Department of Pathology, Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI 48201, USA.
Cancers (Basel). 2011 Jul 19;3(3):2955-74. doi: 10.3390/cancers3032955.
Indole compounds, obtained from cruciferous vegetables, are well-known for their anti-cancer properties. In particular, indole-3-carbinol (I3C) and its dimeric product, 3,3´-diindolylmethane (DIM), have been widely investigated for their effectiveness against a number of human cancers in vitro as well as in vivo. These compounds are effective inducers of apoptosis and the accumulating evidence documenting their ability to modulate multiple cellular signaling pathways is a testimony to their pleiotropic behavior. Here we attempt to update current understanding on the various mechanisms that are responsible for the apoptosis-inducing effects by these compounds. The significance of apoptosis-induction as a desirable attribute of anti-cancer agents such as indole compounds cannot be overstated. However, an equally intriguing property of these compounds is their ability to sensitize cancer cells to standard chemotherapeutic agents. Such chemosensitizing effects of indole compounds can potentially have major clinical implications because these non-toxic compounds can reduce the toxicity and drug-resistance associated with available chemotherapies. Combinational therapy is increasingly being realized to be better than single agent therapy and, through this review article, we aim to provide a rationale behind combination of natural compounds such as indoles with conventional therapeutics.
吲哚类化合物,从十字花科蔬菜中获得,以其抗癌特性而闻名。特别是吲哚-3-甲醇(I3C)及其二聚体产物 3,3'-二吲哚基甲烷(DIM),因其对体外和体内多种人类癌症的有效性而被广泛研究。这些化合物是有效的细胞凋亡诱导剂,越来越多的证据表明它们能够调节多种细胞信号通路,证明了它们的多效性。在这里,我们试图更新目前对这些化合物诱导细胞凋亡的各种机制的理解。细胞凋亡诱导作为抗癌药物(如吲哚类化合物)的理想特性,其重要性怎么强调都不为过。然而,这些化合物的另一个同样有趣的特性是它们能够使癌细胞对标准化疗药物敏感。吲哚类化合物的这种化疗增敏作用可能具有重要的临床意义,因为这些非毒性化合物可以降低现有化疗药物相关的毒性和耐药性。联合治疗越来越被认为优于单一药物治疗,通过这篇综述文章,我们旨在为将天然化合物(如吲哚类化合物)与常规疗法联合使用提供一个理论依据。