4.5 Article

Antibody Responses to Streptococcus Gallolyticus Subspecies Gallolyticus Proteins in a Large Prospective Colorectal Cancer Cohort Consortium

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CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION
卷 27, 期 10, 页码 1186-1194

出版社

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1055-9965.EPI-18-0249

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资金

  1. NCI [R01 CA190428]
  2. Southern Community Cohort Study [U01 CA202979]
  3. NYU Women's Health Study
  4. NHS/HPFS [U01 CA167552, UM1 CA186107, P01 CA087969, UM1 CA167552]
  5. PHS [R01 CA097193, R01 CA040360, R01 HL034595]
  6. MEC [U01 CA164973]
  7. NIH [R01 AI039657, R01 AI118932, P01 CA116087]
  8. Department of Veterans Affairs [BX000627]
  9. National Heart, Lung, and Blood Institute, NIH, U.S. Department of Health and Human Services [HHSN268201600018C, HHSN268201600001C, HHSN268201600002C, HHSN268201600003C, HHSN268201600004C]
  10. Joint Initiative for Innovation and Research of the German Helmholtz Association
  11. [R01 DK058587]
  12. [R01 CA077955]

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Background: Antibody responses to Streptococcus gallolyticus subspecies gallolyticus (SGG) proteins, especially pilus protein Gallo2178, have been consistently associated with colorectal cancer risk. Previous case-control studies and prospective studies with up to 8 years of follow-up, however, were unable to decipher the temporality of antibody responses to SGG in the context of the long-term multistep development of colorectal cancer. In this study, we analyzed a large U.S. colorectal cancer cohort consortium with follow-up beyond 10 years for antibody responses to SGG. Methods: We applied multiplex serology to measure antibody responses to 9 SGG proteins in participants of 10 prospective U.S. cohorts (CLUE, CPSII, HPFS, MEC, NHS, NYUWHS, PHS, PLCO, SCCS, and WHI) including 4,063 incident colorectal cancer cases and 4,063 matched controls. Conditional logistic regression was used to assess whether antibody responses to SGG were associated with colorectal cancer risk, overall and by time between blood draw and diagnosis. Results: Colorectal cancer risk was increased among those with antibody responses to Gallo2178, albeit not statistically significant [OR, 1.23; 95% confidence interval (CI), 0.99-1.52]. This association was stronger for cases diagnosed <10 years after blood draw (OR, 1.40; 95% CI, 1.09-1.79), but was not found among cases diagnosed >= 10 years after blood draw (OR, 0.79; 95% CI, 0.50-1.24). Conclusions: In a large cohort consortium, we reproduced the association of antibody responses to SGG Gallo2178 with colorectal cancer risk for individuals diagnosed within 10 years after blood draw. Impact: This timing-specific finding suggests that antibody responses to SGG are associated with increased colorectal cancer risk only after tumorigenesis has begun. (C) 2018 AACR.

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