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内静氨酸:一种血管生成和瘤生长的内源性抑制剂
M S O'Reilly1, T Boehm, Y Shing
1Department of Surgery, Children's Hospital, Boston, Massachusetts 02115, USA.
Cell
|January 24, 1997
概括
研究人员发现了内静氨酸,一种来自原XVIII的血管生成抑制剂,它有效地阻止了瘤生长和血管生成. 这一发现验证了用于识别内源性血管生成抑制剂的新策略,并证明了休眠疗法的潜力.
科学领域:
- 在瘤学瘤学.
- 分子生物学分子生物学
- 生物化学 生物化学
背景情况:
- 血管新生对于瘤生长和转移至关重要.
- 内源性血管生成抑制剂是一个有前途的治疗策略.
- 之前对血管静止素的鉴定为发现类似的抑制剂铺平了道路.
研究的目的:
- 为了确定新的内源性血管生成抑制剂.
- 描述内静素的抗血管和抗瘤特性.
- 用一种新的输送方法评估内静止素的治疗潜力.
主要方法:
- 使用类似于血管静止素识别的策略.
- 隔离和鉴定了 XVIII 原的一小部分内静止素.
- 由大肠杆菌衍生的内静止素通过持续释放作为非重新折叠的悬浮剂进行了施用.
- 瘤回归,血管生成,增殖和亡通过免疫组织化学评估.
主要成果:
- 内静止素特异性抑制了内皮细胞的增殖和血管生成.
- 给予内静止素导致原发性瘤回归到休眠病变.
- 免疫组织化学证实了阻断血管生成和瘤细胞中的增殖和亡的平衡.
- 没有观察到显著的毒性.
结论:
- 内静氨酸是一种强大的内源性血管生成和瘤生长抑制剂.
- 这些发现验证了识别内源性血管生成抑制剂的策略.
- 蛋白质碎片代表了一类潜在的血管生成抑制剂.
- 持续释放的内静止素证明了瘤的有效休眠疗法.
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