Floros Kostas V, Talieri Maroulio, Scorilas Andreas
Department of Biochemistry and Molecular Biology, Faculty of Biology, University of Athens, GR-15701, Athens, Greece.
Biol Chem. 2006 Dec;387(12):1629-33. doi: 10.1515/BC.2006.203.
The BCL2 family of genes (B-cell CLL/lymphoma 2; Bcl-2) plays a pivotal role in the highly regulated process of apoptosis. We have recently cloned a newly identified member of this family, BCL2L12, which was found to be differentially expressed in many tumors. It is known that topotecan and methotrexate act through induction of apoptosis in cancer cells. In the present study we investigated the expression profile of the novel apoptotic gene BCL2L12 in relation to other apoptotic genes in the human leukemic cell line HL-60, after treatment with topotecan or methotrexate. The kinetics of apoptosis induction and cell toxicity were investigated by DNA laddering and the MTT method, respectively. Gene expression levels were analyzed by RT-PCR using gene-specific primers. Downregulation of BCL2L12, BCL2 and FAS was observed after treatment of HL-60 cells with topotecan, while treatment with methotrexate led to downregulation of BCL2 and FAS, with no change in BCL2L12 expression. Our results support the significance of mRNA modulations in the expression of apoptosis-related genes during treatment of human leukemic cells with anticancer drugs.
BCL2基因家族(B细胞慢性淋巴细胞白血病/淋巴瘤2;Bcl-2)在高度调控的细胞凋亡过程中起关键作用。我们最近克隆了该家族一个新鉴定的成员BCL2L12,发现它在许多肿瘤中存在差异表达。已知拓扑替康和甲氨蝶呤通过诱导癌细胞凋亡发挥作用。在本研究中,我们在用拓扑替康或甲氨蝶呤处理人白血病细胞系HL-60后,研究了新型凋亡基因BCL2L12与其他凋亡基因相关的表达谱。分别通过DNA梯状条带分析和MTT法研究凋亡诱导动力学和细胞毒性。使用基因特异性引物通过RT-PCR分析基因表达水平。用拓扑替康处理HL-60细胞后,观察到BCL2L12、BCL2和FAS下调,而用甲氨蝶呤处理导致BCL2和FAS下调,BCL2L12表达无变化。我们的结果支持在用抗癌药物治疗人白血病细胞期间,mRNA调节在凋亡相关基因表达中的重要性。