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Synergy between HDAC and PARP Inhibitors on Proliferation of a Human Anaplastic Thyroid Cancer-Derived Cell Line
- Source :
- International Journal of Endocrinology, International Journal of Endocrinology, Vol 2015 (2015)
- Publication Year :
- 2015
- Publisher :
- Hindawi Publishing Corporation, 2015.
-
Abstract
- Anaplastic thyroid carcinoma (ATC) is a very aggressive human malignancy, having a marked degree of invasiveness and no features of thyroid differentiation. It is known that either HDAC inhibitors or PARP inhibitors have antiproliferative effects on thyroid cancer cells. Therefore, in this study the possible synergy between the two types of compounds has been investigated. The ATC-derived cell line SW1736 has been treated with the HDAC inhibitor suberoylanilide hydroxamic acid (SAHA) and the PARP inhibitor PJ34, alone or in combination. In terms of cell viability, the combination index value was always lower than 1 at various tested dosages, indicating, therefore, synergy in a wide range of doses for both compounds. Synergy was also observed in induction of apoptosis. In terms of thyroid-specific gene expression, synergy was observed for TSHR mRNA levels but not for NIS, TTF1, TTF2, and PAX8 mRNA levels. Altogether, these data suggest that the combined use of HDAC and PARP inhibitors may be a useful strategy for treatment of ATC.
- Subjects :
- Endocrine and Autonomic Systems
Endocrinology
thyroid carcinoma
anaplastic thyroid carcinoma
Article Subject
Endocrinology, Diabetes and Metabolism
Bioinformatics
lcsh:Diseases of the endocrine glands. Clinical endocrinology
medicine
Viability assay
Anaplastic thyroid cancer
Thyroid cancer
lcsh:RC648-665
business.industry
Thyroid
medicine.disease
Diabetes and Metabolism
medicine.anatomical_structure
Cell culture
Apoptosis
PARP inhibitor
Cancer research
PAX8
business
Research Article
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Journal :
- International Journal of Endocrinology, International Journal of Endocrinology, Vol 2015 (2015)
- Accession number :
- edsair.doi.dedup.....4fd9606343b9c28eb92e20476bde8c11