首页> 外文期刊>Molecular and Cellular Endocrinology >Radiosensitivity enhancement of human thyroid carcinoma cells by the inhibitors of histone deacetylase sodium butyrate and valproic acid
【24h】

Radiosensitivity enhancement of human thyroid carcinoma cells by the inhibitors of histone deacetylase sodium butyrate and valproic acid

机译:由组蛋白脱乙酰化酶丁酸钠和丙戊酸钠的抑制剂对人甲状腺癌细胞的放射敏感性提高

获取原文
获取原文并翻译 | 示例
           

摘要

Radiotherapy is one of the leading treatments for clinical cancer therapy. External beam radiotherapy has been proposed as an adjuvant treatment for patients bearing differentiated thyroid cancer refractory to conventional therapy. Our purpose was to study the combined effect of HDAC inhibitors (HDACi) and ionizing irradiation in thyroid cancer cell lines (Nthy-ori 3-1, WRO, TPC-1 and 8505c). HDACi radiosensitized thyroid cancer cells as evidenced by the reduction of survival fraction, whereas they had no effect in the normal cells. HDACi enhanced radiation-induced cell death in WRO cells. Gamma-H2AX foci number increased and persisted long after ionizing exposure in the HDACi-treated cells (WRO and TPC-1). Moreover, the expression of the repair-related gene Ku80 was differentially modulated only in the cancer cells, by the compounds at the protein and/or mRNA levels. We present in vitro evidence that HDACi can enhance the radiosensitivity of human thyroid cancer cells.
机译:放射疗法是临床癌症治疗的主要处理之一。 外部光束放射治疗已提出为患有含有分化的甲状腺癌难以传统治疗的辅助治疗。 我们的目的是研究HDAC抑制剂(HDACI)和电离辐照的综合作用(nthy-ori 3-1,Wro,TPC-1和8505c)。 HDACI辐射敏化甲状腺癌细胞,其通过减少存活率馏分证明,而它们在正常细胞中没有作用。 HDACI增强了WRO细胞中的辐射诱导的细胞死亡。 在HDACI处理的细胞(WRO和TPC-1)中电离暴露后,γ-H2AX焦点数量增加并持续存在。 此外,通过蛋白质和/或mRNA水平的化合物在癌细胞中仅在癌细胞中差异调节修复相关基因Ku80的表达。 我们存在体外证据证明HDACI可以增强人甲状腺癌细胞的放射敏感性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号