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Genetic susceptibility to hereditary non-medullary thyroid cancer.

Tina KamaniParsa CharkhchiAfshan ZahediMohammadreza Akbari
Published in: Hereditary cancer in clinical practice (2022)
Non-medullary thyroid cancer (NMTC) is the most common type of thyroid cancer. With the increasing incidence of NMTC in recent years, the familial form of the disease has also become more common than previously reported, accounting for 5-15% of NMTC cases. Familial NMTC is further classified as non-syndromic and the less common syndromic FNMTC. Although syndromic NMTC has well-known genetic risk factors, the gene(s) responsible for the vast majority of non-syndromic FNMTC cases are yet to be identified. To date, several candidate genes have been identified as susceptibility genes in hereditary NMTC. This review summarizes genetic predisposition to non-medullary thyroid cancer and expands on the role of genetic variants in thyroid cancer tumorigenesis and the level of penetrance of NMTC-susceptibility genes.
Keyphrases
  • genome wide
  • intellectual disability
  • risk factors
  • copy number
  • dna methylation
  • genome wide identification
  • autism spectrum disorder
  • early onset
  • transcription factor