Busiello Teresa, Ciano Michela, Romano Simona, Sodaro Gaetano, Garofalo Olgavalentina, Bruzzese Dario, Simeone Luigia, Chiurazzi Federico, Fiammetta Romano Maria, Costanzo Paola, Cesaro Elena
Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, Via Pansini 5 80131, Naples, Italy.
Department of Public Health, University of Naples Federico II, Via Pansini 5, 80131, Naples, Italy.
Hum Mol Genet. 2017 Jan 15;26(2):344-353. doi: 10.1093/hmg/ddw427.
Chronic lymphocytic leukaemia (CLL) is associated with apoptosis resistance and defective control of cell growth. Our study describes for the first time a critical role in CLL for the KRAB-zinc finger protein ZNF224. High ZNF224 transcript levels were detected in CLL patients with respect to control cells. Moreover, ZNF224 expression was significantly lowered after conventional chemotherapy treatment in a subset of CLL patients. By in vitro experiments we confirmed that ZNF224 expression is suppressed by fludarabine and demonstrated that ZNF224 is involved in apoptosis resistance in CLL cells. Moreover, we showed that ZNF224 positively modulates cyclin D3 gene expression. Consistently, we observed that alteration of ZNF224 expression leads to defects in cell cycle control. All together, our results strongly suggest that in CLL cells high expression level of ZNF224 can lead to inappropriate cell growth and apoptosis resistance, thus contributing to CLL progression. Targeting ZNF224 could thus improve CLL response to therapy.
慢性淋巴细胞白血病(CLL)与凋亡抵抗及细胞生长控制缺陷有关。我们的研究首次描述了KRAB锌指蛋白ZNF224在CLL中的关键作用。与对照细胞相比,在CLL患者中检测到高ZNF224转录水平。此外,在一部分CLL患者中,传统化疗治疗后ZNF224表达显著降低。通过体外实验,我们证实氟达拉滨可抑制ZNF224表达,并证明ZNF224参与CLL细胞的凋亡抵抗。此外,我们表明ZNF224正向调节细胞周期蛋白D3基因表达。一致地,我们观察到ZNF224表达的改变导致细胞周期控制缺陷。总之,我们的结果强烈表明,在CLL细胞中ZNF224的高表达水平可导致不适当的细胞生长和凋亡抵抗,从而促进CLL进展。因此,靶向ZNF224可改善CLL对治疗的反应。