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去甲肾上腺素上调鼻咽癌肿瘤细胞中血管内皮生长因子、基质金属蛋白酶(MMP)-2和MMP-9的表达。

Norepinephrine up-regulates the expression of vascular endothelial growth factor, matrix metalloproteinase (MMP)-2, and MMP-9 in nasopharyngeal carcinoma tumor cells.

作者信息

Yang Eric V, Sood Anil K, Chen Min, Li Yang, Eubank Tim D, Marsh Clay B, Jewell Scott, Flavahan Nicholas A, Morrison Carl, Yeh Peir-En, Lemeshow Stanley, Glaser Ronald

机构信息

Department of Molecular Virology, The Ohio State University Medical Center, Columbus, OH 43210, USA.

出版信息

Cancer Res. 2006 Nov 1;66(21):10357-64. doi: 10.1158/0008-5472.CAN-06-2496.

DOI:10.1158/0008-5472.CAN-06-2496
PMID:17079456
Abstract

Recent studies using ovarian cancer cells have shown that the catecholamine hormones norepinephrine (norepi) and epinephrine (epi) may influence cancer progression by modulating the expression of matrix metalloproteinases (MMP) and vascular endothelial growth factor (VEGF). The purpose of this study is to determine if the stress hormone norepi can influence the expression of MMP-2, MMP-9, and VEGF in nasopharyngeal carcinoma (NPC) tumors by using three NPC tumor cell lines. The NPC cell lines HONE-1, HNE-1, and CNE-1 were treated with norepi. The effects of norepi on MMP-2, MMP-9, and VEGF synthesis were measured by ELISA; functional MMP activity was measured by the invasive potential of the cells using a membrane invasion culture system whereas functional activity of VEGF was analyzed using a human umbilical vein endothelial cell tube formation assay. Norepi treatment increased MMP-2, MMP-9, and VEGF levels in culture supernatants of HONE-1 cells, which could be inhibited by the beta-blocker propranolol. Norepi induced the invasiveness of all NPC cell lines in a dose-dependent manner, which was blocked by CMT-3, an MMP inhibitor, and propranolol. Norepi stimulated the release of functional angiogenic VEGF by HONE-1 cells as well. Finally, HONE-1 cells were shown to express beta-adrenergic receptors as did seven of seven NPC biopsies examined. The data suggest that catecholamine hormones produced by the sympathetic-adrenal medullary axis may affect NPC tumor progression, in part, through modulation of key angiogenic cytokines.

摘要

最近使用卵巢癌细胞的研究表明,儿茶酚胺激素去甲肾上腺素(norepi)和肾上腺素(epi)可能通过调节基质金属蛋白酶(MMP)和血管内皮生长因子(VEGF)的表达来影响癌症进展。本研究的目的是通过使用三种鼻咽癌(NPC)肿瘤细胞系来确定应激激素去甲肾上腺素是否能影响NPC肿瘤中MMP-2、MMP-9和VEGF的表达。用去甲肾上腺素处理NPC细胞系HONE-1、HNE-1和CNE-1。通过酶联免疫吸附测定(ELISA)测量去甲肾上腺素对MMP-2、MMP-9和VEGF合成的影响;使用膜侵袭培养系统通过细胞的侵袭潜力测量功能性MMP活性,而使用人脐静脉内皮细胞管形成试验分析VEGF的功能活性。去甲肾上腺素处理增加了HONE-1细胞培养上清液中MMP-2、MMP-9和VEGF的水平,这可被β受体阻滞剂普萘洛尔抑制。去甲肾上腺素以剂量依赖性方式诱导所有NPC细胞系的侵袭性,这被MMP抑制剂CMT-3和普萘洛尔阻断。去甲肾上腺素也刺激HONE-1细胞释放功能性血管生成VEGF。最后,HONE-1细胞显示表达β-肾上腺素能受体,所检测的7例NPC活检组织中有7例也是如此。数据表明,交感-肾上腺髓质轴产生的儿茶酚胺激素可能部分通过调节关键的血管生成细胞因子来影响NPC肿瘤进展。

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