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瘦素和脂联素:乳腺癌治疗的新靶点。

Leptin and adiponectin: emerging therapeutic targets in breast cancer.

机构信息

Sbarro Institute for Cancer Research and Molecular Medicine, Temple University, 1900 N12th Street, BioLife Bldg. Rm 425, Philadelphia, PA, 19122, USA,

出版信息

J Mammary Gland Biol Neoplasia. 2013 Dec;18(3-4):321-32. doi: 10.1007/s10911-013-9302-8. Epub 2013 Oct 18.

Abstract

Obesity is a recognized risk factor for breast cancer development and poorer response to therapy. Two major fat tissue-derived adipokines, leptin and adiponectin have been implicated in mammary carcinogenesis. Leptin appears to promote breast cancer progression through activation of mitogenic, antiapoptotic, and metastatic pathways, while adiponectin may restrict tumorigenic processes primarily by inhibiting cell metabolism. Furthermore, adiponectin is known to counteract detrimental leptin effects in breast cancer models. Thus, therapeutic inhibition of pro-neoplastic leptin pathways and reactivation of anti-neoplastic adiponectin signaling may benefit breast cancer patients, especially the obese subpopulation. This review focuses on current experimental strategies aiming at leptin and adiponectin pathways in breast cancer models. Novel leptin receptor antagonists and adiponectin receptor agonists as well as other compounds for therapeutic modulation of adipokine pathways are discussed in detail, including potential pharmacological advantages and limitations of these approaches.

摘要

肥胖是乳腺癌发生和治疗反应较差的公认危险因素。两种主要的脂肪组织来源的脂肪因子,瘦素和脂联素,与乳腺癌的发生有关。瘦素似乎通过激活有丝分裂、抗凋亡和转移途径促进乳腺癌的进展,而脂联素可能主要通过抑制细胞代谢来限制肿瘤发生过程。此外,已知脂联素可以拮抗乳腺癌模型中的有害瘦素作用。因此,抑制致癌性的瘦素途径和重新激活抗肿瘤的脂联素信号可能使乳腺癌患者受益,尤其是肥胖亚群。这篇综述重点介绍了目前针对乳腺癌模型中瘦素和脂联素途径的实验策略。详细讨论了新型瘦素受体拮抗剂和脂联素受体激动剂以及其他用于治疗性调节脂肪因子途径的化合物,包括这些方法的潜在药理优势和局限性。

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