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生长激素释放激素受体剪接变体1在原发性人类黑色素瘤中的表达

Expression of growth hormone-releasing hormone receptor splice variant 1 in primary human melanomas.

作者信息

Chatzistamou Ioulia, Volakaki Aspasia-Athina, Schally Andrew V, Kiaris Hippokratis, Kittas Christos

机构信息

Department of Histology and Embryology, Medical School, University of Athens, 75 Micras Asias, 115 27 Athens, Greece.

出版信息

Regul Pept. 2008 Apr 10;147(1-3):33-6. doi: 10.1016/j.regpep.2007.12.008. Epub 2008 Jan 11.

DOI:10.1016/j.regpep.2007.12.008
PMID:18255167
Abstract

Growth hormone-releasing hormone (GHRH) is secreted by the hypothalamus and upon binding to specific GHRH receptors in the pituitary stimulates growth hormone production and release. In addition to its neuroendocrine action GHRH plays a role in tumorigenesis. Consistently with this latter role, the splice variant 1 (SV1) of GHRH receptor, which is widely expressed in non-pituitary normal tissues and cancers, can mediate the proliferative effects of GHRH and even in the absence of GHRH is capable of eliciting mitogenic signals in the tissues in which it is expressed. The aim of the present study was to investigate the expression of GHRH and its tumoral receptor SV1 in primary human melanomas and dysplastic nevi by immunohistochemistry. None of the specimens tested expressed GHRH. Only 1 of 12 (8%) dysplastic nevi expressed SV1 but 14 of 23 (61%) melanomas showed moderate or strong staining for SV1 (association p<0.005). This is the first report demonstrating the involvement of SV1 in the pathogenesis of melanomas. Our work implies that the progression from a state of dysplasia into malignancy is accompanied by expression of SV1 receptor. Our findings also suggest that treatment with GHRH antagonists should be further explored for the management of malignant melanomas.

摘要

生长激素释放激素(GHRH)由下丘脑分泌,与垂体中的特定GHRH受体结合后,可刺激生长激素的产生和释放。除了其神经内分泌作用外,GHRH在肿瘤发生中也发挥作用。与后一种作用一致,GHRH受体的剪接变体1(SV1)在非垂体正常组织和癌症中广泛表达,它可以介导GHRH的增殖作用,甚至在没有GHRH的情况下,也能够在其表达的组织中引发有丝分裂信号。本研究的目的是通过免疫组织化学研究GHRH及其肿瘤受体SV1在原发性人类黑色素瘤和发育异常痣中的表达。所检测的标本均未表达GHRH。12个发育异常痣中只有1个(8%)表达SV1,但23个黑色素瘤中有14个(61%)对SV1呈中度或强染色(关联p<0.005)。这是第一份证明SV1参与黑色素瘤发病机制的报告。我们的研究表明,从发育异常状态发展为恶性肿瘤伴随着SV1受体的表达。我们的研究结果还表明,应进一步探索使用GHRH拮抗剂治疗恶性黑色素瘤。

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