Pekarsky Yuri, Santanam Urmila, Cimmino Amelia, Palamarchuk Alexey, Efanov Alexey, Maximov Vadim, Volinia Stefano, Alder Hansjuerg, Liu Chang-Gong, Rassenti Laura, Calin George A, Hagan John P, Kipps Thomas, Croce Carlo M
Comprehensive Cancer Center, Human Cancer Genetics Program and Department of Molecular Virology, Immunology, and Medical Genetics, OSU School of Medicine, Ohio State University, Columbus, Ohio 43210, USA.
Cancer Res. 2006 Dec 15;66(24):11590-3. doi: 10.1158/0008-5472.CAN-06-3613.
B-cell chronic lymphocytic leukemia (B-CLL) is the most common human leukemia in the world. Deregulation of the TCL1 oncogene is a causal event in the pathogenesis of the aggressive form of this disease as was verified by using animal models. To study the mechanism of Tcl1 regulation in CLL, we carried out microRNA expression profiling of three types of CLL: indolent CLL, aggressive CLL, and aggressive CLL showing 11q deletion. We identified distinct microRNA signatures corresponding to each group of CLL. We further determined that Tcl1 expression is regulated by miR-29 and miR-181, two microRNAs differentially expressed in CLL. Expression levels of miR-29 and miR-181 generally inversely correlated with Tcl1 expression in the CLL samples we examined. Our results suggest that Tcl1 expression in CLL is, at least in part, regulated by miR-29 and miR-181 and that these microRNAs may be candidates for therapeutic agents in CLLs overexpressing Tcl1.
B细胞慢性淋巴细胞白血病(B-CLL)是世界上最常见的人类白血病。TCL1癌基因的失调是这种疾病侵袭性形式发病机制中的一个因果事件,这已通过动物模型得到验证。为了研究CLL中Tcl1调控的机制,我们对三种类型的CLL进行了微小RNA表达谱分析:惰性CLL、侵袭性CLL和显示11q缺失的侵袭性CLL。我们鉴定出了与每组CLL相对应的独特微小RNA特征。我们进一步确定Tcl1表达受miR-29和miR-181调控,这两种微小RNA在CLL中差异表达。在我们检测的CLL样本中,miR-29和miR-181的表达水平通常与Tcl1表达呈负相关。我们的结果表明,CLL中Tcl1的表达至少部分受miR-29和miR-181调控,并且这些微小RNA可能是过表达Tcl1的CLL治疗药物的候选者。