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Combination-oriented molecular-targeting prevention of cancer: a model involving the combination of TRAIL and a DR5 inducer

机译:癌症的组合导向分子靶向预防:涉及TRAIL和DR5诱导剂组合的模型

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摘要

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.
机译:恶性肿瘤具有很高的死亡风险,而恶性肿瘤的预防是预防医学中的关键问题。为此,已经测试了许多化学预防药物,但是发现单一药物的作用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以协同增强单独使用化学预防剂的预防作用。为了为治疗医师提供选择最有效药物进行组合的指导,我们提出了一种策略,我们将其称为“面向组合分子靶向预防”癌症。作为模型的分子靶标,我们研究了肿瘤坏死因子相关的凋亡诱导配体(TRAIL),它特异性地导致恶性肿瘤细胞凋亡。发现这些试剂中的许多可上调死亡受体5(TRAIL受体)的表达。当与TRAIL结合使用时,还发现它们可协同诱导恶性肿瘤细胞凋亡。在此,我们坚决主张,癌症的“组合导向分子靶向预防”策略将是化学预防人类恶性肿瘤的实用方法。

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