1 / 24

抑制 HO-1 增强 As2O3 对胶质瘤疗效的实验研究

抑制 HO-1 增强 As2O3 对胶质瘤疗效的实验研究. 刘耀华 陈晓丰 梁元 郑秉杰 赵世光. 哈尔滨医科大学附属第一医院 神经外科. It was proved that subarachnoid injection of As 2 O 3 is safe. Intraoperative transplantation of Ommaya device (ACNU or ACNU+As 2 O 3 ). Preoperation. 47 male, Grade Ⅲ-Ⅳ :

harvey
Download Presentation

抑制 HO-1 增强 As2O3 对胶质瘤疗效的实验研究

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. 抑制HO-1增强As2O3对胶质瘤疗效的实验研究 刘耀华 陈晓丰 梁元 郑秉杰 赵世光 哈尔滨医科大学附属第一医院 神经外科

  2. It was proved that subarachnoid injection of As2O3 is safe.

  3. Intraoperative transplantation of Ommaya device (ACNU or ACNU+As2O3)

  4. Preoperation 47 male, Grade Ⅲ-Ⅳ: Ommaya device (ACNU+As2O3), Arterial chemotherapy (As2O3), and Radiotherapy One year after operation

  5. Recurrent glioma 54 female, Grade Ⅲ: Ommaya device (ACNU+As2O3), Arterial chemotherapy (As2O3), and Radiotherapy 6 months after the second operation

  6. Preoperation 47 female, Grade Ⅲ-Ⅳ: Ommaya device (ACNU+As2O3), Arterial chemotherapy (As2O3), and Radiotherapy 2 years after operation

  7. 44 male, Grade Ⅲ: Ommaya device (ACNU+As2O3), Arterial chemotherapy (As2O3), and Radiotherapy Case3 MRI before operation Before operative MRI CT one week after operative and the first chemotherapy Preoperative CT CT one and half a year after operation

  8. 研究背景 三氧化二砷(As2O3)与肿瘤治疗 • 国内外研究发现As2O3在实体肿瘤治疗受到限制,小剂量药物不能达到治疗效果,而增大剂量往往增加药物毒性; • As2O3作用于细胞后不仅引起细胞毒性效应,同时还激活细胞内一些保护性分子和信号通路; • As2O3诱导细胞凋亡的机制被认为主要是通过活性氧(ROS)的诱导而实现; • ROS可以诱导细胞保护性分子血红素加氧酶-1(HO-1); • HO-1在胶质瘤中广泛表达; • 抑制HO-1是否可以提高As2O3对胶质瘤的治疗效果?

  9. 实验设计 • 胶质瘤细胞系U251MG用As2O3处理,检测细胞活性、线粒体膜电位(MMP),并观察ROS清除剂LNAC对细胞是否有保护作用; • 检测As2O3诱导胶质瘤细胞ROS生成、MAPK信号通路的活化,HO-1的诱导以及LNAC对其影响; • 使用HO-1的诱导剂和抑制剂处理细胞,观察其对As2O3效应的影响; • Nrf2是HO-1表达的重要转录因子,SiRNA技术干扰Nrf2表达后对比细胞对As2O3的敏感性。

  10. Cell Viability ** P<0.01 compared with control; ▼P<0.01 compared with LNAC untreated cells.

  11. Mitochondrial Membrane Potential

  12. Sub-G1 (PI Staining)

  13. ROS induction

  14. Downstreams of ROS

  15. Nrf2 Translocation

  16. Effects of HO-1 inducer * P<0.01

  17. Effects of HO-1 inducer * P<0.01

  18. Effects of HO-1 inhibitor * P<0.01 * P<0.01

  19. Knockdown of Nrf2 ATO (5uM) Random Nrf2 Random Nrf2 0h 3h 6h 0h 3h 6h HO-1 Nrf2 b-actin GAPDH

  20. Knockdown of Nrf2 * P<0.01

  21. Knockdown of Nrf2

  22. Knockdown of Nrf2 * P<0.01

  23. Cell death ROS Nrf2 activation ATO HO-1 induction

More Related