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No Association of Insulin-like Growth Factor Gene Polymorphisms with Survival in Patients with Colorectal Cancer

PURPOSE: Insulin-like growth factors (IGF) regulate a wide range of biological functions including cell proliferation, differentiation, and apoptosis through paracrine and autocrine mechanisms. Accordingly, the present study analyzed polymorphisms of IGF genes and their impact on the prognosis for p...

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Autores principales: Cho, Yoon Young, Kim, Jong Gwang, Chae, Yee Soo, Sohn, Sang Kyun, Kang, Byung Woog, Moon, Joon Ho, Jeon, Seong Woo, Park, Jun Seok, Park, Jin Young, Choi, Gyu Seog
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Cancer Association 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3192881/
https://www.ncbi.nlm.nih.gov/pubmed/22022297
http://dx.doi.org/10.4143/crt.2011.43.3.189
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author Cho, Yoon Young
Kim, Jong Gwang
Chae, Yee Soo
Sohn, Sang Kyun
Kang, Byung Woog
Moon, Joon Ho
Jeon, Seong Woo
Park, Jun Seok
Park, Jin Young
Choi, Gyu Seog
author_facet Cho, Yoon Young
Kim, Jong Gwang
Chae, Yee Soo
Sohn, Sang Kyun
Kang, Byung Woog
Moon, Joon Ho
Jeon, Seong Woo
Park, Jun Seok
Park, Jin Young
Choi, Gyu Seog
author_sort Cho, Yoon Young
collection PubMed
description PURPOSE: Insulin-like growth factors (IGF) regulate a wide range of biological functions including cell proliferation, differentiation, and apoptosis through paracrine and autocrine mechanisms. Accordingly, the present study analyzed polymorphisms of IGF genes and their impact on the prognosis for patients with colorectal cancer. MATERIALS AND METHODS: Four hundred and two consecutive patients with curatively resected colorectal adenocarcinoma were enrolled in the present study. The genomic DNA was extracted from fresh colorectal tissue and 8 polymorphisms of IGF genes determined using a real-time polymerase chain reaction genotyping assay. RESULTS: Pathologic stages after surgery were as follows: stage 0/I (n=85, 21.1%), stage II (n=147, 36.6%), stage III (n=145, 36.1%), and stage IV (n=25, 6.2%). Multivariate survival analysis including stage, age, site of disease, and carcinoembryonic antigen level showed that the progression-free survival for patients with the IGF2 +1280 GG genotype was slightly better than for the patients with the combined IGF2 +1280 AA and AG genotype (p=0.056), although there was no significant difference in the overall survival. However, the other polymorphisms were not associated with survival. CONCLUSION: None of the 8 IGF1 or IGF2 gene polymorphisms investigated in this study were found to be independent prognostic markers for Korean patients with surgically resected colorectal cancer.
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spelling pubmed-31928812011-10-21 No Association of Insulin-like Growth Factor Gene Polymorphisms with Survival in Patients with Colorectal Cancer Cho, Yoon Young Kim, Jong Gwang Chae, Yee Soo Sohn, Sang Kyun Kang, Byung Woog Moon, Joon Ho Jeon, Seong Woo Park, Jun Seok Park, Jin Young Choi, Gyu Seog Cancer Res Treat Original Article PURPOSE: Insulin-like growth factors (IGF) regulate a wide range of biological functions including cell proliferation, differentiation, and apoptosis through paracrine and autocrine mechanisms. Accordingly, the present study analyzed polymorphisms of IGF genes and their impact on the prognosis for patients with colorectal cancer. MATERIALS AND METHODS: Four hundred and two consecutive patients with curatively resected colorectal adenocarcinoma were enrolled in the present study. The genomic DNA was extracted from fresh colorectal tissue and 8 polymorphisms of IGF genes determined using a real-time polymerase chain reaction genotyping assay. RESULTS: Pathologic stages after surgery were as follows: stage 0/I (n=85, 21.1%), stage II (n=147, 36.6%), stage III (n=145, 36.1%), and stage IV (n=25, 6.2%). Multivariate survival analysis including stage, age, site of disease, and carcinoembryonic antigen level showed that the progression-free survival for patients with the IGF2 +1280 GG genotype was slightly better than for the patients with the combined IGF2 +1280 AA and AG genotype (p=0.056), although there was no significant difference in the overall survival. However, the other polymorphisms were not associated with survival. CONCLUSION: None of the 8 IGF1 or IGF2 gene polymorphisms investigated in this study were found to be independent prognostic markers for Korean patients with surgically resected colorectal cancer. Korean Cancer Association 2011-09 2011-09-30 /pmc/articles/PMC3192881/ /pubmed/22022297 http://dx.doi.org/10.4143/crt.2011.43.3.189 Text en Copyright © 2011 by the Korean Cancer Association http://creativecommons.org/licenses/by-nc/3.0 This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Cho, Yoon Young
Kim, Jong Gwang
Chae, Yee Soo
Sohn, Sang Kyun
Kang, Byung Woog
Moon, Joon Ho
Jeon, Seong Woo
Park, Jun Seok
Park, Jin Young
Choi, Gyu Seog
No Association of Insulin-like Growth Factor Gene Polymorphisms with Survival in Patients with Colorectal Cancer
title No Association of Insulin-like Growth Factor Gene Polymorphisms with Survival in Patients with Colorectal Cancer
title_full No Association of Insulin-like Growth Factor Gene Polymorphisms with Survival in Patients with Colorectal Cancer
title_fullStr No Association of Insulin-like Growth Factor Gene Polymorphisms with Survival in Patients with Colorectal Cancer
title_full_unstemmed No Association of Insulin-like Growth Factor Gene Polymorphisms with Survival in Patients with Colorectal Cancer
title_short No Association of Insulin-like Growth Factor Gene Polymorphisms with Survival in Patients with Colorectal Cancer
title_sort no association of insulin-like growth factor gene polymorphisms with survival in patients with colorectal cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3192881/
https://www.ncbi.nlm.nih.gov/pubmed/22022297
http://dx.doi.org/10.4143/crt.2011.43.3.189
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