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酒精通过激活血管内皮生长因子(VEGF)依赖的肿瘤血管生成来促进乳腺肿瘤生长。

Alcohol promotes mammary tumor growth through activation of VEGF-dependent tumor angiogenesis.

作者信息

Lu Yanmin, Ni Fang, Xu Mei, Yang Jinlian, Chen Ji, Chen Zhuo, Wang Xinyi, Luo Jia, Wang Siying

机构信息

Department of Pathophysiology, Anhui Medical University, Hefei, Anhui 230032, P.R. China ; Department of Hepatobiliary Surgery, Clinical Nutrition Center, Clinical Nutrition and Metabolism Key Laboratory, Binzhou Medical University Hospital, Binzhou, Shandong 256603, P.R. China.

Department of Pathophysiology, Anhui Medical University, Hefei, Anhui 230032, P.R. China.

出版信息

Oncol Lett. 2014 Aug;8(2):673-678. doi: 10.3892/ol.2014.2146. Epub 2014 May 16.

Abstract

Alcohol consumption has been recognized as a risk factor for breast cancer. Experimental studies demonstrate that alcohol exposure promotes the progression of existing mammary tumors. However, the mechanisms underlying this effect remain unclear. In the present study, the role of vascular endothelial growth factor (VEGF) in alcohol promotion of breast cancer development was investigated using a mouse xenograft model of mammary tumors and a three-dimensional (3D) tumor/endothelial cell co-culture system. For the mouse xenograft model, mouse E0771 breast cancer cells were implanted into the mammary fat pad of C57BL6 mice. These mice were exposed to alcohol in their drinking water. For the 3D co-culture system, E0771 cells and MDA-MB231 breast cancer cells were co-cultured with SVEC4-10EE2 and human umbilical vein endothelial cells, respectively. The results demonstrated that alcohol increased tumor angiogenesis and accelerated tumor growth. Furthermore, it appeared that alcohol induced VEGF expression in breast cancer cells and . Blocking VEGF signaling by SU5416 inhibited tumor angiogenesis in the 3D tumor/endothelial cell co-culture system. Furthermore, injection of SU5416 into mice inhibited alcohol-promoted mammary tumor growth . These results indicate that alcohol may promote mammary tumor growth by stimulating VEGF-dependent angiogenesis.

摘要

饮酒已被公认为是乳腺癌的一个风险因素。实验研究表明,酒精暴露会促进现有乳腺肿瘤的进展。然而,这种作用背后的机制仍不清楚。在本研究中,利用乳腺肿瘤的小鼠异种移植模型和三维(3D)肿瘤/内皮细胞共培养系统,研究了血管内皮生长因子(VEGF)在酒精促进乳腺癌发展中的作用。对于小鼠异种移植模型,将小鼠E0771乳腺癌细胞植入C57BL6小鼠的乳腺脂肪垫中。这些小鼠饮用含酒精的水。对于3D共培养系统,E0771细胞和MDA-MB231乳腺癌细胞分别与SVEC4-10EE2细胞和人脐静脉内皮细胞共培养。结果表明,酒精增加了肿瘤血管生成并加速了肿瘤生长。此外,酒精似乎诱导了乳腺癌细胞中VEGF的表达 。用SU5416阻断VEGF信号传导可抑制3D肿瘤/内皮细胞共培养系统中的肿瘤血管生成。此外,向小鼠注射SU5416可抑制酒精促进的乳腺肿瘤生长 。这些结果表明,酒精可能通过刺激VEGF依赖性血管生成来促进乳腺肿瘤生长。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa32/4081417/c1f361837d13/OL-08-02-0673-g00.jpg

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