| Literature DB >> 29408820 |
Ewa Chmielik1, Dagmara Rusinek2, Malgorzata Oczko-Wojciechowska2, Michal Jarzab3, Jolanta Krajewska2, Agnieszka Czarniecka4, Barbara Jarzab2.
Abstract
There are 5 main histological types of thyroid cancers (TCs): papillary, follicular (also known as differentiated), poorly differentiated, anaplastic (the most aggressive form), and medullary TC, and only the latter arises from thyroid C cells. These different forms of TCs show significant variability, both among and within tumours. This great variation is particularly notable among the first 4 types, which all originate from thyroid follicular cells. Importantly, this heterogeneity is not limited to histopathological diversity only but is also manifested as variation in several genetic and/or epigenetic alterations, the numbers of interactions between the tumour and surrounding microenvironment, and interpatient differences, for example. All these factors contribute to the great complexity in the development of a tumour from cancer cells. In the present review, we summarise the knowledge accumulated about the heterogeneity of TCs. Further research in this direction should help to gain a better understanding of the underlying mechanisms contributing to the development and diversity of TCs, paving the way toward more effective treatment strategies.Entities:
Keywords: BRAF mutation; Heterogeneity; RAS mutation; Thyroid cancer
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Year: 2018 PMID: 29408820 DOI: 10.1159/000486422
Source DB: PubMed Journal: Pathobiology ISSN: 1015-2008 Impact factor: 4.342