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DNA 修复缺陷作为金毛寻回猎犬自发性淋巴瘤的易感性标志物:一项病例对照研究。

DNA repair deficiency as a susceptibility marker for spontaneous lymphoma in golden retriever dogs: a case-control study.

机构信息

Flint Animal Cancer Center, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Fort Collins, Colorado, United States of America.

出版信息

PLoS One. 2013 Jul 23;8(7):e69192. doi: 10.1371/journal.pone.0069192. Print 2013.

Abstract

There is accumulating evidence that an individual's inability to accurately repair DNA damage in a timely fashion may in part dictate a predisposition to cancer. Dogs spontaneously develop lymphoproliferative diseases such as lymphoma, with the golden retriever (GR) breed being at especially high risk. Mechanisms underlying such breed susceptibility are largely unknown; however, studies of heritable cancer predisposition in dogs may be much more straightforward than similar studies in humans, owing to a high degree of inbreeding and more limited genetic heterogeneity. Here, we conducted a pilot study with 21 GR with lymphoma, 20 age-matched healthy GR and 20 age-matched healthy mixed-breed dogs (MBD) to evaluate DNA repair capability following exposure to either ionizing radiation (IR) or the chemical mutagen bleomycin. Inter-individual variation in DNA repair capacity was evaluated in stimulated canine lymphoctyes exposed in vitro utilizing the G2 chromosomal radiosensitivity assay to quantify clastogen-induced chromatid-type aberrations (gaps and breaks). Golden retrievers with lymphoma demonstrated elevated sensitivity to induction of chromosome damage following either challenge compared to either healthy GR or MBD at multiple doses and time points. Using the 75(th) percentile of chromatid breaks per 1,000 chromosomes in the MBD population at 4 hours post 1.0 Gy IR exposure as a benchmark to compare cases and controls, GR with lymphoma were more likely than healthy GR to be classified as "sensitive" (odds ratio = 21.2, 95% confidence interval 2.3-195.8). Furthermore, our preliminary findings imply individual (rather than breed) susceptibility, and suggest that deficiencies in heritable factors related to DNA repair capabilities may be involved in the development of canine lymphoma. These studies set the stage for larger confirmatory studies, as well as candidate-based approaches to probe specific genetic susceptibility factors.

摘要

越来越多的证据表明,个体不能及时准确地修复 DNA 损伤,这可能在一定程度上决定了癌症易感性。狗会自发地患上淋巴增生性疾病,如淋巴瘤,其中金毛猎犬(GR)品种的患病风险特别高。导致这种品种易感性的机制在很大程度上尚不清楚;然而,由于高度近亲繁殖和遗传异质性有限,研究狗的遗传性癌症易感性可能比在人类中进行类似的研究要简单得多。在这里,我们对 21 只患有淋巴瘤的 GR、20 只年龄匹配的健康 GR 和 20 只年龄匹配的健康杂种犬(MBD)进行了一项初步研究,以评估在暴露于电离辐射(IR)或化学诱变剂博莱霉素后 DNA 修复能力。通过体外刺激犬淋巴细胞利用 G2 染色体辐射敏感性测定法评估个体间的 DNA 修复能力,以量化致裂剂诱导的染色单体型畸变(裂隙和断裂)。与健康的 GR 或 MBD 相比,患有淋巴瘤的 GR 在多个剂量和时间点暴露于任何一种挑战后,染色体损伤的诱导敏感性均升高。以 MBD 群体中 4 小时 1.0 Gy IR 暴露后每 1000 条染色体中的 75%的染色单体断裂数作为基准来比较病例和对照组,患有淋巴瘤的 GR 比健康的 GR 更有可能被归类为“敏感”(比值比=21.2,95%置信区间 2.3-195.8)。此外,我们的初步发现表明个体(而不是品种)易感性,并表明与 DNA 修复能力相关的遗传性因素缺陷可能参与了犬淋巴瘤的发生。这些研究为更大规模的验证性研究以及基于候选基因的方法研究特定的遗传易感性因素奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d171/3720645/d045e42b3ad7/pone.0069192.g001.jpg

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