Associations between Genetically Predicted Blood Protein Biomarkers and Pancreatic Cancer Risk

Jingjing Zhu, Xiang Shu, Xingyi Guo, Duo Liu, Jiandong Bao, Roger L. Milne, Graham G. Giles, Chong Wu, Mengmeng Du, Emily White, Harvey A. Risch, Nuria Malats, Eric J. Duell, Phyllis J. Goodman, Donghui Li, Paige Bracci, Verena Katzke, Rachel E. Neale, Steven Gallinger, Stephen K. Van Den EedenAlan A. Arslan, Federico Canzian, Charles Kooperberg, Laura E. Beane Freeman, Ghislaine Scelo, Kala Visvanathan, Christopher A. Haiman, Loïc Le Marchand, Herbert Yu, Gloria M. Petersen, Rachael Stolzenberg-Solomon, Alison P. Klein, Qiuyin Cai, Jirong Long, Xiao Ou Shu, Wei Zheng, Lang Wu

Research output: Contribution to journalArticle

1 Scopus citations

Abstract

BACKGROUND: Pancreatic ductal adenocarcinoma (PDAC) is one of the most lethal malignancies, with few known risk factors and biomarkers. Several blood protein biomarkers have been linked to PDAC in previous studies, but these studies have assessed only a limited number of biomarkers, usually in small samples. In this study, we evaluated associations of circulating protein levels and PDAC risk using genetic instruments. METHODS: To identify novel circulating protein biomarkers of PDAC, we studied 8,280 cases and 6,728 controls of European descent from the Pancreatic Cancer Cohort Consortium and the Pancreatic Cancer Case-Control Consortium, using genetic instruments of protein quantitative trait loci. RESULTS: We observed associations between predicted concentrations of 38 proteins and PDAC risk at an FDR of < 0.05, including 23 of those proteins that showed an association even after Bonferroni correction. These include the protein encoded by ABO, which has been implicated as a potential target gene of PDAC risk variant. Eight of the identified proteins (LMA2L, TM11D, IP-10, ADH1B, STOM, TENC1, DOCK9, and CRBB2) were associated with PDAC risk after adjusting for previously reported PDAC risk variants (OR ranged from 0.79 to 1.52). Pathway enrichment analysis showed that the encoding genes for implicated proteins were significantly enriched in cancer-related pathways, such as STAT3 and IL15 production. CONCLUSIONS: We identified 38 candidates of protein biomarkers for PDAC risk. IMPACT: This study identifies novel protein biomarker candidates for PDAC, which if validated by additional studies, may contribute to the etiologic understanding of PDAC development.

ASJC Scopus subject areas

  • Epidemiology
  • Oncology

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