Couvineau Alain, Dayot Stéphanie, Nicole Pascal, Gratio Valérie, Rebours Vinciane, Couvelard Anne, Voisin Thierry
INSERM UMR1149/Inflammation Research Center (CRI), Team "From Inflammation to Cancer in Digestive Diseases" Labeled by "La Ligue Nationale Contre Le Cancer," Paris-Diderot University, DHU UNITY, Paris, France.
Front Endocrinol (Lausanne). 2018 Sep 27;9:573. doi: 10.3389/fendo.2018.00573. eCollection 2018.
Orexins (OxA and OxB) also termed hypocretins are hypothalamic neuropeptides involved in central nervous system (CNS) to control the sleep/wake process which is mediated by two G protein-coupled receptor subtypes, OX1R, and OX2R. Beside these central effects, orexins also play a role in various peripheral organs such as the intestine, pancreas, adrenal glands, kidney, adipose tissue and reproductive tract.In the past few years, an unexpected anti-tumoral role of orexins mediated by a new signaling pathway involving the presence of two immunoreceptor tyrosine-based inhibitory motifs (ITIM) in both orexin receptors subtypes, the recruitment of the phosphotyrosine phosphatase SHP2 and the induction of mitochondrial apoptosis has been elucidated. In the present review, we will discuss the anti-tumoral effect of orexin/OXR system in colon, pancreas, prostate and other cancers, and its interest as a possible therapeutic target.
食欲素(OxA和OxB),也被称为下丘脑泌素,是下丘脑神经肽,参与中枢神经系统(CNS)对睡眠/觉醒过程的控制,该过程由两种G蛋白偶联受体亚型OX1R和OX2R介导。除了这些中枢作用外,食欲素在各种外周器官中也发挥作用,如肠道、胰腺、肾上腺、肾脏、脂肪组织和生殖道。在过去几年中,食欲素通过一种新的信号通路发挥意想不到的抗肿瘤作用,该信号通路涉及两种食欲素受体亚型中均存在两个基于免疫受体酪氨酸的抑制基序(ITIM)、招募磷酸酪氨酸磷酸酶SHP2以及诱导线粒体凋亡。在本综述中,我们将讨论食欲素/OXR系统在结肠癌、胰腺癌和前列腺癌等癌症中的抗肿瘤作用,以及其作为潜在治疗靶点的意义。