Wong Sunny Y, Haack Herbert, Kissil Joseph L, Barry Marc, Bronson Roderick T, Shen Steven S, Whittaker Charles A, Crowley Denise, Hynes Richard O
Howard Hughes Medical Institute, Massachusetts Institute of Technology Center for Cancer Research, Cambridge, MA 02139, USA.
Proc Natl Acad Sci U S A. 2007 Jul 31;104(31):12784-9. doi: 10.1073/pnas.0705499104. Epub 2007 Jul 18.
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.
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。