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Designing a broad-spectrum integrative approach for cancer prevention and treatment

机译:设计用于癌症预防和治疗的广谱整合方法

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摘要

Targeted therapies and the consequent adoption of "personalized" oncology have achieved notable successes in some cancers; however, significant problems remain with this approach. Many targeted therapies are highly toxic, costs are extremely high, and most patients experience relapse after a few disease-free months. Relapses arise from genetic heterogeneity in tumors, which harbor therapy-resistant immortalized cells that have adopted alternate and compensatory pathways (i.e., pathways that are not reliant upon the same mechanisms as those which have been targeted). To address these limitations, an international task force of 180 scientists was assembled to explore the concept of a low-toxicity "broadspectrum" therapeutic approach that could simultaneously target many key pathways and mechanisms. Using cancer hallmark phenotypes and the tumor microenvironment to account for the various aspects of relevant cancer biology, interdisciplinary teams reviewed each hallmark area and nominated a wide range of high-priority targets (74 in total) that could be modified to improve patient outcomes. For these targets, corresponding low-toxicity therapeutic approaches were then suggested, many of which were phytochemicals. Proposed actions on each target and all of the approaches were further reviewed for known effects on other hallmark areas and the tumor microenvironment Potential contrary or procarcinogenic effects were found for 3.9% of the relationships between targets and hallmarks, and mixed evidence of complementary and contrary relationships was found for 7.1%. Approximately 67% of the relationships revealed potentially complementary effects, and the remainder had no known relationship. Among the approaches, 1.1% had contrary, 2.8% had mixed and 62.1% had complementary relationships. These results suggest that a broad-spectrum approach should be feasible from a safety standpoint. This novel approach has potential to be relatively inexpensive, it should help us address stages and types of cancer that lack conventional treatment, and it may reduce relapse risks. A proposed agenda for future research is offered. (C) 2015 The Authors. Published by Elsevier Ltd.
机译:针对性疗法和随后采用“个性化”肿瘤学已在某些癌症中取得了显著成功;但是,这种方法仍然存在很多问题。许多靶向疗法具有剧毒,成本非常高,并且大多数患者在数月无病后会复发。复发是由肿瘤的遗传异质性引起的,肿瘤具有不育的永生化细胞,这些细胞采用了交替的和补偿性的途径(即不依赖于已靶向的机制的途径)。为了解决这些局限性,由180名科学家组成的国际工作组组建了一个低毒“广谱”治疗方法的概念,该方法可同时针对许多关键途径和机制。跨学科研究小组使用癌症标志物表型和肿瘤微环境来说明相关癌症生物学的各个方面,跨学科小组审查了每个标志物区域,并提名了可以修改以改善患者预后的广泛的高优先级靶标(共74个)。对于这些靶标,随后提出了相应的低毒性治疗方法,其中许多是植物化学物质。进一步审查了对每个靶标和所有方法的拟议行动,以了解对其他标志区域的已知作用,并且在肿瘤微环境中发现了3.9%的靶标与标志之间的关系具有潜在的相反或致癌作用,并且存在互补和相反关系的混合证据被发现为7.1%。大约67%的关系显示出潜在的互补效应,其余的关系未知。在这些方法中,有1.1%表示相反,2.8%表示混合,62.1%表示互补。这些结果表明,从安全角度出发,广谱方法应该是可行的。这种新颖的方法具有相对便宜的潜力,它应该可以帮助我们解决缺乏常规治疗方法的癌症分期和类型,并且可以降低复发风险。提供了拟议的未来研究议程。 (C)2015作者。由Elsevier Ltd.发布

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