Harvey Amanda J, Crompton Mark R
School of Biological Sciences, Royal Holloway University of London, Egham, Surrey TW20 OEX, UK.
Oncogene. 2003 Aug 7;22(32):5006-10. doi: 10.1038/sj.onc.1206577.
Brk (PTK6) is a nonreceptor protein tyrosine kinase, which is expressed in over 60% of breast carcinoma tissue samples and breast tumour cell lines, but not normal mammary tissue or benign lesions. Since experimental Brk expression in nontransformed mammary epithelial cells enhances their mitogenic response to epidermal growth factor, it was important to determine the role Brk plays in the proliferation of breast carcinoma cells and validate it as a therapeutic target. We have used RNA interference to efficiently and specifically downregulate Brk protein levels in breast carcinoma cells, and determined that this results in a significant suppression of their proliferation. Additionally, through the expression of a kinase-inactive mutant, we have determined that Brk can mediate promotion of proliferation via a kinase-independent mechanism, potentially functioning as an 'adapter'. These data identify Brk as a novel target for antiproliferative therapy in the majority of breast cancers, and illustrate the power of RNA interference for rapidly validating candidate therapeutic targets.
Brk(PTK6)是一种非受体蛋白酪氨酸激酶,在超过60%的乳腺癌组织样本和乳腺肿瘤细胞系中表达,但在正常乳腺组织或良性病变中不表达。由于在未转化的乳腺上皮细胞中进行实验性Brk表达可增强其对表皮生长因子的促有丝分裂反应,因此确定Brk在乳腺癌细胞增殖中所起的作用并将其验证为治疗靶点很重要。我们利用RNA干扰有效且特异性地下调了乳腺癌细胞中Brk蛋白水平,并确定这会导致其增殖受到显著抑制。此外,通过表达一种激酶失活突变体,我们确定Brk可通过一种不依赖激酶的机制介导增殖促进作用,可能发挥“衔接子”的功能。这些数据确定Brk是大多数乳腺癌抗增殖治疗的新靶点,并说明了RNA干扰在快速验证候选治疗靶点方面的作用。