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蛋白质4.1B可抑制前列腺癌的进展和转移。

Protein 4.1B suppresses prostate cancer progression and metastasis.

作者信息

Wong Sunny Y, Haack Herbert, Kissil Joseph L, Barry Marc, Bronson Roderick T, Shen Steven S, Whittaker Charles A, Crowley Denise, Hynes Richard O

机构信息

Howard Hughes Medical Institute, Massachusetts Institute of Technology Center for Cancer Research, Cambridge, MA 02139, USA.

出版信息

Proc Natl Acad Sci U S A. 2007 Jul 31;104(31):12784-9. doi: 10.1073/pnas.0705499104. Epub 2007 Jul 18.

Abstract

Protein 4.1B is a 4.1/ezrin/radixin/moesin domain-containing protein whose expression is frequently lost in a variety of human tumors, including meningiomas, non-small-cell lung cancers, and breast carcinomas. However, its potential tumor-suppressive function under in vivo conditions remains to be validated. In a screen for genes involved with prostate cancer metastasis, we found that 4.1B expression is reduced in highly metastatic tumors. Down-regulation of 4.1B increased the metastatic propensity of poorly metastatic cells in an orthotopic model of prostate cancer. Furthermore, 4.1B-deficient mice displayed increased susceptibility for developing aggressive, spontaneous prostate carcinomas. In both cases, enhanced tumor malignancy was associated with reduced apoptosis. Because expression of Protein 4.1B is frequently down-regulated in human clinical prostate cancer, as well as in a spectrum of other tumor types, these results suggest a more general role for Protein 4.1B as a negative regulator of cancer progression to metastatic disease.

摘要

蛋白质4.1B是一种含有4.1/埃兹蛋白/根蛋白/膜突蛋白结构域的蛋白质,其表达在包括脑膜瘤、非小细胞肺癌和乳腺癌在内的多种人类肿瘤中经常缺失。然而,其在体内条件下的潜在肿瘤抑制功能仍有待验证。在一项针对与前列腺癌转移相关基因的筛选中,我们发现4.1B在高转移性肿瘤中的表达降低。在前列腺癌原位模型中,4.1B的下调增加了低转移性细胞的转移倾向。此外,缺乏4.1B的小鼠对侵袭性自发性前列腺癌的易感性增加。在这两种情况下,肿瘤恶性程度的增强都与细胞凋亡减少有关。由于蛋白质4.1B的表达在人类临床前列腺癌以及一系列其他肿瘤类型中经常下调,这些结果表明蛋白质4.1B作为癌症进展至转移性疾病的负调节因子具有更普遍的作用。

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