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血管紧张素II 1型拮抗剂通过抑制肿瘤血管生成来预防小鼠肾癌的肺转移。

Angiotensin II type I antagonist prevents pulmonary metastasis of murine renal cancer by inhibiting tumor angiogenesis.

作者信息

Miyajima Akira, Kosaka Takeo, Asano Tomohiko, Asano Takako, Seta Kaori, Kawai Toshiaki, Hayakawa Masamichi

机构信息

Department of Urology, National Defense Medical College, Tokorozawa, Saitama 359-8513, Japan.

出版信息

Cancer Res. 2002 Aug 1;62(15):4176-9.

Abstract

Angiotensin II (AII) is a potent vasoconstrictor peptide from the renin-angiotensin system in the kidney. The AII type 1 receptor (AT1R) is reportedly expressed in several tumors including renal cell carcinoma, and AII is involved in tumor angiogenesis. We p.o. administered the long-acting AT1R antagonist, candesartan (10 mg/kg), to the 16 days mouse renal cancer lung metastasis model to test the preventive effects in tumor metastasis. Pulmonary metastases of renal cancer showed prominent AT1R expression in both mice and humans, and candesartan treatment dramatically prevented lung metastatic nodules (14.9 +/- 1.8; P < 0.0001; n = 12) in mice along with the inhibition of neovascularization and vascular endothelial growth factor expression, compared with control metastatic mice (123.3 +/- 8.6; n = 13). Candesartan is widely used clinically, so it seems to be a reasonable therapy for patients with lung metastases of renal cell carcinoma.

摘要

血管紧张素II(AII)是一种来自肾脏肾素-血管紧张素系统的强效血管收缩肽。据报道,1型血管紧张素II受体(AT1R)在包括肾细胞癌在内的多种肿瘤中表达,且AII参与肿瘤血管生成。我们对16日龄的小鼠肾癌肺转移模型口服给予长效AT1R拮抗剂坎地沙坦(10毫克/千克),以测试其对肿瘤转移的预防作用。肾癌的肺转移在小鼠和人类中均显示出显著的AT1R表达,与对照转移性小鼠(123.3±8.6;n = 13)相比,坎地沙坦治疗显著减少了小鼠的肺转移结节(14.9±1.8;P < 0.0001;n = 12),同时抑制了新血管形成和血管内皮生长因子表达。坎地沙坦在临床上广泛使用,因此它似乎是肾细胞癌肺转移患者的一种合理治疗方法。

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