4.6 Article

Association of MTHFR and TYMS gene polymorphisms with the susceptibility to HCC in Egyptian HCV cirrhotic patients

Journal

CLINICAL AND EXPERIMENTAL MEDICINE
Volume 22, Issue 2, Pages 257-267

Publisher

SPRINGER-VERLAG ITALIA SRL
DOI: 10.1007/s10238-021-00747-3

Keywords

Hepatitis C virus (HCV); Hepatocellular carcinoma (HCC); Methylenetetrahydrofolate reductase (MTHFR); Thymidylate synthase (TYMS); Polymorphism

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The study found that MTHFR c.677C>T and c.1298A>C gene polymorphisms may influence the susceptibility to HCV-related HCC in the Egyptian population, aiding in the early diagnosis and management of the disease.
Identification of host genetic factors influencing the risk of developing hepatocellular carcinoma (HCC) in patients with chronic hepatitis C virus (HCV) infection may help to refine patients' selection to benefit from specific preventative measures and/or adapted screening policies. Thus, this study aimed to investigate the association of MTHFR c.677C>T and c.1298A>C in addition to TYMS 3 '-UTR 6-bp ins/del polymorphisms with the susceptibility to HCV-related HCC in an Egyptian population. Polymerase chain reaction-restriction fragment length polymorphism was performed to genotype the polymorphisms in 194 HCV-infected patients subdivided into liver cirrhotic (LC, n=104) and HCC (n=90) patients as well as 100 healthy subjects. In healthy controls, the MTHFR c.677C>T polymorphism under the homozygous and recessive models (p=0.005) and the c.1298A>C polymorphism under all the tested genetic models (p-values range from<0.001 to 0.007) were associated with an increased risk of HCC. In LC patients, the MTHFR c.677C>T polymorphism under the homozygous, dominant, and recessive models (p-values range from 0.001 to 0.007), as well as MTHFR c.1298A>C under the homozygous model only (p=0.014), increased the susceptibility to HCC. The C/C and T/C haplotypes of MTHFR c.677C>T and MTHFR c.1298A>C polymorphisms were contributed to an increased risk of healthy subjects to develop HCC (p-values range from<0.001 to 0.015), while only the T/C haplotype was associated with the progression of HCC in LC patients (p=0.001). In conclusion, MTHFR c.677C>T and c.1298A>C in addition to their haplotypes may contribute to the development of HCV-related HCC in an Egyptian population. These findings may aid in the early diagnosis and management of HCC.

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