Boelens Jerina, Lust Sofie, Van Bockstaele Femke, Van Gele Mireille, Janssens Ann, Derycke Lara, Vanhoecke Barbara, Philippé Jan, Bracke Marc, Offner Fritz
Department of Hematology, Ghent University Hospital, Ghent, Belgium.
Leuk Res. 2009 Oct;33(10):1335-43. doi: 10.1016/j.leukres.2009.02.022. Epub 2009 Mar 17.
There is resurgent interest in glucocorticoids (GCs) in the treatment of poor prognosis chronic lymphocytic leukemia (CLL). Little is known however on how GCs induce apoptosis in CLL. Methylprednisolone (MP) induces apoptosis in ZAP-70 positive CLL more readily than in ZAP-70 negative CLL, which is in contrast to the effects of radiation and chemotherapy. The increased GC sensitivity of ZAP-70+ CLL was studied in relation to the expression status of ZAP-70 and the related signal transducing tyrosine kinase SYK. Both ZAP-70 and SYK were downregulated by GC treatment. Moreover, SYK was dephosphorylated by the phosphatase PTP1B of which the expression and translation levels were induced by GCs. Inhibition of PTP1B successfully restored ZAP-70 expression and SYK phosphorylation but did not interfere with GC-induced apoptosis. Therefore, the downregulation of ZAP-70 and P-SYK per se during treatment with GCs is not sufficient to induce apoptosis, and different mechanisms must therefore be responsible for the increased steroid sensitivity of ZAP-70+ CLL.
糖皮质激素(GCs)在治疗预后不良的慢性淋巴细胞白血病(CLL)方面重新引起了人们的关注。然而,关于GCs如何诱导CLL细胞凋亡,人们了解甚少。甲基泼尼松龙(MP)诱导ZAP-70阳性CLL细胞凋亡比诱导ZAP-70阴性CLL细胞凋亡更容易,这与放疗和化疗的效果相反。研究了ZAP-70 + CLL对GCs敏感性增加与ZAP-70及相关信号转导酪氨酸激酶SYK表达状态的关系。GC治疗可使ZAP-70和SYK均下调。此外,SYK被磷酸酶PTP1B去磷酸化,而PTP1B的表达和翻译水平由GCs诱导。抑制PTP1B成功恢复了ZAP-70表达和SYK磷酸化,但并未干扰GC诱导的细胞凋亡。因此,GC治疗期间ZAP-70和磷酸化SYK本身的下调不足以诱导细胞凋亡,因此必然有不同的机制导致ZAP-70 + CLL对类固醇敏感性增加。