Frontiers in Genetics (Aug 2020)

A Pilot Study on the Whole Exome Sequencing of Prostate Cancer in the Indian Phenotype Reveals Distinct Polymorphisms

  • Ayam Gupta,
  • Ayam Gupta,
  • Nidhi Shukla,
  • Nidhi Shukla,
  • Mamta Nehra,
  • Sonal Gupta,
  • Babita Malik,
  • Ashwani Kumar Mishra,
  • Maneesh Vijay,
  • Jyotsna Batra,
  • Nirmal Kumar Lohiya,
  • Devendra Sharma,
  • Prashanth Suravajhala

DOI
https://doi.org/10.3389/fgene.2020.00874
Journal volume & issue
Vol. 11

Abstract

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Prostate cancer (PCa) is the third most common cancer among men in India, and no next-generation sequencing (NGS) studies have been attempted earlier. Recent advances in NGS have heralded the discovery of biomarkers from Caucasian/European and Chinese ancestry, but not much is known about the Indian phenotype/variant of PCa. In a pilot study using the whole exome sequencing of benign/PCa patients, we identified characteristic mutations specific to the Indian sub-population. We observed a large number of mutations in DNA repair genes, viz. helicases, TP53, and BRCA besides the variants of unknown significance with a possibly damaging rare variant (rs730881069/chr19:55154172C/TR136Q) in the TNNI3 gene that has been previously reported as a semi-conservative amino acid substitution. Our pilot study attempts to bring an understanding of PCa prognosis and recurrence for the Indian phenotype.

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