Neupane Manish, Clark Allison P, Landini Serena, Birkbak Nicolai J, Eklund Aron C, Lim Elgene, Culhane Aedin C, Barry William T, Schumacher Steven E, Beroukhim Rameen, Szallasi Zoltan, Vidal Marc, Hill David E, Silver Daniel P
Department of Cancer Biology, Dana-Farber Cancer Institute, Boston, Massachusetts. Department of Medicine, Harvard Medical School, Boston, Massachusetts.
Department of Cancer Biology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Cancer Discov. 2016 Jan;6(1):45-58. doi: 10.1158/2159-8290.CD-15-0341. Epub 2015 Nov 6.
An unbiased genome-scale screen for unmutated genes that drive cancer growth when overexpressed identified methyl cytosine-guanine dinucleotide (CpG) binding protein 2 (MECP2) as a novel oncogene. MECP2 resides in a region of the X-chromosome that is significantly amplified across 18% of cancers, and many cancer cell lines have amplified, overexpressed MECP2 and are dependent on MECP2 expression for growth. MECP2 copy-number gain and RAS family member alterations are mutually exclusive in several cancer types. The MECP2 splicing isoforms activate the major growth factor pathways targeted by activated RAS, the MAPK and PI3K pathways. MECP2 rescued the growth of a KRAS(G12C)-addicted cell line after KRAS downregulation, and activated KRAS rescues the growth of an MECP2-addicted cell line after MECP2 downregulation. MECP2 binding to the epigenetic modification 5-hydroxymethylcytosine is required for efficient transformation. These observations suggest that MECP2 is a commonly amplified oncogene with an unusual epigenetic mode of action.
MECP2 is a commonly amplified oncogene in human malignancies with a unique epigenetic mechanism of action. Cancer Discov; 6(1); 45-58. ©2015 AACR.This article is highlighted in the In This Issue feature, p. 1.
一项无偏差的全基因组筛选,旨在寻找过表达时能驱动癌症生长的未突变基因,结果确定甲基胞嘧啶 - 鸟嘌呤二核苷酸(CpG)结合蛋白2(MECP2)为一种新型癌基因。MECP2位于X染色体的一个区域,在18%的癌症中该区域显著扩增,许多癌细胞系都有MECP2的扩增、过表达,且其生长依赖于MECP2的表达。在几种癌症类型中,MECP2拷贝数增加和RAS家族成员改变是相互排斥的。MECP2的剪接异构体激活了由活化RAS靶向的主要生长因子途径,即MAPK和PI3K途径。在KRAS下调后,MECP2挽救了KRAS(G12C)成瘾细胞系的生长,而活化的KRAS在MECP2下调后挽救了MECP2成瘾细胞系的生长。MECP2与表观遗传修饰5 - 羟甲基胞嘧啶的结合是有效转化所必需的。这些观察结果表明,MECP2是一种常见的扩增癌基因,具有不同寻常的表观遗传作用模式。
MECP2是人类恶性肿瘤中常见的扩增癌基因,具有独特的表观遗传作用机制。《癌症发现》;6(1);45 - 58。©2015美国癌症研究协会。本文在本期特刊第1页重点介绍。