Li Z, Abraham B J, Berezovskaya A, Farah N, Liu Y, Leon T, Fielding A, Tan S H, Sanda T, Weintraub A S, Li B, Shen S, Zhang J, Mansour M R, Young R A, Look A T
Department of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
Whitehead Institute for Biomedical Research, Cambridge, MA, USA.
Leukemia. 2017 Oct;31(10):2057-2064. doi: 10.1038/leu.2017.75. Epub 2017 Mar 6.
Oncogenic driver mutations are those that provide a proliferative or survival advantage to neoplastic cells, resulting in clonal selection. Although most cancer-causing mutations have been detected in the protein-coding regions of the cancer genome; driver mutations have recently also been discovered within noncoding genomic sequences. Thus, a current challenge is to gain precise understanding of how these unique genomic elements function in cancer pathogenesis, while clarifying mechanisms of gene regulation and identifying new targets for therapeutic intervention. Here we report a C-to-T single nucleotide transition that occurs as a somatic mutation in noncoding sequences 4 kb upstream of the transcriptional start site of the LMO1 oncogene in primary samples from patients with T-cell acute lymphoblastic leukaemia. This single nucleotide alteration conforms to an APOBEC-like cytidine deaminase mutational signature, and generates a new binding site for the MYB transcription factor, leading to the formation of an aberrant transcriptional enhancer complex that drives high levels of expression of the LMO1 oncogene. Since APOBEC-signature mutations are common in a broad spectrum of human cancers, we suggest that noncoding nucleotide transitions such as the one described here may activate potent oncogenic enhancers not only in T-lymphoid cells but in other cell lineages as well.
致癌驱动突变是指那些赋予肿瘤细胞增殖或生存优势从而导致克隆选择的突变。尽管大多数致癌突变已在癌症基因组的蛋白质编码区域中被检测到,但驱动突变最近也在非编码基因组序列中被发现。因此,当前的一个挑战是要精确了解这些独特的基因组元件在癌症发病机制中如何发挥作用,同时阐明基因调控机制并确定治疗干预的新靶点。在此,我们报告了在T细胞急性淋巴细胞白血病患者的原发性样本中,LMO1致癌基因转录起始位点上游4 kb的非编码序列中发生的一个C到T的单核苷酸转变,该转变为体细胞突变。这种单核苷酸改变符合APOBEC样胞苷脱氨酶突变特征,并为MYB转录因子产生了一个新的结合位点,导致形成异常转录增强子复合物,驱动LMO1致癌基因的高水平表达。由于APOBEC特征性突变在广泛的人类癌症中很常见,我们认为这里描述的这种非编码核苷酸转变可能不仅在T淋巴细胞中,而且在其他细胞谱系中激活强大的致癌增强子。