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Y 染色体缺失导致透明细胞肾细胞癌中 KDM5D 和 KDM6C 表观遗传修饰物的下调。

Loss of chromosome Y leads to down regulation of KDM5D and KDM6C epigenetic modifiers in clear cell renal cell carcinoma.

机构信息

Department of Human Genetics, McGill University, 1205 Dr Penfield Avenue, Montreal, QC, H3A 1B1, Canada.

McGill University and Genome Quebec Innovation Centre, 740 Doctor Penfield Avenue, Montreal, QC, H3A 0G1, Canada.

出版信息

Sci Rep. 2017 Mar 23;7:44876. doi: 10.1038/srep44876.

Abstract

Recent genomic studies of sporadic clear cell renal cell carcinoma (ccRCC) have uncovered novel driver genes and pathways. Given the unequal incidence rates among men and women (male:female incidence ratio approaches 2:1), we compared the genome-wide distribution of the chromosomal abnormalities in both sexes. We observed a higher frequency for the somatic recurrent chromosomal copy number variations (CNVs) of autosomes in male subjects, whereas somatic loss of chromosome X was detected exclusively in female patients (17.1%). Furthermore, somatic loss of chromosome Y (LOY) was detected in about 40% of male subjects, while mosaic LOY was detected in DNA isolated from peripheral blood in 9.6% of them, and was the only recurrent CNV in constitutional DNA samples. LOY in constitutional DNA, but not in tumor DNA was associated with older age. Amongst Y-linked genes that were downregulated due to LOY, KDM5D and KDM6C epigenetic modifiers have functionally-similar X-linked homologs whose deficiency is involved in ccRCC progression. Our findings establish somatic LOY as a highly recurrent genetic defect in ccRCC that leads to downregulation of hitherto unsuspected epigenetic factors, and suggest that different mechanisms may underlie the somatic and mosaic LOY observed in tumors and peripheral blood, respectively.

摘要

最近对散发性透明细胞肾细胞癌 (ccRCC) 的基因组研究揭示了新的驱动基因和途径。鉴于男性和女性之间发病率的不平等(男性:女性发病率比接近 2:1),我们比较了两性中体细胞染色体异常的全基因组分布。我们观察到男性患者体细胞常染色体重复染色体拷贝数变异 (CNV) 的频率更高,而仅在女性患者中检测到体细胞丢失的 X 染色体(17.1%)。此外,在大约 40%的男性患者中检测到体细胞丢失的 Y 染色体(LOY),在其中 9.6%的患者的外周血分离的 DNA 中检测到镶嵌性 LOY,并且是唯一在正常组织 DNA 样本中反复出现的 CNV。正常组织 DNA 中的 LOY 与肿瘤 DNA 无关,与年龄较大有关。由于 LOY 而下调的 Y 连锁基因中,KDM5D 和 KDM6C 表观遗传修饰因子具有功能相似的 X 连锁同源物,其缺失与 ccRCC 的进展有关。我们的发现确立了体细胞 LOY 是 ccRCC 中一种高度反复出现的遗传缺陷,导致迄今为止未被怀疑的表观遗传因素下调,并表明不同的机制可能分别导致肿瘤和外周血中观察到的体细胞和镶嵌性 LOY。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccde/5362952/1e77f88e7840/srep44876-f1.jpg

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