep10645 |
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