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Synergy between HDAC and PARP Inhibitors on Proliferation of a Human Anaplastic Thyroid Cancer-Derived Cell Line

机译:HDAC和PARP抑制剂对人间变性甲状腺癌衍生细胞系增殖的协同作用

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摘要

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.
机译:间变性甲状腺癌(ATC)是一种非常具有侵略性的人类恶性肿瘤,具有明显的浸润性,并且没有甲状腺分化的特征。已知HDAC抑制剂或PARP抑制剂对甲状腺癌细胞具有抗增殖作用。因此,在这项研究中,已经研究了两种化合物之间可能的协同作用。 ATC衍生的细胞系SW1736已单独或组合用HDAC抑制剂辛二酰苯胺异羟肟酸(SAHA)和PARP抑制剂PJ34处理。就细胞生存力而言,各种测试剂量下的组合指数值始终低于1,因此表明这两种化合物在多种剂量下均具有协同作用。在诱导凋亡中也观察到协同作用。就甲状腺特异性基因表达而言,在TSHR mRNA水平上观察到协同作用,但在NIS,TTF1,TTF2和PAX8 mRNA水平上观察不到协同作用。总之,这些数据表明,HDAC和PARP抑制剂的联合使用可能是治疗ATC的有用策略。

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