Abstract

Objective: Dihydropyrimidine dehydrogenase (DPD), an enzyme translated by DPD gene (DPYD), has a critical role in the metabolism of 5-fluorouracil (5FU). In this study we aimed to investigate the frequency of the IVS14+1 G>A, 2194G>A, 2846 A>T mutations in the DPYD gene in colorectal cancer patients in north of Iran and their association with side effects of 5FU.Methods: Venous blood samples of 89 colorectal cancer patients were drawn. After the DNA extraction from nuclear cells, a polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method was used to detect the frequency of the IVS14+1 G>A and 2846 A>T mutations. Tetra-Primer ARMS PCR optimization method was used to detect the 2194 G>A mutation. Side effects were classified according to CTCAE (common terminology criteria for adverse events V. 4) and the association between different polymorphisms and side effects were evaluated.Results: Of 89 colorectal patients, the frequency of IVS14+1 G>A and 2846 A>T polymorphism was 4 (5.1%) and 1 (1.1%), respectively. The 2194 G>A polymorphism was not detected. All 4 patients were heterozygous for IVS14+1 G>A mutation, whereas the only patient with 2846 A>T polymorphism was homozygous. Some adverse effects of 5FU including diarrhea, vomiting, mucositis and stomatitis were more frequent in patients with IVS14+1 G>A polymorphism.Conclusion: The prevalence of IVS14+1 G>A mutation in our patients were relatively high and was associated with a higher occurrence of 5FU-associated toxicities.

Highlights

  • Colorectal cancer (CRC) is one of the most important causes of cancer-related mortalities worldwide [1]

  • Considering lack of data regarding the frequency of Dihydropyrimidine dehydrogenase (DPYD) polymorphism in our colorectal patients and its association with 5FU-associated toxicity, the aim of this study was to determine three allelic variants of DPYD (IVS14+1 G>A, 2846 A>T and 2194 G>A mutation) and their association with Adverse drug reactions (ADRs) of chemotherapy regimen containing 5FU in a group of colorectal cancer patients in North of Iran

  • The frequency of three DPYD gene polymorphisms including IVS14+1 G>A, 2846 A>T and 2194 G>A and their association with 5FU-associated toxicity were determined in a group of colorectal cancer patients in North of Iran

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Summary

Introduction

Colorectal cancer (CRC) is one of the most important causes of cancer-related mortalities worldwide [1]. Lack of DPD gene is a risk factor for developing severe toxicity in treatment by 5-FU drug. Carriers of some alleles such as IVS14+1 G>A, 2846 A>T and 2194 G>A mutation have significantly reduced DPD enzyme levels, resulting in less clearance of 5-FU and such are more likely to develop adverse toxicity following treatment with 5-FU drugs. Some studies have found that 27%-57% of cancer patients with IVS14+1G > A mutation suffered from severe 5-FU-associated toxicity [13,14]. Considering lack of data regarding the frequency of DPYD polymorphism in our colorectal patients and its association with 5FU-associated toxicity, the aim of this study was to determine three allelic variants of DPYD (IVS14+1 G>A, 2846 A>T and 2194 G>A mutation) and their association with ADRs of chemotherapy regimen containing 5FU in a group of colorectal cancer patients in North of Iran

Materials and Methods
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