The molecular pathology of thyroid neoplasms

Authors

  • JB Thapa Department of Pathology, Himal Hospital Pvt. Ltd., Kathmandu

DOI:

https://doi.org/10.3126/jpn.v4i7.10317

Keywords:

Thyroid, Tumours, Bethesda System, RAS, BRAF, p53, B Catenin, PAX8/PPAR?, Biological behavior, Gene therapy

Abstract

The Bethesda system of reporting thyroid cytology is being currently adopted worldwide. Rapid advances have been made in the understanding of the genetics of thyroid cancers. Common genetic mutations include RAS, BRAF, p53, B Catenin, and PAX8/PPARγ, genes. BRAF mutations tumours are often aggressive. BRAF mutations commonly affect papillary carcinomas in the BRAF MEK ERF intracellular pathway, whereas RAS mutations commonly affect follicular carcinoma in the PL3 kinase pathway. TK inhibitors, RAS, RET, non RET, PL3, HDAC, DNMT etc. inhibitors are also being considered for therapy against these tumours.

DOI: http://dx.doi.org/10.3126/jpn.v4i7.10317

Journal of Pathology of Nepal (2014) Vol. 4, 580-583  

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Published

2014-04-30

How to Cite

Thapa, J. (2014). The molecular pathology of thyroid neoplasms. Journal of Pathology of Nepal, 4(7), 580–583. https://doi.org/10.3126/jpn.v4i7.10317

Issue

Section

Review Articles

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