Login / Signup

Investigation of DPYD , MTHFR and TYMS polymorphisms on 5-fluorouracil related toxicities in colorectal cancer.

Mehtap CevikEsat NamalNur Dinc SenerUlkuhan Iner KoksalPenbe CagatayGokce DeliormanCavlan CiftciAtila KaraalpBelgin Susleyici
Published in: Personalized medicine (2022)
Aim: To investigate the association of DPYD , MTHFR and TYMS polymorphisms on 5-fluorouracil (5-FU) related toxicities and patient survival. Materials & methods: A total of 103 colorectal cancer patients prescribed 5-FU were included in the study. Genotyping was conducted for several DPYD , MTHFR and TYMS polymorphisms using a microarray analyzer. Results: DPYD 496A>G polymorphism was found to be significantly associated with 5-FU related grade 0-2, but not severe toxicities (p = 0.02). Furthermore, patients with DPYD 85TC and CC genotypes had longer progression and overall survival times compared to TT genotypes in our study group (log rank = 6.60; p = 0.01 and log rank = 4.40; p = 0.04, respectively). Conclusion: According to our results, DPYD 496AG and GG genotypes might be protective against severe adverse events compared to the AA genotype. Another DPYD polymorphism, 85T>C, may be useful in colorectal cancer prognosis. Further studies for both polymorphisms should be conducted in larger populations to achieve accurate results.
Keyphrases
  • early onset
  • drug induced
  • high resolution
  • dna methylation
  • mass spectrometry
  • genome wide
  • free survival