Department of Molecular-Targeting Cancer Prevention, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kawaramachi-Hirokoji, Kamigyo-ku, Kyoto, 602-8566, Japan.
Environ Health Prev Med. 2010 Jul;15(4):203-10. doi: 10.1007/s12199-009-0128-3. Epub 2010 Jan 6.
Malignant tumors carry a high risk of death, and the prevention of malignant tumors is a crucial issue in preventive medicine. To this end, many chemopreventive agents have been tested, but the effects of single agents have been found to be insufficient to justify clinical trials. We have therefore hypothesized that combinations of different chemopreventive agents may synergistically enhance the preventive effect of chemopreventive agents used singly. To provide the treating physician with some guideline by which to choose the most effective agents to be combined, we propose a strategy which we have termed the "combination-oriented molecular-targeting prevention" of cancer. As the molecular target of our model, we focused on tumor necrosis factor-related apoptosis-inducing ligand (TRAIL), which specifically causes apoptosis in malignant tumor cells. Many of these agents were found to up-regulate the expression of death receptor 5, a TRAIL receptor. They were also found to synergistically induce apoptosis in malignant tumor cells when combined with TRAIL. Here, we strongly advocate that the strategy of "combination-oriented molecular-targeting prevention" of cancer will be a practical approach for chemoprevention against human malignant tumors.
恶性肿瘤具有很高的死亡风险,预防恶性肿瘤是预防医学中的一个关键问题。为此,已经测试了许多化学预防剂,但发现单一药物的效果不足以证明临床试验的合理性。因此,我们假设不同化学预防剂的组合可能会协同增强单独使用的化学预防剂的预防效果。为了为治疗医生提供一些指导,以便选择最有效的联合药物,我们提出了一种我们称之为“癌症联合导向分子靶向预防”的策略。作为我们模型的分子靶点,我们专注于肿瘤坏死因子相关凋亡诱导配体(TRAIL),它特异性地导致恶性肿瘤细胞凋亡。许多这些药物被发现上调 TRAIL 受体死亡受体 5 的表达。当与 TRAIL 联合使用时,它们还被发现协同诱导恶性肿瘤细胞凋亡。在这里,我们强烈主张“癌症联合导向分子靶向预防”策略将是预防人类恶性肿瘤的实用方法。