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WAP-TAg/WAP-maspin双转基因小鼠乳腺肿瘤进展减缓。

Reduced mammary tumor progression in WAP-TAg/WAP-maspin bitransgenic mice.

作者信息

Zhang M, Shi Y, Magit D, Furth P A, Sager R

机构信息

Department of Molecular & Cellular Biology, Baylor College of Medicine, Houston, Texas 77030, USA.

出版信息

Oncogene. 2000 Dec 7;19(52):6053-8. doi: 10.1038/sj.onc.1204006.

Abstract

Maspin is a unique serpin involved in the suppression of tumor growth and metastasis. To investigate whether increased levels of maspin protect against tumor progression in vivo, we established a transgenic model in which maspin is targeted to mammary epithelial cells by the Whey Acidic Protein (WAP) promoter for overexpression. We crossed these WAP-maspin transgenic mice with the WAP-TAg mouse model of tumor progression. Maspin overexpression increased the rate of apoptosis of both preneoplastic and carcinomatous mammary epithelial cells. Maspin reduced tumor growth through a combination of reduced angiogenesis and increased apoptosis. The number of pulmonary metastases was reduced in the presence of maspin overexpression. These data demonstrate that targeted overexpression of maspin can inhibit tumor progression in vivo, likely through a combination of increased apoptosis, decreased angiogenesis, and inhibition of tumor cell migration.

摘要

Maspin是一种独特的丝氨酸蛋白酶抑制剂,参与抑制肿瘤生长和转移。为了研究maspin水平升高是否能在体内预防肿瘤进展,我们建立了一种转基因模型,其中maspin通过乳清酸性蛋白(WAP)启动子靶向乳腺上皮细胞进行过表达。我们将这些WAP-maspin转基因小鼠与肿瘤进展的WAP-TAg小鼠模型进行杂交。Maspin过表达增加了癌前和癌性乳腺上皮细胞的凋亡率。Maspin通过减少血管生成和增加凋亡的组合来降低肿瘤生长。在maspin过表达的情况下,肺转移的数量减少。这些数据表明,maspin的靶向过表达可以在体内抑制肿瘤进展,可能是通过增加凋亡、减少血管生成和抑制肿瘤细胞迁移的组合来实现的。

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