Davis B, Schwartz M, Duchemin D, Carl Barrett J, Post G
Innogenics Inc, Harvard, MA.
HTG Molecular Inc, Tucson, AZ.
J Vet Intern Med. 2017 May;31(3):854-863. doi: 10.1111/jvim.14686. Epub 2017 Mar 29.
Use of molecular-based diagnostics for companion animals is impeded by availability of technology platforms, tissue acquisition requirements, and species-specific reagents.
HYPOTHESIS/OBJECTIVES: To validate a quantitative nuclease protection assay (qNPA) to simultaneously measure RNA expression of multiple genes in archived formalin-fixed paraffin-embedded (FFPE) tumors from dogs.
All tumor biopsy samples were collected retrospectively from surgical biopsies and in the care of veterinarians.
Retrospective case series. A qNPA 96-well ArrayPlate was built using 30 canine-specific genes, 5 housekeeping genes, positive and negative controls with qualified gene-specific oligonucleotides. Pearson's correlation, coefficient of variation (CV), and multivariate analysis were used to determine analytical performance using 40 FFPE dog tumors. Once validated, 70 FFPE dog tumors were analyzed for differences in gene expression using hierarchical clustering and analysis of variance of log transformed data. Immunohistochemistry (IHC) was performed to correlate gene expression and protein expression in a subset of tumors.
The assay was linear with decreasing sample input (R = 0.978), reproducible within and between 96-well plates (r = 0.988 and 0.95, respectively) and between different laboratories (CV = 0.96). Hierarchical cluster analysis showed grouping of tumors by histogenesis and oncogenes. Significant differences were found between BCl2, E2F transcription factor 1, MDM2, COX-2, MET proto-oncogene receptor kinase, and other biologically relevant gene expression in tumor subtypes. Immunohistochemistry confirmed protein expression.
Because this technology works reliably on FFPE specimens, it can help expedite the broad introduction of multiplexed genomic information for improved diagnostics and discovery of new targets for therapies in veterinary oncology.
技术平台的可用性、组织获取要求以及物种特异性试剂阻碍了分子诊断技术在伴侣动物中的应用。
假设/目标:验证一种定量核酸酶保护分析方法(qNPA),以同时测量犬类福尔马林固定石蜡包埋(FFPE)肿瘤中多个基因的RNA表达。
所有肿瘤活检样本均从手术活检中回顾性收集,并由兽医进行护理。
回顾性病例系列研究。使用30个犬类特异性基因、5个管家基因、阳性和阴性对照以及合格的基因特异性寡核苷酸构建qNPA 96孔阵列板。使用40个FFPE犬肿瘤样本,通过Pearson相关性分析、变异系数(CV)和多变量分析来确定分析性能。验证后,使用层次聚类和对数转换数据的方差分析对70个FFPE犬肿瘤样本的基因表达差异进行分析。对一部分肿瘤样本进行免疫组织化学(IHC)检测,以关联基因表达和蛋白质表达。
该分析方法在样本输入量减少时呈线性关系(R = 0.978),在96孔板内和板间具有可重复性(分别为r = 0.988和0.95),在不同实验室之间也具有可重复性(CV = 0.96)。层次聚类分析显示肿瘤按组织发生和癌基因进行分组。在肿瘤亚型中,BCl2、E2F转录因子1、MDM2、COX - 2、MET原癌基因受体激酶和其他生物学相关基因的表达存在显著差异。免疫组织化学证实了蛋白质表达。
由于该技术在FFPE样本上可靠运行,它有助于加快多重基因组信息的广泛应用,以改善兽医肿瘤学的诊断并发现新的治疗靶点。