Chinese Journal of Lung Cancer (Dec 2017)

Detection of UGT1A1*28 Polymorphism Using Fragment Analysis

  • Ying HUANG,
  • Jian SU,
  • Xiaosui HUANG,
  • Danxia LU,
  • Zhi XIE,
  • Suqing YANG,
  • Weibang GUO,
  • Zhiyi LV,
  • Hongsui WU,
  • Xuchao ZHANG

DOI
https://doi.org/10.3779/j.issn.1009-3419.2017.12.04
Journal volume & issue
Vol. 20, no. 12
pp. 817 – 821

Abstract

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Background and objective Uridine-diphosphoglucuronosyl transferase 1A1 (UGT1A1), UGT1A1*28 polymorphism can reduce UGT1A1 enzymatic activity, which may lead to severe toxicities in patients who receive irinotecan. This study tries to build a fragment analysis method to detect UGT1A1*28 polymorphism. Methods A total of 286 blood specimens from the lung cancer patients who were hospitalized in Guangdong General Hospital between April 2014 to May 2015 were detected UGT1A1*28 polymorphism by fragment analysis method. Results Comparing with Sanger sequencing, precision and accuracy of the fragment analysis method were 100%. Of the 286 patients, 236 (82.5% harbored TA6/6 genotype, 48 (16.8%) TA 6/7 genotype and 2 (0.7%) TA7/7 genotype. Conclusion Our data suggest hat the fragment analysis method is robust for detecting UGT1A1*28 polymorphism in clinical practice. It’s simple, time-saving, and easy-to-carry.

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