Can short-term dietary restriction and fasting have a long-term anticarcinogenic effect?

Simon Klebanov
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引用次数: 25

Abstract

Long-term dietary restriction (DR) robustly inhibits various types of carcinogenesis in rodents. Because malignancies are a major cause of death in humans, reducing the incidence or, at least, delaying the time of onset of neoplasia may significantly increase longevity of a large proportion of the human population. Long-term DR may not however be practical in humans and, judging from religious practices, several days of fasting to several weeks of DR is what a large segment of the human population can adhere to. In contrast to long-term DR, a single episode of fasting or several fasting-refeeding cycles did not have any long-lasting beneficial and usually had even a deleterious effect on carcinogenesis in rodent models. On the other hand, DR of a relatively short (1-3 months) duration often significantly increased latency and reduced the incidence of cancer over the entire life span. These results suggest that the immediate anticarcinogenic action of DR is to slow down the expansion of initiated clones, but that several months of DR may be sufficient for the elimination of a significant portion of initiated precancerous clones through apoptosis. The development of optimized DR regimens for humans will be contingent on further advances in our understanding of the mechanisms of cancer suppression by DR.

短期的饮食限制和禁食是否有长期的抗癌效果?
长期饮食限制(DR)对啮齿类动物多种类型的癌变有明显的抑制作用。由于恶性肿瘤是人类死亡的一个主要原因,减少肿瘤的发病率或至少推迟肿瘤的发病时间可能会显著延长很大一部分人口的寿命。然而,长期的DR可能并不适用于人类,从宗教习俗来看,禁食几天到几周的DR是很大一部分人可以坚持的。与长期DR相比,在啮齿动物模型中,单次禁食或几次禁食-再进食周期对致癌性没有任何长期的有益作用,通常甚至有有害作用。另一方面,相对较短(1-3个月)的DR通常会显著增加潜伏期,并降低整个生命周期的癌症发病率。这些结果表明,DR的直接抗癌作用是减缓启动克隆的扩张,但几个月的DR可能足以通过细胞凋亡消除相当一部分启动的癌前克隆。优化人类抗癌药方案的发展将取决于我们对抗癌药抑制机制的进一步了解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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