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MTAP-CDKN2A 基因座赋予犬自然发生癌症的易感性。

The MTAP-CDKN2A locus confers susceptibility to a naturally occurring canine cancer.

机构信息

Cancer Genetics Branch, National Human Genome Research Institute, NIH, Bethesda, MD 20892, USA.

出版信息

Cancer Epidemiol Biomarkers Prev. 2012 Jul;21(7):1019-27. doi: 10.1158/1055-9965.EPI-12-0190-T. Epub 2012 May 23.

Abstract

BACKGROUND

Advantages offered by canine population substructure, combined with clinical presentations similar to human disorders, makes the dog an attractive system for studies of cancer genetics. Cancers that have been difficult to study in human families or populations are of particular interest. Histiocytic sarcoma is a rare and poorly understood neoplasm in humans that occurs in 15% to 25% of Bernese Mountain Dogs (BMD).

METHODS

Genomic DNA was collected from affected and unaffected BMD in North America and Europe. Both independent and combined genome-wide association studies (GWAS) were used to identify cancer-associated loci. Fine mapping and sequencing narrowed the primary locus to a single gene region.

RESULTS

Both populations shared the same primary locus, which features a single haplotype spanning MTAP and part of CDKN2A and is present in 96% of affected BMD. The haplotype is within the region homologous to human chromosome 9p21, which has been implicated in several types of cancer.

CONCLUSIONS

We present the first GWAS for histiocytic sarcoma in any species. The data identify an associated haplotype in the highly cited tumor suppressor locus near CDKN2A. These data show the power of studying distinctive malignancies in highly predisposed dog breeds.

IMPACT

Here, we establish a naturally occurring model of cancer susceptibility due to CDKN2 dysregulation, thus providing insight about this cancer-associated, complex, and poorly understood genomic region.

摘要

背景

犬种群亚结构所提供的优势,加上与人类疾病相似的临床表现,使得犬成为癌症遗传学研究的一个有吸引力的系统。特别感兴趣的是那些在人类家庭或人群中难以研究的癌症。组织细胞肉瘤是一种在人类中罕见且尚未被充分了解的肿瘤,在伯尔尼山犬(BMD)中约占 15%至 25%。

方法

从北美和欧洲受影响和未受影响的 BMD 中收集基因组 DNA。使用独立和联合全基因组关联研究(GWAS)来识别与癌症相关的基因座。精细映射和测序将主要基因座缩小到单个基因区域。

结果

两个群体共享相同的主要基因座,该基因座具有跨越 MTAP 和部分 CDKN2A 的单一单倍型,存在于 96%的受影响的 BMD 中。该单倍型位于与人类 9p21 染色体同源的区域内,该区域与多种类型的癌症有关。

结论

我们首次在任何物种中进行了组织细胞肉瘤的全基因组关联研究。数据确定了与 CDKN2A 附近高度引用的肿瘤抑制基因座相关的单倍型。这些数据显示了在高度易感犬种中研究独特恶性肿瘤的力量。

影响

在这里,我们建立了一个由于 CDKN2 失调导致的癌症易感性的自然发生模型,从而提供了有关该与癌症相关的复杂且尚未被充分了解的基因组区域的见解。

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