Department of Gynecologic Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Unit 1362, 1515 Holcombe Blvd., Houston, TX, 77030, USA.
Department of Cancer Biology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Cancer Metastasis Rev. 2018 Sep;37(2-3):203-211. doi: 10.1007/s10555-018-9741-1.
Clinical and experimental studies support the notion that adrenergic stimulation and chronic stress affect inflammation, metabolism, and tumor growth. Eicosanoids are also known to heavily influence inflammation while regulating certain stress responses. However, additional work is needed to understand the full extent of interactions between the stress-related pathways and eicosanoids. Here, we review the potential influences that stress, inflammation, and metabolic pathways have on each other, in the context of eicosanoids. Understanding the intricacies of such interactions could provide insights on how systemic metabolic effects mediated by the stress pathways can be translated into therapies for cancer and other diseases.
临床和实验研究支持这样一种观点,即肾上腺素能刺激和慢性应激会影响炎症、代谢和肿瘤生长。人们还知道,类二十烷酸在调节某些应激反应的同时,也会强烈影响炎症。然而,需要做更多的工作来了解应激相关途径和类二十烷酸之间相互作用的全部范围。在这里,我们回顾了在类二十烷酸的背景下,应激、炎症和代谢途径相互之间可能产生的影响。了解这种相互作用的复杂性,可以深入了解由应激途径介导的全身代谢效应如何转化为癌症和其他疾病的治疗方法。