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癌症中肥胖途径的分子靶向治疗。

Molecular targeting of obesity pathways in cancer.

作者信息

Surmacz Eva, Otvos Laszlo

出版信息

Horm Mol Biol Clin Investig. 2015 May;22(2):53-62. doi: 10.1515/hmbci-2015-0007.

Abstract

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 downregulation, 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.

摘要

肥胖是多种癌症发生发展的重要风险因素,与肿瘤治疗反应较差以及肿瘤疾病早期复发有关。虽然这些关联的分子机制仍在研究中,但两种主要的脂肪组织来源的脂肪因子——瘦素和脂联素的功能失调似乎起着重要作用。已知瘦素可激活致癌途径,而脂联素似乎具有抗肿瘤活性并干扰瘦素诱导的过程。由于体内脂肪过多与瘦素表达增加和脂联素下调有关,对这些途径进行治疗性重新平衡可能使癌症患者受益,尤其是肥胖亚群。本综述重点关注我们设计的新型瘦素受体拮抗剂和脂联素受体激动剂,用于治疗性调节癌症中与肥胖相关的途径。

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