Title |
Potential of Dihydropyrimidine Dehydrogenase Genotypes in Personalizing 5-Fluorouracil Therapy Among Colorectal Cancer Patients
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Published in |
Therapeutic Drug Monitoring, October 2013
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DOI | 10.1097/ftd.0b013e318290acd2 |
Pubmed ID | |
Authors |
Lay Kek Teh, Sharina Hamzah, Hazwanie Hashim, Zakaria Bannur, Zainul Amiruddin Zakaria, Zakaria Hasbullani, John Kwong Siew Shia, Henry Fijeraid, Azmid Md Nor, Mohd Zailani, Prabu Ramasamy, Harris Ngow, Suneet Sood, Mohd Zaki Salleh |
Abstract |
Dihydropyrimidine dehydrogenase (DPD) is a pyrimidine catabolic enzyme involved in the initial and rate-limiting step of the catabolic pathway of toxic metabolites of 5-fluorouracil (5-FU). Several studies have reported that deficiency of DPD and polymorphisms of its gene are related to 5-FU toxicities and death. Association between serum concentration of 5-FU and its related toxicity has also been previously demonstrated. Hence, this study aims to understand the role of DPYD variants in serum level of 5-FU and the risk of developing toxicity to prevent adverse reactions and maximize therapy outcome for personalized medicine. |
X Demographics
Geographical breakdown
Country | Count | As % |
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United States | 1 | 100% |
Demographic breakdown
Type | Count | As % |
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Science communicators (journalists, bloggers, editors) | 1 | 100% |
Mendeley readers
Geographical breakdown
Country | Count | As % |
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Unknown | 68 | 100% |
Demographic breakdown
Readers by professional status | Count | As % |
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Student > Master | 14 | 21% |
Researcher | 9 | 13% |
Student > Bachelor | 6 | 9% |
Student > Ph. D. Student | 6 | 9% |
Other | 5 | 7% |
Other | 13 | 19% |
Unknown | 15 | 22% |
Readers by discipline | Count | As % |
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Medicine and Dentistry | 16 | 24% |
Pharmacology, Toxicology and Pharmaceutical Science | 12 | 18% |
Agricultural and Biological Sciences | 10 | 15% |
Biochemistry, Genetics and Molecular Biology | 7 | 10% |
Immunology and Microbiology | 3 | 4% |
Other | 3 | 4% |
Unknown | 17 | 25% |