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镶嵌型20号染色体长臂缺失在老年人群中更为常见。

Mosaic chromosome 20q deletions are more frequent in the aging population.

作者信息

Machiela Mitchell J, Zhou Weiyin, Caporaso Neil, Dean Michael, Gapstur Susan M, Goldin Lynn, Rothman Nathaniel, Stevens Victoria L, Yeager Meredith, Chanock Stephen J

机构信息

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, MD.

Cancer Genomics Research Laboratory, Leidos Biomedical Research Inc., Frederick, MD; and.

出版信息

Blood Adv. 2017 Feb 13;1(6):380-385. doi: 10.1182/bloodadvances.2016003129. eCollection 2017 Feb 14.

DOI:10.1182/bloodadvances.2016003129
PMID:29296952
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5738991/
Abstract

Deletions on the long-arm of chromosome 20, del(20q), are common karyotypic abnormalities in myeloid disorders. Bioinformatic analyses of the B-allele frequency and log R ratio values from genome-wide association data have identified individuals who are mosaic for large structural abnormalities (>2 Mb). We investigated the most common autosomal event, namely mosaic del(20q), in 46 254 nonhematologic cancer cases and 36 229 cancer-free controls. We detected 91 mosaic del(20q) in leukocytes (80%) and buccal material (20%). The mosaic del(20q) mapped to a well-characterized minimally deleted region (MDR) reported in myeloid disorders. Common breakpoint clusters map to the coordinates of 29.9 to 31.5 Mb on the centromeric side of mosaic del(20q), and 42.0 to 45.4 Mb and 48.1 to 50.7 Mb on the telomeric end (GRCh36). Multivariate analyses suggest del(20q) increases with age, and is more common in males but less common in individuals of African ancestry. No conclusive associations were noted between the presence of mosaic del(20q) and subsequent solid tumor risk. Our observations demonstrate that the MDR of del(20q) is the most common large scale mosaic autosomal abnormality in whole blood and has a frequency of ∼1 in every 1000 adults over the age of 50, which exceeds the expected incidence of myeloid leukemia in the population. Our results indicate that subclonal mosaic events of a region implicated in myeloid disorders on 20q are more frequent than the predicted population-estimated incidence of myeloid diseases, and thus suggest that these events can be tolerated until additional events accumulate that drive myeloid disorders.

摘要

20号染色体长臂缺失(del(20q))是髓系疾病中常见的核型异常。通过对全基因组关联数据中的B等位基因频率和对数R比值进行生物信息学分析,已识别出存在大于2 Mb大结构异常的嵌合体个体。我们在46254例非血液系统癌症病例和36229例无癌对照中研究了最常见的常染色体事件,即嵌合性del(20q)。我们在白细胞(80%)和颊黏膜组织(20%)中检测到91例嵌合性del(20q)。嵌合性del(20q)定位于髓系疾病中报道的一个特征明确的最小缺失区域(MDR)。常见的断点簇定位于嵌合性del(20q)着丝粒侧29.9至31.5 Mb处,以及端粒末端42.0至45.4 Mb和48.1至50.7 Mb处(GRCh36)。多变量分析表明,del(20q)随年龄增加,在男性中更常见,但在非洲裔个体中较少见。嵌合性del(20q)的存在与随后的实体瘤风险之间未发现确凿关联。我们的观察结果表明,del(20q)的MDR是全血中最常见的大规模嵌合常染色体异常,在50岁以上的成年人中,其频率约为每1000人中有1例,超过了人群中髓系白血病的预期发病率。我们的结果表明,20q上与髓系疾病相关区域中的亚克隆嵌合事件比预测的人群估计髓系疾病发病率更频繁,因此表明这些事件在驱动髓系疾病的其他事件积累之前可以被耐受。

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