Körner Meike, Reubi Jean Claude
Division of Cell Biology and Experimental Cancer Research, Institute of Pathology, University of Bern, Murtenstrasse 31, PO Box 62, CH-3010 Bern, Switzerland.
Peptides. 2007 Feb;28(2):419-25. doi: 10.1016/j.peptides.2006.08.037. Epub 2007 Jan 16.
Many peptide hormone receptors are over-expressed in human cancer, permitting an in vivo targeting of tumors for diagnostic and therapeutic purposes. NPY receptors are novel and promising candidates in this field. Using in vitro receptor autoradiography, Y1 and Y2 receptors have been found to be expressed in breast carcinomas, adrenal gland and related tumors, renal cell carcinomas, and ovarian cancers in both tumor cells and tumor-associated blood vessels. Pathophysiologically, tumoral NPY receptors may be activated by endogenous NPY released from intratumoral nerve fibers or tumor cells themselves, and mediate NPY effects on tumor cell proliferation and tumoral blood supply. Clinically, tumoral NPY receptors may be targeted with NPY analogs coupled with adequate radionuclides or cytotoxic agents for a scintigraphic tumor imaging and/or tumor therapy.
许多肽类激素受体在人类癌症中过度表达,这使得肿瘤能够在体内被靶向用于诊断和治疗目的。神经肽Y(NPY)受体是该领域中新型且有前景的候选者。通过体外受体放射自显影技术,已发现Y1和Y2受体在乳腺癌、肾上腺及相关肿瘤、肾细胞癌以及卵巢癌的肿瘤细胞和肿瘤相关血管中均有表达。在病理生理学上,肿瘤NPY受体可能被肿瘤内神经纤维或肿瘤细胞自身释放的内源性NPY激活,并介导NPY对肿瘤细胞增殖和肿瘤血液供应的影响。临床上,肿瘤NPY受体可以用与适当放射性核素或细胞毒性药物偶联的NPY类似物进行靶向,用于闪烁肿瘤成像和/或肿瘤治疗。