Molecular targeting of obesity pathways in cancer

被引:14
作者
Surmacz, Eva [1 ]
Otvos, Laszlo [2 ]
机构
[1] Temple Univ, Sbarro Inst Canc Res & Mol Med, Philadelphia, PA 19122 USA
[2] Temple Univ, Dept Biol, Coll Sci & Technol, Philadelphia, PA 19122 USA
关键词
adipokines; adiponectin; cancer; leptin; metabolic signaling; peptide drugs; preclinical drug development;
D O I
10.1515/hmbci-2015-0007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Obesity is a significant risk factor for the development of different cancer types and has been associated with poorer response to oncotherapies and linked to earlier recurrence of the neoplastic disease. While molecular mechanisms of these associations are still under investigation, functional dysregulation of two major fat tissue-derived adipokines, leptin and adiponectin, appears to play an important role. Leptin is known to activate carcinogenic pathways, while adiponectin appears to exert antineoplastic activities and interfere with leptin-induced processes. Because excess body fat is associated with increased leptin expression and adiponectin down-regulation, therapeutic rebalancing of these pathways may benefit cancer patients, especially the obese subpopulations. This review focuses on our novel leptin receptor antagonists and adiponectin receptor agonists designed for therapeutic modulation of obesity-associated pathways in cancer.
引用
收藏
页码:53 / 62
页数:10
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