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Clinical implications of insulin-like growth factor 1 system in early-stage cervical cancer
This study was aimed to identify the expression and the correlation of insulin-like growth factor-1 (IGF-1) system and their prognostic impacts in cervical cancer. Seventy-two patients with early-stage cervical cancer were eligible. We obtained the serum levels of total IGF-1 and IGF binding protein...
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2567063/ https://www.ncbi.nlm.nih.gov/pubmed/18781172 http://dx.doi.org/10.1038/sj.bjc.6604661 |
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author | Huang, Y-F Shen, M-R Hsu, K-F Cheng, Y-M Chou, C-Y |
author_facet | Huang, Y-F Shen, M-R Hsu, K-F Cheng, Y-M Chou, C-Y |
author_sort | Huang, Y-F |
collection | PubMed |
description | This study was aimed to identify the expression and the correlation of insulin-like growth factor-1 (IGF-1) system and their prognostic impacts in cervical cancer. Seventy-two patients with early-stage cervical cancer were eligible. We obtained the serum levels of total IGF-1 and IGF binding protein-3 (IGFBP-3) by enzyme-linked immunosorbent assay and the expression of IGF-1 receptor (IGF-1R) in cancerous tissue by immuno-fluorescent (IF) stains. The 5-year recurrence-free and overall survival rates were significantly lower (P=0.003 and P=0.01, respectively) among patients with high-grade expression of tissue IGF-1R, compared with those with low-grade expression. After adjustment for other factors, preoperative serum total IGF-1 or IGFBP-3 levels failed to predict cancer death and recurrence. High-grade expression of IGF-1R and elevated preoperative squamous cell carcinoma antigen level were independent predictors of both death and recurrence, and combination of both factors could further help identify the subgroup of patients at higher death risk. The IF staining indicates the colocalisation of IGF-1 and IGF-1R in the cancerous tissues, whereas the IGF-1R expression is not correlated with circulating levels of IGF-1 or IGFBP-3. In early-stage cervical cancer, IGF-1 system may have a paracrine or autocrine function and the adverse impacts on prognosis by IGF-1R overexpression are implicated. |
format | Text |
id | pubmed-2567063 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-25670632009-10-07 Clinical implications of insulin-like growth factor 1 system in early-stage cervical cancer Huang, Y-F Shen, M-R Hsu, K-F Cheng, Y-M Chou, C-Y Br J Cancer Molecular Diagnostics This study was aimed to identify the expression and the correlation of insulin-like growth factor-1 (IGF-1) system and their prognostic impacts in cervical cancer. Seventy-two patients with early-stage cervical cancer were eligible. We obtained the serum levels of total IGF-1 and IGF binding protein-3 (IGFBP-3) by enzyme-linked immunosorbent assay and the expression of IGF-1 receptor (IGF-1R) in cancerous tissue by immuno-fluorescent (IF) stains. The 5-year recurrence-free and overall survival rates were significantly lower (P=0.003 and P=0.01, respectively) among patients with high-grade expression of tissue IGF-1R, compared with those with low-grade expression. After adjustment for other factors, preoperative serum total IGF-1 or IGFBP-3 levels failed to predict cancer death and recurrence. High-grade expression of IGF-1R and elevated preoperative squamous cell carcinoma antigen level were independent predictors of both death and recurrence, and combination of both factors could further help identify the subgroup of patients at higher death risk. The IF staining indicates the colocalisation of IGF-1 and IGF-1R in the cancerous tissues, whereas the IGF-1R expression is not correlated with circulating levels of IGF-1 or IGFBP-3. In early-stage cervical cancer, IGF-1 system may have a paracrine or autocrine function and the adverse impacts on prognosis by IGF-1R overexpression are implicated. Nature Publishing Group 2008-10-07 2008-09-09 /pmc/articles/PMC2567063/ /pubmed/18781172 http://dx.doi.org/10.1038/sj.bjc.6604661 Text en Copyright © 2008 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Molecular Diagnostics Huang, Y-F Shen, M-R Hsu, K-F Cheng, Y-M Chou, C-Y Clinical implications of insulin-like growth factor 1 system in early-stage cervical cancer |
title | Clinical implications of insulin-like growth factor 1 system in early-stage cervical cancer |
title_full | Clinical implications of insulin-like growth factor 1 system in early-stage cervical cancer |
title_fullStr | Clinical implications of insulin-like growth factor 1 system in early-stage cervical cancer |
title_full_unstemmed | Clinical implications of insulin-like growth factor 1 system in early-stage cervical cancer |
title_short | Clinical implications of insulin-like growth factor 1 system in early-stage cervical cancer |
title_sort | clinical implications of insulin-like growth factor 1 system in early-stage cervical cancer |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2567063/ https://www.ncbi.nlm.nih.gov/pubmed/18781172 http://dx.doi.org/10.1038/sj.bjc.6604661 |
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