国际肿瘤学杂志 ›› 2013, Vol. 40 ›› Issue (2): 83-85.

• 综述 •    下一篇

FLIP在肿瘤中的研究

沈珏, 李玉峰, 何振娟   

  1. 200092 上海交通大学医学院附属新华医院儿内科
  • 出版日期:2013-02-08 发布日期:2013-01-25
  • 通讯作者: 李玉峰,E-mail: mieuniversity@hotmail.com E-mail:mieuniversity@hotmail.com
  • 基金资助:

    国家自然科学基金(30901737)

Research progress of FLIP in cancer

SHEN  Jue, LI  Yu-Feng, HE  Zhen-Juan   

  1. Department of Pediatrics, Xin Hua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200092, China
  • Online:2013-02-08 Published:2013-01-25
  • Contact: Corresponding author: LI Yu-feng, E-mail: mieuniversity@hotmail.com E-mail:mieuniversity@hotmail.com

摘要: FLIP是一种含有死亡结构域的蛋白质,人类有3个亚型c-FLIPL、c-FLIPS和c-FLIPR,是多种肿瘤细胞抑制凋亡的主要蛋白,其中c-FLIPL在细胞凋亡信号中起双重作用。FLIP的表达高低不仅可以决定细胞凋亡通路的开闭,同时也能实现细胞在凋亡信号与增殖信号通路间的转换。FLIP表达的调控是多层次的,涉及多条信号通路,有可能成为极具吸引力的死亡受体信号的治疗靶点。

关键词: FLIP, 细胞凋亡, 信号通路, 调控

Abstract: FLIP is a protein containing death domain. Human beings have three subtypes of c-FLIPL, c-FLIPS and c-FLIPR, which can inhibit the apoptosis of a variety of tumor cells. C-FLIPL plays a dual role in the apoptotic signal. The expression level of FLIP not only decides the opening and closing of the apoptosis pathway but also achieve the conversion of cells in the apoptotic signaling and proliferative signaling pathway. The regulation of FLIP’s expression is a multi-layered, involving multiple signaling pathways. FLIP will probably become an attractive death receptor signaling target of therapy.

Key words: FLIP, Apoptosis, Signaling pathway, Regulation