| Literature DB >> 25260367 |
Kun-Tai Hsu1, Xiao-Min Yu1, Anjon W Audhya1, Juan C Jaume1, Ricardo V Lloyd1, Shigeki Miyamoto1, Tomas A Prolla1, Herbert Chen2.
Abstract
Anaplastic thyroid cancer (ATC), accounting for less than 2% of all thyroid cancer, is responsible for the majority of death from all thyroid malignancies and has a median survival of 6 months. The resistance of ATC to conventional thyroid cancer therapies, including radioiodine and thyroid-stimulating hormone suppression, contributes to the very poor prognosis of this malignancy. This review will cover several cellular signaling pathways and mechanisms, including RET/PTC, RAS, BRAF, Notch, p53, and histone deacetylase, which are identified to play roles in the transformation and dedifferentiation process, and therapies that target these pathways. Lastly, novel approaches and agents involving the Notch1 pathway, nuclear factor κB, Trk-fused gene, cancer stem-like cells, mitochondrial mutation, and tumor immune microenvironment are discussed. With a better understanding of the biological process and treatment modality, the hope is to improve ATC outcome in the future. ©AlphaMed Press.Entities:
Keywords: Anaplastic thyroid cancer; Clinical trials; Histone deacetylase inhibitors; Kinase inhibitors; Notch; Thyroid cancer
Mesh:
Substances:
Year: 2014 PMID: 25260367 PMCID: PMC4221369 DOI: 10.1634/theoncologist.2014-0182
Source DB: PubMed Journal: Oncologist ISSN: 1083-7159