研究乳腺癌细胞中血管紧张素II AT2受体功能的新细胞模型。

International Journal of Peptides Pub Date : 2012-01-01 Epub Date: 2011-12-06 DOI:10.1155/2012/745027
Sylvie Rodrigues-Ferreira, Marina Morel, Rosana I Reis, Françoise Cormier, Véronique Baud, Claudio M Costa-Neto, Clara Nahmias
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引用次数: 9

摘要

最近的研究强调了AT1受体作为乳腺癌的潜在治疗靶点,而AT2亚型在该疾病中的作用在很大程度上仍然被忽视。本研究描述了一种新的人类浸润性乳腺癌细胞模型(D3H2LN-AT2)的产生和表征,该模型稳定表达高水平的flag标记的人类AT2受体(Flag-hAT2)。这些细胞表现出对AngII的高亲和力结合位点,并且总结合可以被at2选择性拮抗剂PD123319取代,但不能被at1选择性拮抗剂氯沙坦取代。有趣的是,荧光素酶和绿色荧光蛋白的高水平表达使这些细胞适合于体外和体内的生物发光和荧光研究。我们在这里提供了一种新的工具来研究乳腺癌细胞中AT2受体的功能,独立于AT1受体的激活。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Novel Cellular Model to Study Angiotensin II AT2 Receptor Function in Breast Cancer Cells.

A Novel Cellular Model to Study Angiotensin II AT2 Receptor Function in Breast Cancer Cells.

A Novel Cellular Model to Study Angiotensin II AT2 Receptor Function in Breast Cancer Cells.

A Novel Cellular Model to Study Angiotensin II AT2 Receptor Function in Breast Cancer Cells.

Recent studies have highlighted the AT1 receptor as a potential therapeutic target in breast cancer, while the role of the AT2 subtype in this disease has remained largely neglected. The present study describes the generation and characterization of a new cellular model of human invasive breast cancer cells (D3H2LN-AT2) stably expressing high levels of Flag-tagged human AT2 receptor (Flag-hAT2). These cells exhibit high-affinity binding sites for AngII, and total binding can be displaced by the AT2-selective antagonist PD123319 but not by the AT1-selective antagonist losartan. Of interest, high levels of expression of luciferase and green fluorescent protein make these cells suitable for bioluminescence and fluorescence studies in vitro and in vivo. We provide here a novel tool to investigate the AT2 receptor functions in breast cancer cells, independently of AT1 receptor activation.

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