Cyclic fasting-mimicking diet in cancer treatment: Preclinical and clinical evidence

被引:4
|
作者
Vernieri, Claudio [1 ,2 ]
Ligorio, Francesca [1 ,3 ]
Tripathy, Debu [4 ]
Longo, Valter D. [2 ,5 ,6 ]
机构
[1] Univ Milan, Med Oncol & Hematol Oncol Dept, I-20122 Milan, Italy
[2] AIRC Inst Mol Oncol, IFOM ETS, I-20139 Milan, Italy
[3] Fdn IRCCS Ist Nazl Tumori, Med Oncol Dept, I-20133 Milan, Italy
[4] Univ Texas MD Anderson Canc Ctr, Dept Breast Med Oncol, Unit 1354, 1515 Holcombe Blvd, Houston, TX 77030 USA
[5] Univ Southern Calif, Longev Inst, Davis Sch Gerontol, Los Angeles, CA 90089 USA
[6] Univ Southern Calif, Dept Biol Sci, Los Angeles, CA 90089 USA
基金
欧洲研究理事会;
关键词
NEGATIVE BREAST-CANCER; ASCORBIC-ACID; LUNG-CANCER; CELL-GROWTH; METABOLIC PLASTICITY; VITAMIN-C; GLUTAMINE; METHIONINE; APOPTOSIS; SURVIVAL;
D O I
10.1016/j.cmet.2024.06.014
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In preclinical tumor models, cyclic fasting and fasting-mimicking diets (FMDs) produce antitumor effects that become synergistic when combined with a wide range of standard anticancer treatments while protecting normal tissues from treatment-induced adverse events. More recently, results of phase 1/2 clinical trials showed that cyclic FMD is safe, feasible, and associated with positive metabolic and immunomodulatory effects in patients with different tumor types, thus paving the way for larger clinical trials to investigate FMD anticancer activity in different clinical contexts. Here, we review the tumor-cell-autonomous and immune-system-mediated mechanisms of fasting/FMD antitumor effects, and we critically discuss new metabolic interventions that could synergize with nutrient starvation to boost its anticancer activity and prevent or reverse tumor resistance while minimizing toxicity to patients. Finally, we highlight potential future applications of FMD approaches in combination with standard anticancer strategies as well as strategies to implement the design and conduction of clinical trials.
引用
收藏
页码:1644 / 1667
页数:24
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