Plasma insulin-like growth factor 1, insulin-like growth factor binding protein 3, and risk of colorectal cancer: a prospective study in northern Sweden

Background: Insulin-like growth factor 1 (IGF-1) has antiapoptotic and mitogenic effects on various cell types, and raised IGF-1 levels are increasingly being implicated as potential risk factors for cancer. Aims: To examine the relationship between IGF-1 and its major plasma binding protein, IGF bi...

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Published in:Gut
Main Authors: Palmqvist, R, Hallmans, G, Rinaldi, S, Biessy, C, Stenling, R, Riboli, E, Kaaks, R
Format: Text
Language:English
Published: BMJ Publishing Group Ltd 2002
Subjects:
Online Access:http://gut.bmj.com/cgi/content/short/50/5/642
https://doi.org/10.1136/gut.50.5.642
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spelling fthighwire:oai:open-archive.highwire.org:gutjnl:50/5/642 2023-05-15T17:44:27+02:00 Plasma insulin-like growth factor 1, insulin-like growth factor binding protein 3, and risk of colorectal cancer: a prospective study in northern Sweden Palmqvist, R Hallmans, G Rinaldi, S Biessy, C Stenling, R Riboli, E Kaaks, R 2002-05-01 00:00:00.0 text/html http://gut.bmj.com/cgi/content/short/50/5/642 https://doi.org/10.1136/gut.50.5.642 en eng BMJ Publishing Group Ltd http://gut.bmj.com/cgi/content/short/50/5/642 http://dx.doi.org/10.1136/gut.50.5.642 Copyright (C) 2002, BMJ Publishing Group Colorectal cancer TEXT 2002 fthighwire https://doi.org/10.1136/gut.50.5.642 2015-02-28T19:03:31Z Background: Insulin-like growth factor 1 (IGF-1) has antiapoptotic and mitogenic effects on various cell types, and raised IGF-1 levels are increasingly being implicated as potential risk factors for cancer. Aims: To examine the relationship between IGF-1 and its major plasma binding protein, IGF binding protein 3 (IGFBP-3), and the risk of colorectal cancer. Methods: We conducted a case-control study nested within the Northern Sweden Health and Disease Cohort. IGF-1 and IGFBP-3 were measured in prediagnostic plasma samples from 168 men and women who developed cancers of the colon (n=110) or rectum (n=58), and from 336 matched controls. Results: Conditional logistic regression analyses showed an increase in colon cancer risk with increasing levels of IGF-1 (odds ratios (ORs) 1.00, 1.89, 2.30, 2.66; p trend =0.03) and IGFBP-3 (ORs 1.00, 0.91, 1.80, 1.93; p trend =0.02). Rectal cancer risk was inversely related to levels of IGF-1 (ORs 1.00, 0.45, 0.33, 0.33; p trend =0.09) and IGFBP-3 (ORs 1.00, 0.75, 0.66, 0.49; p trend =0.21). Mutual adjustments between IGF-1 and IGFBP-3 did not materially alter these relationships. Conclusions: These results support earlier findings of increased risk of colon cancer in subjects with elevated plasma IGF-1. Our results however do not support the hypothesis that the risk of rectal cancer could also be directly related to IGF-1 levels. Text Northern Sweden HighWire Press (Stanford University) Gut 50 5 642 646
institution Open Polar
collection HighWire Press (Stanford University)
op_collection_id fthighwire
language English
topic Colorectal cancer
spellingShingle Colorectal cancer
Palmqvist, R
Hallmans, G
Rinaldi, S
Biessy, C
Stenling, R
Riboli, E
Kaaks, R
Plasma insulin-like growth factor 1, insulin-like growth factor binding protein 3, and risk of colorectal cancer: a prospective study in northern Sweden
topic_facet Colorectal cancer
description Background: Insulin-like growth factor 1 (IGF-1) has antiapoptotic and mitogenic effects on various cell types, and raised IGF-1 levels are increasingly being implicated as potential risk factors for cancer. Aims: To examine the relationship between IGF-1 and its major plasma binding protein, IGF binding protein 3 (IGFBP-3), and the risk of colorectal cancer. Methods: We conducted a case-control study nested within the Northern Sweden Health and Disease Cohort. IGF-1 and IGFBP-3 were measured in prediagnostic plasma samples from 168 men and women who developed cancers of the colon (n=110) or rectum (n=58), and from 336 matched controls. Results: Conditional logistic regression analyses showed an increase in colon cancer risk with increasing levels of IGF-1 (odds ratios (ORs) 1.00, 1.89, 2.30, 2.66; p trend =0.03) and IGFBP-3 (ORs 1.00, 0.91, 1.80, 1.93; p trend =0.02). Rectal cancer risk was inversely related to levels of IGF-1 (ORs 1.00, 0.45, 0.33, 0.33; p trend =0.09) and IGFBP-3 (ORs 1.00, 0.75, 0.66, 0.49; p trend =0.21). Mutual adjustments between IGF-1 and IGFBP-3 did not materially alter these relationships. Conclusions: These results support earlier findings of increased risk of colon cancer in subjects with elevated plasma IGF-1. Our results however do not support the hypothesis that the risk of rectal cancer could also be directly related to IGF-1 levels.
format Text
author Palmqvist, R
Hallmans, G
Rinaldi, S
Biessy, C
Stenling, R
Riboli, E
Kaaks, R
author_facet Palmqvist, R
Hallmans, G
Rinaldi, S
Biessy, C
Stenling, R
Riboli, E
Kaaks, R
author_sort Palmqvist, R
title Plasma insulin-like growth factor 1, insulin-like growth factor binding protein 3, and risk of colorectal cancer: a prospective study in northern Sweden
title_short Plasma insulin-like growth factor 1, insulin-like growth factor binding protein 3, and risk of colorectal cancer: a prospective study in northern Sweden
title_full Plasma insulin-like growth factor 1, insulin-like growth factor binding protein 3, and risk of colorectal cancer: a prospective study in northern Sweden
title_fullStr Plasma insulin-like growth factor 1, insulin-like growth factor binding protein 3, and risk of colorectal cancer: a prospective study in northern Sweden
title_full_unstemmed Plasma insulin-like growth factor 1, insulin-like growth factor binding protein 3, and risk of colorectal cancer: a prospective study in northern Sweden
title_sort plasma insulin-like growth factor 1, insulin-like growth factor binding protein 3, and risk of colorectal cancer: a prospective study in northern sweden
publisher BMJ Publishing Group Ltd
publishDate 2002
url http://gut.bmj.com/cgi/content/short/50/5/642
https://doi.org/10.1136/gut.50.5.642
genre Northern Sweden
genre_facet Northern Sweden
op_relation http://gut.bmj.com/cgi/content/short/50/5/642
http://dx.doi.org/10.1136/gut.50.5.642
op_rights Copyright (C) 2002, BMJ Publishing Group
op_doi https://doi.org/10.1136/gut.50.5.642
container_title Gut
container_volume 50
container_issue 5
container_start_page 642
op_container_end_page 646
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