Semmelweis University, Department of Bioinformatics, Tűzoltó u. 7-9, H-1094 Budapest, Hungary; Research Centre for Natural Sciences, Cancer Biomarker Research Group, Institute of Enzymology, Magyar tudósok krt. 2, H-1117 Budapest, Hungary; National Laboratory for Drug Research and Development, Magyar tudósok krt. 2, H-1117 Budapest, Hungary.
Semmelweis University, Department of Bioinformatics, Tűzoltó u. 7-9, H-1094 Budapest, Hungary; Research Centre for Natural Sciences, Cancer Biomarker Research Group, Institute of Enzymology, Magyar tudósok krt. 2, H-1117 Budapest, Hungary; National Laboratory for Drug Research and Development, Magyar tudósok krt. 2, H-1117 Budapest, Hungary.
Biochim Biophys Acta Rev Cancer. 2024 Mar;1879(2):189062. doi: 10.1016/j.bbcan.2023.189062. Epub 2023 Dec 28.
Renewed interest in tumor metabolism sparked an enthusiasm for dietary interventions to prevent and treat cancer. Changes in diet impact circulating nutrient levels in the plasma and the tumor microenvironment, and preclinical studies suggest that dietary approaches, including caloric and nutrient restrictions, can modulate tumor initiation, progression, and metastasis. Cancers are heterogeneous in their metabolic dependencies and preferred energy sources and can be addicted to glucose, fructose, amino acids, or lipids for survival and growth. This dependence is influenced by tumor type, anatomical location, tissue of origin, aberrant signaling, and the microenvironment. This review summarizes nutrient dependencies and the related signaling pathway activations that provide targets for nutritional interventions. We examine popular dietary approaches used as adjuvants to anticancer therapies, encompassing caloric restrictions, including time-restricted feeding, intermittent fasting, fasting-mimicking diets (FMDs), and nutrient restrictions, notably the ketogenic diet. Despite promising results, much of the knowledge on dietary restrictions comes from in vitro and animal studies, which may not accurately reflect real-life situations. Further research is needed to determine the optimal duration, timing, safety, and efficacy of dietary restrictions for different cancers and treatments. In addition, well-designed human trials are necessary to establish the link between specific metabolic vulnerabilities and targeted dietary interventions. However, low patient compliance in clinical trials remains a significant challenge.
肿瘤代谢的新研究兴趣激发了人们对饮食干预以预防和治疗癌症的热情。饮食的改变会影响血浆和肿瘤微环境中的循环营养水平,临床前研究表明,包括热量和营养限制在内的饮食方法可以调节肿瘤的发生、进展和转移。癌症在其代谢依赖性和首选能量来源上具有异质性,并且可以依赖葡萄糖、果糖、氨基酸或脂质来生存和生长。这种依赖性受肿瘤类型、解剖位置、起源组织、异常信号和微环境的影响。这篇综述总结了营养依赖性和相关信号通路的激活,这些为营养干预提供了靶点。我们研究了作为抗癌疗法辅助手段的流行饮食方法,包括热量限制,包括限时喂养、间歇性禁食、禁食模拟饮食(FMD)和营养限制,特别是生酮饮食。尽管有很有前景的结果,但许多关于饮食限制的知识来自于体外和动物研究,这些研究可能无法准确反映现实生活中的情况。需要进一步研究以确定不同癌症和治疗方法的饮食限制的最佳持续时间、时间、安全性和疗效。此外,还需要精心设计的人体试验来建立特定代谢脆弱性与靶向饮食干预之间的联系。然而,临床试验中患者的低依从性仍然是一个重大挑战。