Abstract
Human genetic variation data are now publicly available on a large scale, from public and private discovery efforts. Datasets from the International Haplotype Map Consortium and Perlegen Sciences provide a level of knowledge about human genetic variation that is unprecedented. In combination with novel high-throughput genotyping technologies, these new resources will allow cancer prevention investigators to identify in a more precise way which genetic subsets of patients are likely to benefit most from chemoprevention and screening interventions.
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References and Recommended Reading
Lynch HT, Riley BD, Weissman SM, et al.: Hereditary nonpolyposis colorectal carcinoma (HNPCC) and HNPCClike families: problems in diagnosis, surveillance, and management. Cancer 2004, 100:53–64. Excellent review on the use of genetics to improve cancer screening and survival.
Wiesner GL, Daley D, Lewis S, et al.: A subset of familial colorectal neoplasia kindreds linked to chromosome 9q22.2-31. 2 Proc Natl Acad Sci U S A 2003, 100:12961–12965.
Hinds DA, Stuve LL, Nilsen GB, et al.: Whole-genome patterns of common DNA variation in three human populations. Science 2005, 307:1072–1079. An important original work that describes a state-of-the-art analysis of human genetic variation.
Collins FS: Genome research: the next generation. Cold Spring Harb Symp Quant Biol 2003, 68:49–54.
Crawford DC, Akey DT, Nickerson DA: The patterns of natural variation in human genes. Annu Rev Genomics Hum Genet 2005 May 19; [Epub ahead of print].
Crawford DC, Nickerson DA: Definition and clinical importance of haplotypes. Annu Rev Med 2005, 56:303–320. State-of-the-art review on SNPs and haplotypes.
Evans WE, McLeod HL: Pharmacogenomics: drug disposition, drug targets, and side effects. N Engl J Med 2003, 348:538–549. This review summarizes in an excellent manner the use of SNPs in pharmocogenentics/pharmacogenomics.
Weng WK, Levy R: Two immunoglobulin G fragment C receptor polymorphisms independently predict response to rituximab in patients with follicular lymphoma. J Clin Oncol 2003, 21:3940–3947.
Evans WE: Pharmacogenetics of thiopurine S-methyltransferase and thiopurine therapy. Ther Drug Monit 2004, 26:186–191.
Marsh S, McLeod HL: Pharmacogenetics of irinotecan toxicity. Pharmacogenomics 2004, 5:835–843.
Fukunaga AK, Marsh S, Murry DJ, et al.: Identification and analysis of single-nucleotide polymorphisms in the gemcitabine pharmacologic pathway. Pharmacogenomics 2004, J4:307–314.
McLeod HL, King CR, Marsh S: Application of pharmacogenomics in the individualization of chemotherapy for gastrointestinal malignancies. Clin Colorectal Cancer 2004, 4(Suppl 1):S43-S47.
Marsh S, McLeod HL: Cancer pharmacogenetics. Br J Cancer 2004, 90:8–11.
Keller JJ, Giardiello FM: Chemoprevention strategies using NSAIDs and COX-2 inhibitors. Cancer Biol Ther 2003, 2:S140-S149.
Annie Yu HJ, Lin KM, Ota DM, Lynch HT: Hereditary nonpolyposis colorectal cancer: preventive management. Cancer Treat Rev 2003, 29:461–470.
Graaf MR, Beiderbeck AB, Egberts AC, et al.: The risk of cancer in users of statins. J Clin Oncol 2004, 22:2388–2394. An excellent meta-analysis of the chemopreventive effects of statins in multiple cancer types.
Poynter JN, Gruber SB, Higgins PD, et al.: Statins and the risk of colorectal cancer. N Engl J Med 2005, 352:2184–2192.
Erlinger TP, Platz EA, Rifai N, Helzlsouer KJ: C-reactive protein and the risk of incident colorectal cancer. JAMA 2004, 291:585–590.
Lipkin SM, Rozek LS, Rennert G, et al.: The MLH1 D132H variant is associated with susceptibility to sporadic colorectal cancer. Nat Genet 2004, 36:694–699.
Siest G, Jeannesson E, Berrahmoune H, et al.: Pharmacogenomics and drug response in cardiovascular disorders. Pharmacogenomics 2004, 5:779–802.
Chasman DI, Posada D, Subrahmanyan L, et al.: Pharmacogenetic study of statin therapy and cholesterol reduction. JAMA 2004, 291:2821–2827.
de Groot E, Jukema JW, van Boven AJ, et al.: (1995) Effect of pravastatin on progression and regression of coronary atherosclerosis and vessel wall changes in carotid and femoral arteries: a report from the Regression Growth Evaluation Statin Study. Am J Cardiol 1995, 76:40C-46C.
Packham C, Robinson J, Morris J, et al.: Statin prescribing in Nottingham general practices: a cross-sectional study. J Public Health Med 1999, 21:60–64.
van Hout BA, Simoons ML: Cost-effectiveness of HMG coenzyme reductase inhibitors: whom to treat? Eur Heart J 2001, 22:751–761.
Puccetti L, Pasqui AL, Pastorelli M, et al.: Time-dependent effect of statins on platelet function in hypercholesterolaemia. Eur J Clin Invest 2002, 32:901–908.
Ozaki K, Ohnishi Y, Iida A, et al.: Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction. Nat Genet 2002, 32:650–654.
Undevia SD, Gomez-Abuin G, Ratain MJ: Pharmacokinetic variability of anticancer agents. Nat Rev Cancer 2005, 5:447–458.
Sklar P: Principles of haplotype mapping and potential applications to attention-deficit/hyperactivity disorder. Biol Psychiatry 2005, 57:1357–1366.
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Velasquez, J.L., Lipkin, S.M. What are SNPs and haplotypes and how will they help us manage the prevention of adult cancer?. Curr Oncol Rep 7, 475–479 (2005). https://doi.org/10.1007/s11912-005-0013-1
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DOI: https://doi.org/10.1007/s11912-005-0013-1