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用于犬类福尔马林固定石蜡包埋乳腺肿瘤中 及 变异检测的AmpliSeq二代测序 panel 的验证

Validation of AmpliSeq NGS Panel for and Variant Detection in Canine Formalin-Fixed Paraffin-Embedded Mammary Tumors.

作者信息

Di Giacomo Daniela, Di Domenico Marco, Defourny Sabrina Vanessa Patrizia, Malatesta Daniela, Di Teodoro Giovanni, Martino Michele, Viola Antonello, D'Alterio Nicola, Cammà Cesare, Modesto Paola, Petrini Antonio

机构信息

Istituto Zooprofilattico Sperimentale dell'Abruzzo e del Molise "G. Caporale", Campo Boario, 64100 Teramo, Italy.

National Reference Center for Whole Genome Sequencing of Microbial Pathogens: Database and Bioinformatic Analysis, Istituto Zooprofilattico Sperimentale dell'Abruzzo e del Molise, Campo Boario, 64100 Teramo, Italy.

出版信息

Life (Basel). 2022 Jun 7;12(6):851. doi: 10.3390/life12060851.

Abstract

Mammary carcinomas are the most common neoplasms observed in women and in female dogs. Canine mammary tumors show epidemiological, clinical, genetic, and prognostic characteristics comparable to human breast cancers. The recent introduction of next generation sequencing (NGS) technologies has greatly improved research and diagnostics for humans, while these new tools still need to be implemented in animal models. In this study we developed and validated an AmpliSeq Panel assay for the identification of BRCA variants in twenty-two different dogs. The amplicon mean coverage was 5499× and uniformity was higher than 98% in all samples. The results of germline single nucleotide variants (SNVs) and insertions/deletions (INDELs) were fully concordant regardless of the types of samples considered (blood, fresh and FFPE tissues). Moreover, despite the high DNA degradation observed in older FFPE blocks (>5 years), the assay allowed full coverage of all amplicons for downstream analyses. We consider the NGS panel developed in this study as a useful tool for expanding information on BRCA genes in the veterinary field and for human health from a comparative oncology perspective.

摘要

乳腺癌是女性和雌性犬类中最常见的肿瘤。犬乳腺肿瘤在流行病学、临床、遗传和预后特征方面与人类乳腺癌相似。新一代测序(NGS)技术的引入极大地改善了人类的研究和诊断,而这些新工具仍需在动物模型中应用。在本研究中,我们开发并验证了一种用于鉴定22只不同犬类中BRCA变异的AmpliSeq Panel检测方法。所有样本的扩增子平均覆盖度为5499倍,一致性高于98%。无论所考虑的样本类型(血液、新鲜组织和福尔马林固定石蜡包埋组织)如何,种系单核苷酸变异(SNV)和插入/缺失(INDEL)的结果完全一致。此外,尽管在较旧的福尔马林固定石蜡包埋组织块(>5年)中观察到高度的DNA降解,但该检测方法仍能对所有扩增子进行完全覆盖以供下游分析。我们认为本研究中开发的NGS检测板是从比较肿瘤学角度扩展兽医领域BRCA基因信息以及对人类健康有益的有用工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26f6/9225004/e42128ce60c9/life-12-00851-g001.jpg

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