CR-UK Cambridge Research Institute, Li Ka Shing Centre, Cambridge CB2 0RE, UK.
EMBO Mol Med. 2010 Jan;2(1):16-25. doi: 10.1002/emmm.200900047.
Myc is activated in many tumours, yet, paradoxically, stimulates differentiation in mammalian epidermis. To test whether the epidermis responds differently to different levels of Myc, we treated K14MycER transgenic mice with a range of concentrations of the inducing agent, 4-hydroxy-tamoxifen (4OHT). Proliferation was stimulated at all levels of Myc activity; sebocyte differentiation was stimulated at low and intermediate levels; and interfollicular epidermal differentiation at intermediate and high levels. Mutational inactivation of the Myc p21 activated kinase 2 (PAK2) phosphorylation sites increased Myc activity and further enhanced epidermal differentiation. We conclude that Myc induced differentiation acts as a fail-safe device to prevent uncontrolled proliferation and neoplastic conversion of epidermal stem cells expressing high levels of Myc.
Myc 在许多肿瘤中被激活,但矛盾的是,它能刺激哺乳动物表皮的分化。为了测试表皮是否对不同水平的 Myc 有不同的反应,我们用一系列浓度的诱导剂 4-羟基他莫昔芬(4OHT)处理 K14MycER 转基因小鼠。增殖在 Myc 活性的所有水平都受到刺激;在低和中等水平下刺激皮脂细胞分化;在中等和高水平下刺激毛囊间表皮分化。Myc 激活的 p21 激活激酶 2(PAK2)磷酸化位点的突变失活增加了 Myc 的活性,并进一步增强了表皮分化。我们得出结论,Myc 诱导的分化作为一种失效保护装置,防止高水平表达 Myc 的表皮干细胞不受控制的增殖和肿瘤转化。