Department of Biology, West Virginia State University, Institute, WV, USA.
Adv Neurobiol. 2024;35:45-85. doi: 10.1007/978-3-031-45493-6_4.
It has become apparent that endogenous opioids act not only as neurotransmitters and neuromodulators, but have multiple functions in the body. Activation of the opioid system by opiate drugs is associated with a risk of cancer development through direct stimulation of tumor cell proliferation and through immunosuppression. In contrast, the endogenous peptide opioid [Met]-enkephalin, now commonly referred to as Opioid Growth Factor (OGF), negatively regulates cell proliferation in a wide number of cells during development, homeostasis, and neoplasia. This action is mediated through the opioid growth factor receptor, originally designated the zeta (ζ) opioid receptor. Further, contrary to the traditional notion of opiates as immunosuppressive, endogenous OGF has been shown to possess a number of positive immunomodulatory properties and may provide a beneficial effect in cancer by augmenting the activity of cells involved in both innate and acquired immunity. Taken together, the evidence supports consideration of opioid peptides such as OGF as new strategies for cancer therapy.
很明显,内源性阿片肽不仅作为神经递质和神经调质起作用,而且在体内具有多种功能。阿片类药物通过激活阿片系统与癌症发展的风险相关,这是通过直接刺激肿瘤细胞增殖和免疫抑制来实现的。相比之下,内源性肽阿片[Met]-脑啡肽,现在通常被称为阿片生长因子(OGF),在发育、稳态和肿瘤发生过程中,对多种细胞的增殖具有负调节作用。这种作用是通过阿片生长因子受体介导的,该受体最初被指定为ζ(ζ)阿片受体。此外,与阿片类药物作为免疫抑制药物的传统观念相反,内源性 OGF 已被证明具有许多积极的免疫调节特性,并可通过增强参与固有和获得性免疫的细胞的活性,在癌症中提供有益的效果。综上所述,这些证据支持将阿片肽(如 OGF)视为癌症治疗的新策略。