Genetic variation in TNF and IL10 and risk of non-Hodgkin lymphoma: a report from the InterLymph Consortium.

نویسندگان

  • Nathaniel Rothman
  • Christine F Skibola
  • Sophia S Wang
  • Gareth Morgan
  • Qing Lan
  • Martyn T Smith
  • John J Spinelli
  • Eleanor Willett
  • Silvia De Sanjose
  • Pierluigi Cocco
  • Sonja I Berndt
  • Paul Brennan
  • Angela Brooks-Wilson
  • Sholom Wacholder
  • Nikolaus Becker
  • Patricia Hartge
  • Tongzhang Zheng
  • Eve Roman
  • Elizabeth A Holly
  • Paolo Boffetta
  • Bruce Armstrong
  • Wendy Cozen
  • Martha Linet
  • F Xavier Bosch
  • Maria Grazia Ennas
  • Theodore R Holford
  • Richard P Gallagher
  • Sara Rollinson
  • Paige M Bracci
  • James R Cerhan
  • Denise Whitby
  • Patrick S Moore
  • Brian Leaderer
  • Agnes Lai
  • Charlotte Spink
  • Scott Davis
  • Ramon Bosch
  • Aldo Scarpa
  • Yawei Zhang
  • Richard K Severson
  • Meredith Yeager
  • Stephen Chanock
  • Alexandra Nieters
چکیده

BACKGROUND Common genetic variants in immune and inflammatory response genes can affect the risk of developing non-Hodgkin lymphoma. We aimed to test this hypothesis using previously unpublished data from eight European, Canadian, and US case-control studies of the International Lymphoma Epidemiology Consortium (InterLymph). METHODS We selected 12 single-nucleotide polymorphisms for analysis, on the basis of previous functional or association data, in nine genes that have important roles in lymphoid development, Th1/Th2 balance, and proinflammatory or anti-inflammatory pathways (IL1A, IL1RN, IL1B, IL2, IL6, IL10, TNF, LTA, and CARD15). Genotype data for one or more single-nucleotide polymorphisms were available for 3586 cases of non-Hodgkin lymphoma and for 4018 controls, and were assessed in a pooled analysis by use of a random-effects logistic regression model. FINDINGS The tumour necrosis factor (TNF) -308G-->A polymorphism was associated with increased risk of non-Hodgkin lymphoma (p for trend=0.005), particularly for diffuse large B-cell lymphoma, the main histological subtype (odds ratio 1.29 [95% CI 1.10-1.51] for GA and 1.65 [1.16-2.34] for AA, p for trend <0.0001), but not for follicular lymphoma. The interleukin 10 (IL10) -3575T-->A polymorphism was also associated with increased risk of non-Hodgkin lymphoma (p for trend=0.02), again particularly for diffuse large B-cell lymphoma (p for trend=0.006). For individuals homozygous for the TNF -308A allele and carrying at least one IL10 -3575A allele, risk of diffuse large B-cell lymphoma doubled (2.13 [1.37-3.32], p=0.00083). INTERPRETATION Common polymorphisms in TNF and IL10, key cytokines for the inflammatory response and Th1/Th2 balance, could be susceptibility loci for non-Hodgkin lymphoma. Moreover, our results underscore the importance of consortia for investigating the genetic basis of chronic diseases like cancer.

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عنوان ژورنال:
  • The Lancet. Oncology

دوره 7 1  شماره 

صفحات  -

تاریخ انتشار 2006