INSERM, U982, DC2N, IFRMP23, University of Rouen, Mont-Saint-Aignan, France.
Cell Mol Neurobiol. 2010 Nov;30(8):1383-9. doi: 10.1007/s10571-010-9594-9. Epub 2010 Nov 3.
Pheochromocytomas are catecholamine-producing tumors arising from chromaffin cells of the adrenal medulla or extra-adrenal location. Along with catecholamines, tumoral cells produce and secrete elevated quantities of trophic peptides which are normally released in a regulated manner by the normal adrenal medulla. Among these peptides, the amounts of pituitary adenylate cyclase-activating polypeptide (PACAP), adrenomedullin (AM), and neuropeptide Y (NPY) are particularly high. These peptides can exert endocrine, paracrine or autocrine effects in numerous cell types. In particular, they have been shown to be involved in cell proliferation and survival, catecholamine production and secretion, and angiogenesis. Some of these processes are exacerbated in pheochromocytomas, raising the possibility of the involvement of trophic peptides. Here, we review the expression levels of NPY, PACAP, and AM and theirs receptors in chromaffin cells and pheochromocytomas, and address their possible implication in the adrenal medulla tumorigenesis and malignant development of pheochromocytomas.
嗜铬细胞瘤是起源于肾上腺髓质或肾上腺外部位嗜铬细胞的儿茶酚胺产生肿瘤。与儿茶酚胺一起,肿瘤细胞产生和分泌大量的营养肽,这些肽通常由正常肾上腺髓质以调节的方式释放。在这些肽中,垂体腺苷酸环化酶激活肽(PACAP)、肾上腺髓质素(AM)和神经肽 Y(NPY)的含量特别高。这些肽可以在许多细胞类型中发挥内分泌、旁分泌或自分泌作用。特别是,它们已被证明参与细胞增殖和存活、儿茶酚胺的产生和分泌以及血管生成。这些过程中的一些在嗜铬细胞瘤中加剧,增加了营养肽参与的可能性。在这里,我们综述了 NPY、PACAP 和 AM 及其受体在嗜铬细胞和嗜铬细胞瘤中的表达水平,并探讨了它们在肾上腺髓质肿瘤发生和嗜铬细胞瘤恶性发展中的可能作用。