Department of Cancer Biology and Genetics, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Curr Top Microbiol Immunol. 2017;407:191-203. doi: 10.1007/82_2017_34.
This paper describes how we discovered the juxtaposition of the MYC gene to the human immunoglobulin loci and how that finding was extended to characterize molecularly the t(14;18) chromosome translocation of follicular lymphoma and to clone the BCL2 gene. BCL2 is also overexpressed in CLL, the most common human leukemia. We discovered that most of human CLLs have a deletion of two microRNAs residing in the same polycistronic RNA, miR-15a and miR-16-1, and that these two microRNAs are negative regulators of BCL2. Thus, loss of miR-15/16 leads to overexpression of BCL2 that can be targeted by the new drug, venetoclax, that was recently approved by the FDA for the treatment of aggressive CLLs.
本文描述了我们如何发现 MYC 基因与人类免疫球蛋白基因座的并置,以及如何扩展这一发现来对滤泡性淋巴瘤的 t(14;18)染色体易位进行分子特征分析,并克隆 BCL2 基因。BCL2 在慢性淋巴细胞白血病(CLL)中也过表达,CLL 是最常见的人类白血病。我们发现,大多数人类 CLL 都存在两个微 RNA(miR-15a 和 miR-16-1)所在的多顺反子 RNA 的缺失,这两个 microRNA 是 BCL2 的负调控因子。因此,miR-15/16 的缺失导致 BCL2 的过表达,而新型药物 venetoclax 可以靶向 BCL2,最近被 FDA 批准用于治疗侵袭性 CLL。