A Prospective Study of XRCC1 Haplotypes and Their Interaction with Plasma Carotenoids on Breast Cancer Risk

Jiali Han, Susan E. Hankinson, Immaculata De Vivo, Donna Spiegelman, Rulla M. Tamimi, Harvey W. Mohrenweiser, Graham A. Colditz, David J. Hunter

Research output: Contribution to journalArticle

76 Citations (Scopus)

Abstract

The XRCC1 protein is involved in the base excision repair pathway through interactions with other proteins. Polymorphisms in the XRCC1 gene may lead to variation in repair proficiency and confer inherited predisposition to cancer. We prospectively assessed the associations between polymorphisms and haplotypes in XRCC1 and breast cancer risk in a nested case-control study within the Nurses' Health Study (incident cases, n = 1004; controls, n = 1385). We further investigated gene-environment interactions between the XRCC1 variations and plasma carotenoids on breast cancer risk. We genotyped four haplotype-tagging single nucleotide polymorphisms (Arg194Trp, C26602T, Arg 399Gln, and Gln632Gln) in the XRCC1 gene. Five common haplotypes accounted for 99% of the chromosomes in the present study population of mostly Caucasian women. We observed a marginally significant reduction in the risk of breast cancer among 194Trp carriers. As compared with nocarriers, women with at least one 194Trp allele had a multivariate odds ratio of 0.79 (95% of the confidence interval, 0.60-1.04). The inferred haplotype harboring the 194Trp allele was more common in controls than in cases (6.6 versus 5.3%, P = 0.07). We observed that the Arg 194Trp modified the inverse associations of plasma α-carotene level (P, ordinal test for interaction = 0.02) and plasma β-carotene level (P, ordinal test for interaction = 0.003) with breast cancer risk. No suggestion of an interaction was observed between the Arg 194Trp and cigarette smoking. Our results suggest an inverse association between XRCC1 194Trp allele and breast cancer risk. The findings of the effect modification of the Arg 194Trp on the relations of plasma α- and β-carotene levels with breast cancer risk suggest a potential protective effect of carotenoids in breast carcinogenesis by preventing oxidative DNA damage.

Original languageEnglish (US)
Pages (from-to)8536-8541
Number of pages6
JournalCancer Research
Volume63
Issue number23
StatePublished - Dec 1 2003
Externally publishedYes

Fingerprint

Carotenoids
Haplotypes
Prospective Studies
Breast Neoplasms
Alleles
Gene-Environment Interaction
Risk Reduction Behavior
DNA Repair
Genes
DNA Damage
Single Nucleotide Polymorphism
Case-Control Studies
Carcinogenesis
Proteins
Breast
Chromosomes
Smoking
Odds Ratio
Nurses
Confidence Intervals

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

Cite this

Han, J., Hankinson, S. E., De Vivo, I., Spiegelman, D., Tamimi, R. M., Mohrenweiser, H. W., ... Hunter, D. J. (2003). A Prospective Study of XRCC1 Haplotypes and Their Interaction with Plasma Carotenoids on Breast Cancer Risk. Cancer Research, 63(23), 8536-8541.

A Prospective Study of XRCC1 Haplotypes and Their Interaction with Plasma Carotenoids on Breast Cancer Risk. / Han, Jiali; Hankinson, Susan E.; De Vivo, Immaculata; Spiegelman, Donna; Tamimi, Rulla M.; Mohrenweiser, Harvey W.; Colditz, Graham A.; Hunter, David J.

In: Cancer Research, Vol. 63, No. 23, 01.12.2003, p. 8536-8541.

Research output: Contribution to journalArticle

Han, J, Hankinson, SE, De Vivo, I, Spiegelman, D, Tamimi, RM, Mohrenweiser, HW, Colditz, GA & Hunter, DJ 2003, 'A Prospective Study of XRCC1 Haplotypes and Their Interaction with Plasma Carotenoids on Breast Cancer Risk', Cancer Research, vol. 63, no. 23, pp. 8536-8541.
Han J, Hankinson SE, De Vivo I, Spiegelman D, Tamimi RM, Mohrenweiser HW et al. A Prospective Study of XRCC1 Haplotypes and Their Interaction with Plasma Carotenoids on Breast Cancer Risk. Cancer Research. 2003 Dec 1;63(23):8536-8541.
Han, Jiali ; Hankinson, Susan E. ; De Vivo, Immaculata ; Spiegelman, Donna ; Tamimi, Rulla M. ; Mohrenweiser, Harvey W. ; Colditz, Graham A. ; Hunter, David J. / A Prospective Study of XRCC1 Haplotypes and Their Interaction with Plasma Carotenoids on Breast Cancer Risk. In: Cancer Research. 2003 ; Vol. 63, No. 23. pp. 8536-8541.
@article{c48ca5056da54beb89b47adfe6f5bbf4,
title = "A Prospective Study of XRCC1 Haplotypes and Their Interaction with Plasma Carotenoids on Breast Cancer Risk",
abstract = "The XRCC1 protein is involved in the base excision repair pathway through interactions with other proteins. Polymorphisms in the XRCC1 gene may lead to variation in repair proficiency and confer inherited predisposition to cancer. We prospectively assessed the associations between polymorphisms and haplotypes in XRCC1 and breast cancer risk in a nested case-control study within the Nurses' Health Study (incident cases, n = 1004; controls, n = 1385). We further investigated gene-environment interactions between the XRCC1 variations and plasma carotenoids on breast cancer risk. We genotyped four haplotype-tagging single nucleotide polymorphisms (Arg194Trp, C26602T, Arg 399Gln, and Gln632Gln) in the XRCC1 gene. Five common haplotypes accounted for 99{\%} of the chromosomes in the present study population of mostly Caucasian women. We observed a marginally significant reduction in the risk of breast cancer among 194Trp carriers. As compared with nocarriers, women with at least one 194Trp allele had a multivariate odds ratio of 0.79 (95{\%} of the confidence interval, 0.60-1.04). The inferred haplotype harboring the 194Trp allele was more common in controls than in cases (6.6 versus 5.3{\%}, P = 0.07). We observed that the Arg 194Trp modified the inverse associations of plasma α-carotene level (P, ordinal test for interaction = 0.02) and plasma β-carotene level (P, ordinal test for interaction = 0.003) with breast cancer risk. No suggestion of an interaction was observed between the Arg 194Trp and cigarette smoking. Our results suggest an inverse association between XRCC1 194Trp allele and breast cancer risk. The findings of the effect modification of the Arg 194Trp on the relations of plasma α- and β-carotene levels with breast cancer risk suggest a potential protective effect of carotenoids in breast carcinogenesis by preventing oxidative DNA damage.",
author = "Jiali Han and Hankinson, {Susan E.} and {De Vivo}, Immaculata and Donna Spiegelman and Tamimi, {Rulla M.} and Mohrenweiser, {Harvey W.} and Colditz, {Graham A.} and Hunter, {David J.}",
year = "2003",
month = "12",
day = "1",
language = "English (US)",
volume = "63",
pages = "8536--8541",
journal = "Journal of Cancer Research",
issn = "0099-7013",
publisher = "American Association for Cancer Research Inc.",
number = "23",

}

TY - JOUR

T1 - A Prospective Study of XRCC1 Haplotypes and Their Interaction with Plasma Carotenoids on Breast Cancer Risk

AU - Han, Jiali

AU - Hankinson, Susan E.

AU - De Vivo, Immaculata

AU - Spiegelman, Donna

AU - Tamimi, Rulla M.

AU - Mohrenweiser, Harvey W.

AU - Colditz, Graham A.

AU - Hunter, David J.

PY - 2003/12/1

Y1 - 2003/12/1

N2 - The XRCC1 protein is involved in the base excision repair pathway through interactions with other proteins. Polymorphisms in the XRCC1 gene may lead to variation in repair proficiency and confer inherited predisposition to cancer. We prospectively assessed the associations between polymorphisms and haplotypes in XRCC1 and breast cancer risk in a nested case-control study within the Nurses' Health Study (incident cases, n = 1004; controls, n = 1385). We further investigated gene-environment interactions between the XRCC1 variations and plasma carotenoids on breast cancer risk. We genotyped four haplotype-tagging single nucleotide polymorphisms (Arg194Trp, C26602T, Arg 399Gln, and Gln632Gln) in the XRCC1 gene. Five common haplotypes accounted for 99% of the chromosomes in the present study population of mostly Caucasian women. We observed a marginally significant reduction in the risk of breast cancer among 194Trp carriers. As compared with nocarriers, women with at least one 194Trp allele had a multivariate odds ratio of 0.79 (95% of the confidence interval, 0.60-1.04). The inferred haplotype harboring the 194Trp allele was more common in controls than in cases (6.6 versus 5.3%, P = 0.07). We observed that the Arg 194Trp modified the inverse associations of plasma α-carotene level (P, ordinal test for interaction = 0.02) and plasma β-carotene level (P, ordinal test for interaction = 0.003) with breast cancer risk. No suggestion of an interaction was observed between the Arg 194Trp and cigarette smoking. Our results suggest an inverse association between XRCC1 194Trp allele and breast cancer risk. The findings of the effect modification of the Arg 194Trp on the relations of plasma α- and β-carotene levels with breast cancer risk suggest a potential protective effect of carotenoids in breast carcinogenesis by preventing oxidative DNA damage.

AB - The XRCC1 protein is involved in the base excision repair pathway through interactions with other proteins. Polymorphisms in the XRCC1 gene may lead to variation in repair proficiency and confer inherited predisposition to cancer. We prospectively assessed the associations between polymorphisms and haplotypes in XRCC1 and breast cancer risk in a nested case-control study within the Nurses' Health Study (incident cases, n = 1004; controls, n = 1385). We further investigated gene-environment interactions between the XRCC1 variations and plasma carotenoids on breast cancer risk. We genotyped four haplotype-tagging single nucleotide polymorphisms (Arg194Trp, C26602T, Arg 399Gln, and Gln632Gln) in the XRCC1 gene. Five common haplotypes accounted for 99% of the chromosomes in the present study population of mostly Caucasian women. We observed a marginally significant reduction in the risk of breast cancer among 194Trp carriers. As compared with nocarriers, women with at least one 194Trp allele had a multivariate odds ratio of 0.79 (95% of the confidence interval, 0.60-1.04). The inferred haplotype harboring the 194Trp allele was more common in controls than in cases (6.6 versus 5.3%, P = 0.07). We observed that the Arg 194Trp modified the inverse associations of plasma α-carotene level (P, ordinal test for interaction = 0.02) and plasma β-carotene level (P, ordinal test for interaction = 0.003) with breast cancer risk. No suggestion of an interaction was observed between the Arg 194Trp and cigarette smoking. Our results suggest an inverse association between XRCC1 194Trp allele and breast cancer risk. The findings of the effect modification of the Arg 194Trp on the relations of plasma α- and β-carotene levels with breast cancer risk suggest a potential protective effect of carotenoids in breast carcinogenesis by preventing oxidative DNA damage.

UR - http://www.scopus.com/inward/record.url?scp=0347626097&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0347626097&partnerID=8YFLogxK

M3 - Article

C2 - 14679022

AN - SCOPUS:0347626097

VL - 63

SP - 8536

EP - 8541

JO - Journal of Cancer Research

JF - Journal of Cancer Research

SN - 0099-7013

IS - 23

ER -