癌症
癌细胞
癌症治疗
肿瘤坏死因子α
细胞凋亡
癌症研究
兴奋剂
内生
受体
医学
生物
免疫学
内科学
遗传学
作者
Daniel D De Carvalho,Bárbara Piffero Mello,Welbert Oliveira Pereira,Gustavo P. Amarante-Mendes
出处
期刊:Current Molecular Medicine
[Bentham Science]
日期:2013-02-01
卷期号:13 (2): 296-304
被引量:20
标识
DOI:10.2174/156652413804810727
摘要
The tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) exerts a cancer cell-specific pro-apoptotic activity. This property made the TRAIL associated pathway one of the most promising strategies aimed at inducing tumor-selective death. In fact, several approaches have been considered to explore this pathway for cancer therapy, such as recombinant TRAIL, agonist antibodies for TRAIL receptors, and adenoviral TRAIL. However, all of these approaches have certain disadvantages that limit their clinical use. Our recent discovery that the complex PRAME/EZH2 is able to repress TRAIL expression, in a cancer-specific manner, suggests an alternative approach for combined cancer therapy. A genetic or pharmacological inhibition of TRAIL repressors in cancer cells could restore endogenous TRAIL expression, thereby overcoming some of the limitations of and/or cooperating with previous approaches.
科研通智能强力驱动
Strongly Powered by AbleSci AI