Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12188/7862
Title: Etiopathogenesis of Differentiated Thyroid Carcinomas
Authors: Makazlieva, Tanja 
Vaskova, Olivija 
Majstorov, Venjamin 
Keywords: papillary thyroid carcinoma,
follicular thyroid carcinoma,
radiation exposure,
MAPK signalling network,
PI3K-AKT pathway
Issue Date: 2-Aug-2016
Publisher: Open Access Macedonian Journal of Medical Sciences
Journal: Open Access Macedonian Journal of Medical Sciences 
Abstract: INTRODUCTION: Thyroid malignomas are a heterogeneous group of neoplasm consisting of most frequent differentiated encountered carcinomas, papillary and follicular thyroid carcinoma, then medullary thyroid carcinoma originating from neuroendocrine calcitonin-producing C-cells and rare forms of thyroid lymphomas arising from intrathyroidal lymphatic tissue, thyroid sarcomas and poorly differentiated anaplastic thyroid carcinoma. There are increasing numbers of epidemiological studies and publications that have suggested increased incidence rate of thyroid carcinomas. We have read, analysed and compare available reviews and original articles investigating different etiological factors in the development of thyroid carcinomas through Google Scholar and PubMed Database. DISCUSSION: Aetiology involved in the development of thyroid carcinomas is multifactorial and includes external influences, as well as constitutional predispositions and genetic etiological factors. The actual effect of environmental and constitutional factors is on promoting genetic and epigenetic alterations which result in cell proliferation and oncogenesis. Until now are identified numerous genetic alterations, assumed to have an important role in oncogenesis, with MAPK and PI3K-AKT as crucial signalling networks regulating growth, proliferation, differentiation and cell survival/apoptosis. CONCLUSION: This new molecular insight could have a crucial impact on diagnosis and also on improving and selecting an appropriate treatment to the patients with thyroid malignancies.
URI: http://hdl.handle.net/20.500.12188/7862
DOI: 10.3889/oamjms.2016.086
Appears in Collections:Faculty of Medicine: Journal Articles

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