Godin-Heymann N, Brabetz S, Murillo M M, Saponaro M, Santos C R, Lobley A, East P, Chakravarty P, Matthews N, Kelly G, Jordan S, Castellano E, Downward J
Signal Transduction, Cancer Research UK London Research Institute, London, UK.
The Institute of Cancer Research, London, UK.
Oncogene. 2016 Jun 23;35(25):3324-34. doi: 10.1038/onc.2015.394. Epub 2015 Oct 12.
Suppression of detachment-induced cell death, known as anoikis, is an essential step for cancer metastasis to occur. We report here that expression of KLF12, a member of the Kruppel-like family of transcription factors, is downregulated in lung cancer cell lines that have been selected to grow in the absence of cell adhesion. Knockdown of KLF12 in parental cells results in decreased apoptosis following cell detachment from matrix. KLF12 regulates anoikis by promoting the cell cycle transition through S phase and therefore cell proliferation. Reduced expression levels of KLF12 results in increased ability of lung cancer cells to form tumours in vivo and is associated with poorer survival in lung cancer patients. We therefore identify KLF12 as a novel metastasis-suppressor gene whose loss of function is associated with anoikis resistance through control of the cell cycle.
抑制脱离诱导的细胞死亡(即失巢凋亡)是癌症发生转移的关键步骤。我们在此报告,Kruppel样转录因子家族成员KLF12在已被选择在无细胞黏附条件下生长的肺癌细胞系中表达下调。在亲代细胞中敲低KLF12会导致细胞从基质脱离后凋亡减少。KLF12通过促进细胞周期通过S期进而促进细胞增殖来调节失巢凋亡。KLF12表达水平降低会导致肺癌细胞在体内形成肿瘤的能力增强,且与肺癌患者较差的生存率相关。因此,我们将KLF12鉴定为一种新型的转移抑制基因,其功能丧失通过控制细胞周期与失巢凋亡抗性相关。