Faria Jerusa Araújo Quintão Arantes, Corrêa Natássia Caroline Resende, de Andrade Carolina, de Angelis Campos Ana Carolina, Dos Santos Samuel de Almeida Rubens, Rodrigues Thiago Souza, de Goes Alfredo Miranda, Gomes Dawidson Assis, Silva Fábio Pittella
Department of Biochemistry and Immunology, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, MG, Brazil.
Laboratory of Molecular Pathology of cancer, Faculty of Health Sciences, University of Brasília (UnB), Brasília, DF, Brazil.
J Cancer Sci Ther. 2013 Jan 21;5(2):58-65.
Cancer is comprised of a multitude of epigenetic abnormalities, including the global loss and regional gain of DNA methylation as well as alterations in histone methylation. Here, we characterize a new methyltransferase, SET domain-containing protein 4 (SETD4), which is involved in breast carcinogenesis. Quantitative real-time PCR (qPCR) showed elevated expression levels of SETD4 in several breast cancer cell lines. SETD4 overexpression was confirmed by western blot analysis suggesting a correlation between high expression of SETD4 and a lack of the estrogen receptor (ER) in breast cancer. In addition, cell fractionation studies and confocal immunofluorescence revealed the nuclear and non-nuclear localization of this new protein. SETD4 knockdown in breast cancer cell lines significantly suppressed their proliferation and delayed the G1/S cell cycle transition without affecting apoptosis. Furthermore, western blot analysis showed that knockdown of SETD4 decreased cyclin D1 expression, revealing the involvement of SETD4 in cell cycle regulation. These data imply that SETD4 plays a crucial role in breast carcinogenesis and could be a novel molecular target for the development of new strategies for the diagnosis and treatment of breast cancer.
癌症由多种表观遗传异常组成,包括DNA甲基化的整体缺失和局部增加以及组蛋白甲基化的改变。在此,我们鉴定了一种新的甲基转移酶,含SET结构域蛋白4(SETD4),其参与乳腺癌的发生。定量实时PCR(qPCR)显示SETD4在几种乳腺癌细胞系中的表达水平升高。蛋白质免疫印迹分析证实了SETD4的过表达,提示SETD4的高表达与乳腺癌中雌激素受体(ER)的缺失之间存在相关性。此外,细胞分级分离研究和共聚焦免疫荧光揭示了这种新蛋白的核定位和非核定位。乳腺癌细胞系中SETD4的敲低显著抑制了它们的增殖,并延迟了G1/S细胞周期转换,而不影响细胞凋亡。此外,蛋白质免疫印迹分析表明,SETD4的敲低降低了细胞周期蛋白D1的表达,揭示了SETD4参与细胞周期调控。这些数据表明,SETD4在乳腺癌发生中起关键作用,可能是开发乳腺癌诊断和治疗新策略的新型分子靶点。