Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX 77030, USA.
Urologic Oncology Branch, Center for Cancer Research, National Cancer Institute, CRC Room 1W-5940, Bethesda, MD 20892, USA.
Cancer Cell. 2014 Sep 8;26(3):319-330. doi: 10.1016/j.ccr.2014.07.014. Epub 2014 Aug 21.
We describe the landscape of somatic genomic alterations of 66 chromophobe renal cell carcinomas (ChRCCs) on the basis of multidimensional and comprehensive characterization, including mtDNA and whole-genome sequencing. The result is consistent that ChRCC originates from the distal nephron compared with other kidney cancers with more proximal origins. Combined mtDNA and gene expression analysis implicates changes in mitochondrial function as a component of the disease biology, while suggesting alternative roles for mtDNA mutations in cancers relying on oxidative phosphorylation. Genomic rearrangements lead to recurrent structural breakpoints within TERT promoter region, which correlates with highly elevated TERT expression and manifestation of kataegis, representing a mechanism of TERT upregulation in cancer distinct from previously observed amplifications and point mutations.
我们基于多维和全面的特征描述了 66 例嫌色细胞肾细胞癌(ChRCC)的体细胞基因组改变景观,包括 mtDNA 和全基因组测序。结果与其他起源于近端肾单位的肾癌不同,ChRCC 起源于远端肾单位。联合 mtDNA 和基因表达分析表明,线粒体功能的改变是疾病生物学的一个组成部分,同时提示 mtDNA 突变在依赖氧化磷酸化的癌症中的作用不同。基因组重排导致 TERT 启动子区域内的重复结构断点,与高度升高的 TERT 表达和 kataegis 的表现相关,这代表了一种不同于先前观察到的扩增和点突变的癌症中 TERT 上调的机制。