Department of Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna, Austria.
Leuk Res. 2013 Jun;37(6):631-6. doi: 10.1016/j.leukres.2013.02.008. Epub 2013 Mar 7.
In chronic lymphocytic leukaemia (CLL), lipoprotein lipase (LPL) mRNA overexpression is an established poor prognostic marker, its function, however, is poorly understood. Measuring extracellular LPL enzymatic activity and protein, we found no difference between levels in CLL patients and those of controls, both before and after heparin treatment in vivo and in vitro. Investigating LPL knock down effects, we determined five potential downstream targets, of which one gene, STXBP3, reportedly is involved in fatty acid metabolism. While possibly reflecting an epigenetic switch towards an incorrect transcriptional program, LPL overexpression by itself does not appear to significantly influence CLL cell survival.
在慢性淋巴细胞白血病(CLL)中,脂蛋白脂肪酶(LPL)mRNA 过表达是一个既定的预后不良标志物,但它的功能尚未得到很好的理解。我们测量了细胞外 LPL 的酶活性和蛋白,发现 CLL 患者与对照组患者之间在体内和体外肝素治疗前后均无差异。在研究 LPL 敲低的效果时,我们确定了五个潜在的下游靶标,其中一个基因 STXBP3 据称参与脂肪酸代谢。虽然这可能反映了向错误转录程序的表观遗传开关,但 LPL 的过表达本身似乎并没有显著影响 CLL 细胞的存活。