Author:
Fontvieille Emma,His Mathilde,Biessy Carine,Navionis Anne-Sophie,Torres-Mejía Gabriela,Ángeles-Llerenas Angélica,Alvarado-Cabrero Isabel,Sánchez Gloria Inés,Navarro Edgar,Cortes Yorlany Rodas,Porras Carolina,Rodriguez Ana Cecilia,Garmendia Maria Luisa,Soto José Luis,Moyano Leonor,Porter Peggy L.,Lin Ming Gang,Guenthoer Jamie,Romieu Isabelle,Rinaldi Sabina,Tejeda Jenny,Lazcano María Felix,Franco Libia Zulema,Jaramillo Roberto,Angel Alberto,Ossa Carlos Andres,Arias William H.,Bedoya Gabriel,Cock-Rada Alicia,Echeverri Carolina,Herazo Fernando,Díaz-Yunez Israel,Hernández Angel,Cortes Bernal,Gonzalez Paula,Ocampo Rebecca,Guillen Diego,Loría Viviana,Vial Catalina,Diaz Lizette,Donato Elizabeth,Donn Thomas,Wirtala Kelly,Loucks Hailey,
Abstract
Abstract
Background
Breast cancer incidence is increasing rapidly in Latin America, with a higher proportion of cases among young women than in developed countries. Studies have linked inflammation to breast cancer development, but data is limited in premenopausal women, especially in Latin America.
Methods
We investigated the associations between serum biomarkers of chronic inflammation (interleukin (IL)-6, IL-8, IL-10, tumor necrosis factor-α (TNF-α), interferon-γ (IFN-γ), leptin, adiponectin) and risk of premenopausal breast cancer among 453 cases and 453 matched, population-based controls from Chile, Colombia, Costa Rica, and Mexico. Odds ratios (OR) were estimated using conditional logistic regression models. Analyses were stratified by size and hormonal receptor status of the tumors.
Results
IL-6 (ORper standard deviation (SD) = 1.33 (1.11–1.60)) and TNF-α (ORper SD = 1.32 (1.11–1.58)) were positively associated with breast cancer risk in fully adjusted models. Evidence of heterogeneity by estrogen receptor (ER) status was observed for IL-8 (P-homogeneity = 0.05), with a positive association in ER-negative tumors only. IL-8 (P-homogeneity = 0.06) and TNF-α (P-homogeneity = 0.003) were positively associated with risk in the largest tumors, while for leptin (P-homogeneity = 0.003) a positive association was observed for the smallest tumors only.
Conclusions
The results of this study support the implication of chronic inflammation in breast cancer risk in young women in Latin America. Largest studies of prospective design are needed to confirm these findings in premenopausal women.
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Genetics,Oncology