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Cancer cachexia is associated with the IL10-1082 gene promoter polymorphism in patients with gastroesophageal malignancy

Cancer cachexia is associated with the IL10-1082 gene promoter polymorphism in patients with gastroesophageal malignancy
Cancer cachexia is associated with the IL10-1082 gene promoter polymorphism in patients with gastroesophageal malignancy
Background: The genetic predisposition of the host to local or systemic inflammation may contribute to the effect of cancer cachexia.

Objective: We investigated the relation between cytokine polymorphisms (IL1B -511, IL6 -174, IL10 -1082, TNFA -308, and LTA +252) and markers of nutritional status among patients with gastroesophageal cancer to determine whether any such association was reflected by cytokine concentrations in the tumor or plasma compartments.

Design: Patients (n = 203) with a diagnosis of gastroesophageal cancer underwent nutritional assessment (body mass index, anthropometric measures, dysphagia scoring, and estimation of dietary intake). Single nucleotide polymorphism genotyping was performed by TaqMan allelic discrimination genotyping. Serum cytokine and C-reactive protein concentrations were determined by enzyme-linked immunosorbent assay. Tumor tissue cytokine protein concentrations (n = 56) were determined by using the Cytometric Bead Array System.

Results: IL10 GG and IL6 CC polymorphisms were associated with elevated serum C-reactive protein concentrations, and the IL6 CC genotype was also associated with elevated tumor tissue cytokine concentrations. At diagnosis, the IL10 GG, but not the IL6, genotype was linked with increased total weight loss: 4.9% for AA, 7.1% for AG, and 12.0% for GG (P = 0.007). Serum C-reactive protein concentrations correlated with increased weight loss (r = 0.24, P < 0.001). Compared with other genotypes, the IL10 GG genotype retained an independent association in determining the extent of weight loss on multivariate analysis (95% CI: 0.52, 3.43; P = 0.008). Possession of the GG allele was associated with a 2.3 times increased risk of developing cachexia (95% CI: 1.2, 4.3; P = 0.014).

Conclusions: These data suggest that the IL10 genotype of the host can influence the development of cachexia among patients with gastroesophageal malignancy.

0002-9165
1164-1172
Deans, D.A. Chris
8d0a48be-1f9b-4962-bf86-a76a5ecd8c8e
Tan, Benjamin H.L.
c129e2ce-9a5b-4579-84f2-6971d60bbd03
Ross, James A.
abc04621-4eac-461b-85fb-b773df953a60
Rose-Zerilli, Matthew J.
08b3afa4-dbc2-4c0d-a852-2a9f33431199
Wigmore, Stephen J.
d9d153bc-0d57-4764-903b-539c8fce5247
Howell, W. Martin
ecbb0dd6-f904-4da2-a05d-e542862531f8
Grimble, Robert F.
3100e4d2-8f29-4ca6-a95d-38a6a764865f
Fearon, Kenneth C.H.
021154b0-9dc2-4bf0-ade9-891e2fe9a8fc
Deans, D.A. Chris
8d0a48be-1f9b-4962-bf86-a76a5ecd8c8e
Tan, Benjamin H.L.
c129e2ce-9a5b-4579-84f2-6971d60bbd03
Ross, James A.
abc04621-4eac-461b-85fb-b773df953a60
Rose-Zerilli, Matthew J.
08b3afa4-dbc2-4c0d-a852-2a9f33431199
Wigmore, Stephen J.
d9d153bc-0d57-4764-903b-539c8fce5247
Howell, W. Martin
ecbb0dd6-f904-4da2-a05d-e542862531f8
Grimble, Robert F.
3100e4d2-8f29-4ca6-a95d-38a6a764865f
Fearon, Kenneth C.H.
021154b0-9dc2-4bf0-ade9-891e2fe9a8fc

Deans, D.A. Chris, Tan, Benjamin H.L., Ross, James A., Rose-Zerilli, Matthew J., Wigmore, Stephen J., Howell, W. Martin, Grimble, Robert F. and Fearon, Kenneth C.H. (2009) Cancer cachexia is associated with the IL10-1082 gene promoter polymorphism in patients with gastroesophageal malignancy. American Journal of Clinical Nutrition, 89 (4), 1164-1172. (doi:10.3945/ajcn.2008.27025).

Record type: Article

Abstract

Background: The genetic predisposition of the host to local or systemic inflammation may contribute to the effect of cancer cachexia.

Objective: We investigated the relation between cytokine polymorphisms (IL1B -511, IL6 -174, IL10 -1082, TNFA -308, and LTA +252) and markers of nutritional status among patients with gastroesophageal cancer to determine whether any such association was reflected by cytokine concentrations in the tumor or plasma compartments.

Design: Patients (n = 203) with a diagnosis of gastroesophageal cancer underwent nutritional assessment (body mass index, anthropometric measures, dysphagia scoring, and estimation of dietary intake). Single nucleotide polymorphism genotyping was performed by TaqMan allelic discrimination genotyping. Serum cytokine and C-reactive protein concentrations were determined by enzyme-linked immunosorbent assay. Tumor tissue cytokine protein concentrations (n = 56) were determined by using the Cytometric Bead Array System.

Results: IL10 GG and IL6 CC polymorphisms were associated with elevated serum C-reactive protein concentrations, and the IL6 CC genotype was also associated with elevated tumor tissue cytokine concentrations. At diagnosis, the IL10 GG, but not the IL6, genotype was linked with increased total weight loss: 4.9% for AA, 7.1% for AG, and 12.0% for GG (P = 0.007). Serum C-reactive protein concentrations correlated with increased weight loss (r = 0.24, P < 0.001). Compared with other genotypes, the IL10 GG genotype retained an independent association in determining the extent of weight loss on multivariate analysis (95% CI: 0.52, 3.43; P = 0.008). Possession of the GG allele was associated with a 2.3 times increased risk of developing cachexia (95% CI: 1.2, 4.3; P = 0.014).

Conclusions: These data suggest that the IL10 genotype of the host can influence the development of cachexia among patients with gastroesophageal malignancy.

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Published date: 2009

Identifiers

Local EPrints ID: 154569
URI: http://eprints.soton.ac.uk/id/eprint/154569
ISSN: 0002-9165
PURE UUID: 25ac9984-16f5-4213-8f8c-174dba0fa006
ORCID for Matthew J. Rose-Zerilli: ORCID iD orcid.org/0000-0002-1064-5350

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Date deposited: 25 May 2010 14:04
Last modified: 14 Mar 2024 02:56

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Contributors

Author: D.A. Chris Deans
Author: Benjamin H.L. Tan
Author: James A. Ross
Author: Stephen J. Wigmore
Author: W. Martin Howell
Author: Robert F. Grimble
Author: Kenneth C.H. Fearon

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