Mass spectrometric investigations of caloric restriction mimetics

被引:3
|
作者
Bibyk, Michael J. [1 ]
Campbell, Melanie J. [2 ]
Hummon, Amanda B. [1 ,2 ,3 ]
机构
[1] Ohio State Univ, Ohio State Biochem Program, Columbus, OH 43210 USA
[2] Ohio State Univ, Dept Chem & Biochem, Columbus, OH 43210 USA
[3] Ohio State Univ, Ctr Comprehens Canc, Columbus, OH 43210 USA
关键词
anti‐ cancer; caloric restriction; caloric restriction mimetic; hydroxycitric acid; mass spectrometry; proteomics; rapamycin; resveratrol; TOP-DOWN PROTEOMICS; MAMMALIAN TARGET; PROTEIN-ANALYSIS; LIFE-SPAN; RAPAMYCIN; CANCER; NUTRIGENOMICS; RESVERATROL; AUTOPHAGY; EXPRESSION;
D O I
10.1002/pmic.202000121
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Caloric restriction (CR) is an innovative therapy used in tumor tissue and tumor model studies to promote cell death and decrease cell viability. Caloric restriction mimetics (CRMs) are a class of drugs that induce CR and starvation conditions within a cell. When used simultaneously with other chemotherapy agents, the effects are synergistic and effective at promoting tumor cell death. In this review, we discuss CRMs and their potential as cancer therapeutics. Firstly, we establish an overview of CR and its impacts on healthy and tumor cells. CR and CRM drugs have shown to decrease age-related diseases and can act as an anti-cancer agent. As it can be challenging for an individual to diligently stick to a diet that would induce CR, CRMs are even more desirable. Then, we discuss the drug class by highlighting three CRMs: resveratrol, (-)-hydroxycitric acid, and rapamycin. These CRMs are commonly known for their dietary effects, but the underlying mechanisms that drive cellular metabolic and proteomic changes show promise as a cancer therapeutic. Lastly, we highlight the use of mass spectrometry and proteomic techniques on experiments utilizing CRM drugs to understand the cellular pathways impacted by this drug class, leading to a better understanding of the anti-cancer properties and potentials of CRM.
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页数:11
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