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利用 HTG EdgeSeq 平台,从小且经苏木精和伊红染色的临床福尔马林固定、石蜡包埋标本中获得可靠的基因表达谱分析。

Reliable Gene Expression Profiling from Small and Hematoxylin and Eosin-Stained Clinical Formalin-Fixed, Paraffin-Embedded Specimens Using the HTG EdgeSeq Platform.

机构信息

Translational Medicine, Bristol-Myers Squibb, Princeton, New Jersey.

Translational Medicine, Bristol-Myers Squibb, Princeton, New Jersey.

出版信息

J Mol Diagn. 2019 Sep;21(5):796-807. doi: 10.1016/j.jmoldx.2019.04.011. Epub 2019 Jun 27.

Abstract

Clinical biomarker studies are often hindered by the scarcity or suboptimal quality of biological specimens. EdgeSeq, a transcriptomics analysis platform, combines quantitative nuclease protection assay technology with next-generation sequencing, using small amounts of starting material and delivering reproducible gene expression profiles from challenging material, such as formalin-fixed, paraffin-embedded (FFPE) tissue. To evaluate EdgeSeq for analysis of archives of stained FFPE tissue, EdgeSeq was performed on unstained, hematoxylin and eosin (H&E)-stained, and immunohistochemistry-stained slides from patients with small-cell and non-small-cell lung cancer. Pairwise comparisons of gene expression profiles from stained and unstained slides showed higher Pearson correlation coefficients with H&E staining (0.86 to 0.97) than with immunohistochemistry staining (0.21 to 0.56). A 25-gene interferon-γ signature score from unstained slides showed a Pearson correlation coefficient of 0.92 with H&E-stained slides and a significant Spearman correlation (P = 0.0025) with immune scores. To test gene expression profiling in small samples, FFPE sample equivalents were examined from 5.0 to 0.08 mm of a section (5 μm thick); sample equivalents ≥0.31 mm showed alignment rates >69% and pairwise Pearson correlation coefficients ≥0.87. EdgeSeq can, thus, be used to profile small and H&E-stained FFPE tumor specimens to obtain biomarker data from limited tissue in oncology clinical trials and enable research into tumor microenvironment and immune cell engagement with tumors at the locoregional level.

摘要

临床生物标志物研究通常受到生物标本稀缺或质量欠佳的限制。EdgeSeq 是一种转录组分析平台,它结合了定量核酸酶保护分析技术和下一代测序技术,使用少量起始材料,从福尔马林固定石蜡包埋(FFPE)组织等具有挑战性的材料中提供可重复的基因表达谱。为了评估 EdgeSeq 对染色 FFPE 组织存档的分析,对小细胞肺癌和非小细胞肺癌患者的未染色、苏木精和伊红(H&E)染色和免疫组织化学染色的载玻片进行了 EdgeSeq 分析。染色和未染色载玻片的基因表达谱的两两比较显示,与免疫组织化学染色(0.21 至 0.56)相比,与 H&E 染色(0.86 至 0.97)的 Pearson 相关系数更高。来自未染色载玻片的 25 个基因干扰素-γ特征评分与 H&E 染色载玻片的 Pearson 相关系数为 0.92,与免疫评分具有显著的 Spearman 相关性(P = 0.0025)。为了在小样本中测试基因表达谱,从 5.0 至 0.08 mm 厚的切片(5μm 厚)中检查 FFPE 样本等效物;样本当量≥0.31mm 时,对齐率>69%,两两 Pearson 相关系数≥0.87。因此,EdgeSeq 可用于分析小的和 H&E 染色的 FFPE 肿瘤标本,以从肿瘤临床试验中的有限组织中获得生物标志物数据,并能够研究肿瘤微环境和免疫细胞与肿瘤的局部区域水平的相互作用。

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