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Cancer Research 69, 3681, April 15, 2009. Published Online First April 7, 2009;
doi: 10.1158/0008-5472.CAN-09-0015
© 2009 American Association for Cancer Research

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Molecular Biology, Pathobiology, and Genetics

Genetic Mutations Associated with Cigarette Smoking in Pancreatic Cancer

Amanda Blackford1, Giovanni Parmigiani1,2,5, Thomas W. Kensler6, Christopher Wolfgang3, Siân Jones1, Xiaosong Zhang1, D. Willams Parsons1, Jimmy Cheng-Ho Lin1, Rebecca J. Leary1, James R. Eshleman1,2, Michael Goggins1,2,4, Elizabeth M. Jaffee1,2, Christine A. Iacobuzio-Donahue1,2, Anirban Maitra1,4, Alison Klein1,2,7, John L. Cameron3, Kelly Olino3, Richard Schulick3, Jordan Winter3, Bert Vogelstein1,2, Victor E. Velculescu1, Kenneth W. Kinzler1 and Ralph H. Hruban1,2

Departments of 1 Oncology, 2 Pathology, 3 Surgery, and 4 Medicine, The Sol Goldman Pancreatic Cancer Research Center, The Johns Hopkins Medical Institutions; Departments of 5 Biostatistics, 6 Environmental Health Sciences, and 7 Epidemiology, Bloomberg School of Public Heath, Baltimore, Maryland

Requests for reprints: Ralph H. Hruban, Department of Pathology, The Johns Hopkins Medical Institutions, Weinberg 2242, 401 North Broadway, Baltimore, MD 21231. Phone: 410-955-9132; Fax: 410-955-0115; E-mail: rhruban{at}jhmi.edu.

Key Words: Mutations • Pancreatic Cancer • Smoking

Cigarette smoking doubles the risk of pancreatic cancer, and smoking accounts for 20% to 25% of pancreatic cancers. The recent sequencing of the pancreatic cancer genome provides an unprecedented opportunity to identify mutational patterns associated with smoking. We previously sequenced >750 million bp DNA from 23,219 transcripts in 24 adenocarcinomas of the pancreas (discovery screen). In this previous study, the 39 genes that were mutated more than once in the discovery screen were sequenced in an additional 90 adenocarcinomas of the pancreas (validation screen). Here, we compared the somatic mutations in the cancers obtained from individuals who ever smoked cigarettes (n = 64) to the somatic mutations in the cancers obtained from individuals who never smoked cigarettes (n = 50). When adjusted for age and gender, analyses of the discovery screen revealed significantly more nonsynonymous mutations in the carcinomas obtained from ever smokers (mean, 53.1 mutations per tumor; SD, 27.9) than in the carcinomas obtained from never smokers (mean, 38.5; SD, 11.1; P = 0.04). The difference between smokers and nonsmokers was not driven by mutations in known driver genes in pancreatic cancer (KRAS, TP53, CDKN2A/p16, and SMAD4), but instead was predominantly observed in genes mutated at lower frequency. No differences were observed in mutations in carcinomas from the head versus tail of the gland. Pancreatic carcinomas from cigarette smokers harbor more mutations than do carcinomas from never smokers. The types and patterns of these mutations provide insight into the mechanisms by which cigarette smoking causes pancreatic cancer. [Cancer Res 2009;69(8):3681–8]




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L. Wang, K. A. Brune, K. Visvanathan, D. Laheru, J. Herman, C. Wolfgang, R. Schulick, J. L. Cameron, M. Goggins, R. H. Hruban, et al.
Elevated Cancer Mortality in the Relatives of Patients with Pancreatic Cancer
Cancer Epidemiol. Biomarkers Prev., November 1, 2009; 18(11): 2829 - 2834.
[Abstract] [Full Text] [PDF]




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Copyright © 2009 by the American Association for Cancer Research.