Ho Tsing-Fen, Chang Chia-Che
Department of Medical Laboratory Science and Biotechnology, Central Taiwan University of Science and Technology, 406, Taichung, Taiwan.
Institute of Biomedical Sciences, National Chung Hsing University, No. 250, Kuo-Kuang Road, 402, Taichung, Taiwan.
Biomedicine (Taipei). 2015 Nov;5(4):23. doi: 10.7603/s40681-015-0023-8. Epub 2015 Nov 28.
An ideal cancer therapy specifically targets cancer cells while sparing normal tissues. Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) elicits apoptosis by engaging its cognate death receptors (DRs-namely, DR4 and DR5. The cancer cell-selective proapoptotic action of TRAIL is highly attractive for cancer therapy, but clinical application of TRAIL is rather limited due to tumors' inherent or acquired TRAIL resistance. Combining TRAIL with agents that reverse resistance to it has proved promising in the sensitization of TRAIL-induced apoptosis. Noteworthy, natural compounds have already been validated as potential resources for TRAIL sensitizers. In this review, we focus on the recently identified TRAILsensitizing effect of tanshinones, the anticancer ingredients of the medicinal plant Salvia miltiorrhiza (Danshen in Chinese). Research from our laboratories and others have revealed the synergy of a tanshinones-TRAIL combination in diverse types of cancer cells through up-regulation of DR5 and/or down-regulation of antiapoptotic proteins such as survivin. Thus, in addition to their anticancer mechanisms, tanshinones as TRAIL sensitizers hold great potential to be translated to TRAIL-based therapeutic modalities for combatting cancer.
理想的癌症治疗方法是特异性地靶向癌细胞,同时不损伤正常组织。肿瘤坏死因子相关凋亡诱导配体(TRAIL)通过与其同源死亡受体(即DR4和DR5)结合来引发凋亡。TRAIL对癌细胞具有选择性促凋亡作用,这对癌症治疗极具吸引力,但由于肿瘤固有的或获得性的TRAIL抗性,TRAIL的临床应用相当有限。将TRAIL与逆转其抗性的药物联合使用已被证明在增强TRAIL诱导的凋亡方面很有前景。值得注意的是,天然化合物已被证实是TRAIL增敏剂的潜在来源。在这篇综述中,我们重点关注丹参(中药)中抗癌成分丹参酮最近被发现的TRAIL增敏作用。我们实验室和其他机构的研究表明,丹参酮与TRAIL联合使用在多种类型的癌细胞中具有协同作用,可通过上调DR5和/或下调抗凋亡蛋白(如生存素)来实现。因此,除了其抗癌机制外,丹参酮作为TRAIL增敏剂在转化为基于TRAIL的抗癌治疗模式方面具有巨大潜力。