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雷公藤甲素通过抑制核因子κB激活使肺癌细胞对肿瘤坏死因子相关凋亡诱导配体(TRAIL)诱导的凋亡敏感化。

Triptolide sensitizes lung cancer cells to TNF-related apoptosis-inducing ligand (TRAIL)-induced apoptosis by inhibition of NF-kappaB activation.

作者信息

Lee Kye Young, Park Jae Seuk, Jee Young Koo, Rosen Glenn D

机构信息

Department of Internal Medicine, Dankook University College of Medicine, Cheonan, Korea.

出版信息

Exp Mol Med. 2002 Dec 31;34(6):462-8. doi: 10.1038/emm.2002.64.

Abstract

TNF-related apoptosis-inducing ligand (TRAIL/Apo- 2L), a newly identified member of the TNF family promotes apoptosis by binding to the transmembrane receptors (TRAIL-R1/DR4 and TRAIL-R2/DR5). TRAIL known to activate NF-kappaB in number of tumor cells including A549 (wt p53) and NCI-H1299 (null p53) lung cancer cells exerts relatively selective cytotoxic affects to the human tumor cell lines without much effect on the normal cells. We set out to identify an agent that would sensitize lung cancer cells to TRAIL-induced apoptosis through inhibition of NF-kappaB activation. We found that triptolide, an oxygenated diterpene extracted and purified from the Chinese herb Tripterygium wilfordii sensitized A549 and NCI-H1299 cells to TRAIL-induced apoptosis through inhibition of NF-kappaB activation. Pretreatment with MG132 which is a well-known NF-kappaB inhibitor by blocking degradation of IkappaBalpha also greatly sensitized lung cancer cells to TRAIL-induced apoptosis. Triptolide did not block DNA binding of NF-kappaB activated by TRAIL as in the case of TNF-alpha. It has been already proven that triptolide blocks transactivation of p65 which plays a key role in NF-kappaB activation. These observations suggest that triptolide may be a potentially useful drug to enhance TRAIL-induced tumor killing in lung cancer.

摘要

肿瘤坏死因子相关凋亡诱导配体(TRAIL/Apo - 2L)是肿瘤坏死因子家族新发现的成员,通过与跨膜受体(TRAIL - R1/DR4和TRAIL - R2/DR5)结合来促进细胞凋亡。已知TRAIL可在包括A549(野生型p53)和NCI - H1299(p53缺失)肺癌细胞在内的多种肿瘤细胞中激活核因子κB,它对人类肿瘤细胞系具有相对选择性的细胞毒性作用,而对正常细胞影响不大。我们着手寻找一种能够通过抑制核因子κB激活使肺癌细胞对TRAIL诱导的凋亡敏感的药物。我们发现,从中药雷公藤中提取纯化的氧化二萜类化合物雷公藤内酯醇,可通过抑制核因子κB激活使A549和NCI - H1299细胞对TRAIL诱导的凋亡敏感。用MG132(一种通过阻断IκBα降解来抑制核因子κB的知名抑制剂)预处理也能极大地使肺癌细胞对TRAIL诱导的凋亡敏感。与肿瘤坏死因子α的情况不同,雷公藤内酯醇不会阻断TRAIL激活的核因子κB与DNA的结合。已经证实雷公藤内酯醇可阻断在核因子κB激活中起关键作用的p65的反式激活。这些观察结果表明,雷公藤内酯醇可能是一种潜在有用的药物,可增强TRAIL诱导的肺癌肿瘤杀伤作用。

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