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尾加压素Ⅱ及其受体在人肾透明细胞癌组织中的表达及意义 被引量:1

Expression of Urotensin Ⅱ and its Receptor in Human Renal Clear Cell Carcinoma Tissues
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摘要 目的:测定肾透明细胞癌中尾加压素Ⅱ(UⅡ)与其受体(UT-R)的表达量,以期探讨UⅡ与UT-R的表达在肾透明细胞癌发生中的临床意义。方法:对12例肾透明细胞癌肿瘤组织通过免疫组化检测肾透明细胞癌组织和正常肾组织UⅡ蛋白的表达,并采用逆转录-多聚酶链式反应(RT PCR)的方法测定肾透明细胞癌组织和正常肾组织UⅡmRNA和UT-RmRNA的表达量。结果:肾透明细胞癌组织和正常肾组织中有UⅡ蛋白表达。RT-PCR结果显示肾透明细胞癌中UⅡmRNA的表达明显高于正常肾组织0.92±0.09和0.62±0.06(P<0.01)。UT-R mRNA的表达明显高于正常肾组织0.28±0.01和0.16±0.03(P<0.01)。结论:肾透明细胞癌中UⅡ和UT-RmRNA高表达提示UⅡ/UT系统可能与肾透明细胞癌的发生、发展有关,UⅡ可能通过自分泌或旁分泌的方式发挥作用。 Objective:To examine the expression of U Ⅱ and UT-R in human renal clear cell carcinoma tissues and attached non neoplastic renal tissues in order to assess a possible autocrine/paracrine role of U Ⅱ in renal tumors. Methods: Twelve renal clear cell carcinoma tissues and normal renal tissues were obtained from patients received radical nephrectomy. U Ⅱ protein was measured by immunohistochemistry, and U Ⅱ mRNA and UT-R mRNA expression was analyzed by RT-PCR. Results:Renal clear cell carcinoma and normal kidney protein expression in U Ⅱ. RT - PCR results showed that renal cell carcinoma U Ⅱ mRNA was significantly higher than normal kidney tissue0. 92 ± 0.09 and0. 62 ± 0.06 ( P d0.01). UT- R mRNA expression was significantly higher than normal kidney tissue 0 . 28 ± 0 . 01 and 0 . 16 ±0 . 03 ( P 〈0 . 01). Conelusions..The overexpression of U Ⅱ and UT RmRNA in renal clear cell carcinoma of U Ⅱ and UT RmRNA overexpression of U Ⅱ/UT system may indicate UⅡ / UT system is associated with renal clear cell carcinoma, UⅡ may play a role through the autocrine or paracrine manner. Key words
出处 《临床泌尿外科杂志》 北大核心 2010年第7期510-513,共4页 Journal of Clinical Urology
关键词 肾肿瘤 透明细胞癌 尾加压素Ⅱ Urotensin Ⅱ renal carcinoma clear cell carcinoma
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参考文献7

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  • 1吴登龙,王文静,关明,金三宝,金重睿,张元芳.表面增强激光解吸/离子化质谱蛋白质芯片技术在筛选肾癌患者尿液标记物中的应用[J].中华医学杂志,2004,84(13):1092-1095. 被引量:22
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  • 4BOSSO N, CHINELLO C, PICOZZI SCM, et al. Human urine biomarkers of renal cell carcinoma evaluated by ClinProt[J]. Prot Clin Appli, 2(}08, 2 (7-8) : 1036-1046.
  • 5FRANTZIA M, METZGERA J, BANKSC RE, et al. Discovery and validation of urinary biomarkers for detection of renal cell carcinoma[J]. J Prot, 2014, 98: 44-58.
  • 6YOSHIMOTO T, MIKA MATSUSHITA, HIRATA Y. Role of urotensin II in peripheral tissue as an autocrine/paracrine growth facto[J]. Peptides, 2004, 25 (10): 1775-1781.
  • 7HEUSER M, SCHLOTT T, SCHALLY A, et al. Expression of gastrin releasing peptide receptor in renal cell carcinomas: a potential function for the regulation of neoangiogenesis and mi- crovascular perfusion[J]. J Urol, 2005, 173 (6): 2154-2159.
  • 8ANSKY A, WEERTH AD, FASLER-KAN E, et al. Gastrin releasing peptide-preferring bombesin receptors mediate growth of human renal cell carcinoma[J]. J Amer Soci Nephrol, 2000, 11 (8):1409-1418.
  • 9ISCHIA J, PATEL O, SETHI K, et al. Identification of bind- ing sites for C-terminal pro-gastrin-releasing peptide (GRP)-de- rived peptides in renal cell carcinoma: a potential target for fu- ture therapy[J]. Bri J Urol Int, 2015, 115(5):829-838.
  • 10MODLIN M, GUSTAFSSON B, MOSSS, et al. Chromogranin a-biological function and clinical utility in neuro endocrine tumor disease [J]. Ann Surg Oncol, 2010, 17 (9): 2427-2443.

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