Cancer pharmacogenetics
- PMID: 14710198
- PMCID: PMC2395337
- DOI: 10.1038/sj.bjc.6601487
Cancer pharmacogenetics
Abstract
The large number of active combination chemotherapy regimens for most cancers has led to the need for better information to guide the 'standard' treatment for each patient. In an attempt to individualise therapy, pharmacogenetics and pharmacogenomics (a polygenic approach to pharmacogenetic studies) encompass the search for answers to the hereditary basis for interindividual differences in drug response. This review will focus on the results of studies assessing the effects of polymorphisms in drug-metabolising enzymes and drug targets on the toxicity and response to commonly used chemotherapy drugs. In addition, the need for polygenic pharmacogenomic strategies to identify patients at risk for adverse drug reactions will be highlighted.
Figures

Similar articles
-
Cancer pharmacogenomics: current and future applications.Biochim Biophys Acta. 2003 Mar 17;1603(2):99-111. doi: 10.1016/s0304-419x(03)00003-9. Biochim Biophys Acta. 2003. PMID: 12618310 Review.
-
Genetic polymorphisms of drug-metabolising enzymes and drug transporters in the chemotherapeutic treatment of cancer.Clin Pharmacokinet. 2006;45(3):253-85. doi: 10.2165/00003088-200645030-00003. Clin Pharmacokinet. 2006. PMID: 16509759 Review.
-
Genetic determinants of cancer drug efficacy and toxicity: practical considerations and perspectives.Anticancer Drugs. 2005 Oct;16(9):923-33. doi: 10.1097/01.cad.0000180120.39278.c9. Anticancer Drugs. 2005. PMID: 16162969 Review.
-
Cancer pharmacogenomics: international trends.Int J Clin Oncol. 2005 Feb;10(1):5-13. doi: 10.1007/s10147-004-0467-4. Int J Clin Oncol. 2005. PMID: 15729594 Review.
-
Pharmacogenetics of anti-cancer drugs: State of the art and implementation - recommendations of the French National Network of Pharmacogenetics.Therapie. 2017 Apr;72(2):205-215. doi: 10.1016/j.therap.2017.01.005. Epub 2017 Jan 30. Therapie. 2017. PMID: 28262261 Review.
Cited by
-
Hyperactivation of p21-Activated Kinases in Human Cancer and Therapeutic Sensitivity.Biomedicines. 2023 Feb 5;11(2):462. doi: 10.3390/biomedicines11020462. Biomedicines. 2023. PMID: 36830998 Free PMC article. Review.
-
A functional polymorphism of SSBP1 gene predicts prognosis and response to chemotherapy in resected gastric cancer patients.Oncotarget. 2017 Dec 2;8(67):110861-110876. doi: 10.18632/oncotarget.22864. eCollection 2017 Dec 19. Oncotarget. 2017. PMID: 29340022 Free PMC article.
-
Delivered dose: a drug-centric phenotype for chemotherapy dose individualization.Pharm Res. 2009 Aug;26(8):1803-6. doi: 10.1007/s11095-009-9913-3. Epub 2009 Jun 3. Pharm Res. 2009. PMID: 19495942
-
Creating and evaluating genetic tests predictive of drug response.Nat Rev Drug Discov. 2008 Jul;7(7):568-74. doi: 10.1038/nrd2520. Epub 2008 Jun 20. Nat Rev Drug Discov. 2008. PMID: 18587383 Free PMC article. Review.
-
Utility of Pretreatment Bilirubin Level and UGT1A1 Polymorphisms in Multivariate Predictive Models of Neutropenia Associated with Irinotecan Treatment in Previously Untreated Patients with Colorectal Cancer.Arch Drug Inf. 2008 Dec;1(3):97-106. doi: 10.1111/j.1753-5174.2008.00014.x. Arch Drug Inf. 2008. PMID: 19639031 Free PMC article.
References
-
- Ando Y, Saka H, Asai G, Sugiura S, Shimokata K, Kamataki T (1998) UGT1A1 genotypes and glucuronidation of SN-38, the active metabolite of irinotecan. Ann Oncol 9: 845–847 - PubMed
-
- Collie-Duguid ES, Etienne MC, Milano G, McLeod HL (2000) Known variant DPYD alleles do not explain DPD deficiency in cancer patients. Pharmacogenetics 10: 217–223 - PubMed
-
- Evans WE, McLeod HL (2003) Pharmacogenomics – drug disposition, drug targets, and side effects. N Engl J Med 348: 538–549 - PubMed
-
- Freimuth RR, Ameyaw MA, Pritchard SC, Kwok PY, McLeod HL (2003) High-throughput genotyping methods for pharmacogenomic studies. Curr Pharmacogenom, In press
-
- Horie N, Aiba H, Oguro K, Hojo H, Takeishi K (1995) Functional analysis and DNA polymorphism of the tandemly repeated sequences in the 5′-terminal regulatory region of the human gene for thymidylate synthase. Cell Struct Funct 20: 191–197 - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources