[摘要]B025:肿瘤微环境中mRNA和蛋白的多重三维定位

S. S. Lee, D. Scholten, V. Bindokas, S. Kron
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摘要

检测肿瘤组织中致癌蛋白编码信使RNA (mRNA)是准确诊断肿瘤的关键检测方法。与癌症蛋白生物标志物分析一起,mRNA鉴定对于为个体患者匹配适当的治疗至关重要。同样,在治疗活检中,细胞因子mRNA定位可以通过识别淋巴细胞的类型和功能状态来评估免疫治疗的抗肿瘤反应,例如区分活化的细胞毒性t细胞和初始t细胞。为了评估mRNA的定位,活检通常是福尔马林固定和石蜡包埋(FFPE),切片切片,然后通过显色原位杂交(CISH)对mRNA进行染色。通过mRNA CISH分析样品通常需要几天时间,并且需要相当多的技术专长。多路荧光原位杂交技术(FISH)的最新进展使得在单个组织切片中同时分析多种mRNA类型成为可能。然而,即使完全表征,单个组织切片也不能充分代表肿瘤微环境的复杂三维(3D)结构。目前仍然迫切需要一种快速的样本到答案技术,用于亚细胞分辨率的mRNA多重3D成像,能够充分表征完整活检组织中的肿瘤微环境,用于癌症诊断和免疫治疗反应分析。为了解决这些挑战,我们采用了透明组织断层扫描(T3),一种简单快速的组织清除和多重3D成像方法,来分析肿瘤微环境中的mRNA分布。有了T3,致癌和免疫调节细胞因子mrna很容易在小鼠、患者来源的异种移植(PDX)和头颈部肿瘤的细胞类型和其他特征背景下定位。这项工作建立了T3作为肿瘤微环境中mRNA和蛋白质分布的定量、3D空间分析工具。引文格式:Steve Seung-Young Lee, David Scholten, Vytautas P. Bindokas, Stephen Kron。肿瘤微环境中mRNA和蛋白的多重三维定位[摘要]。第四届CRI-CIMT-EATI-AACR国际癌症免疫治疗会议:将科学转化为生存;2018年9月30日至10月3日;纽约,纽约。费城(PA): AACR;癌症免疫学杂志,2019;7(2增刊):摘要nr B025。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abstract B025: Multiplex three-dimensional mapping of mRNA and protein in the tumor microenvironment
Detecting oncogenic protein-coding messenger RNA (mRNA) in tumor tissues is a key assay for accurate cancer diagnosis. Along with cancer protein biomarker analysis, mRNA identification is critical for matching the appropriate treatment to individual patients. Likewise, cytokine mRNA localization in on-treatment biopsies enables evaluation of the antitumor response to immunotherapy by identifying the types and functional states of lymphocytes, for example distinguishing activated cytotoxic T-cells from naive T-cells. To assess mRNA localization, a biopsy is typically formalin fixed and paraffin embedded (FFPE), thin sections are cut, and then are stained for mRNA by chromogenic In situ hybridization (CISH). Analyzing samples by mRNA CISH typically takes a few days and requires considerable technical expertise. Recent progress in multiplexed fluorescence In situ hybridization (FISH) has enabled simultaneous analysis of multiple mRNA types in a single tissue section. Nonetheless, even if fully characterized, individual tissue sections cannot adequately represent the complex three-dimensional (3D) architecture of the tumor microenvironment. There remains a pressing need for a rapid sample-to-answer technology for multiplex 3D imaging of mRNA at sub-cellular resolution that is able to fully characterize the tumor microenvironment in intact biopsy tissues for cancer diagnosis and immunotherapeutic response analysis. To address these challenges, we have adapted Transparent Tissue Tomography (T3), a simple and fast tissue clearing and multiplex 3D imaging method, to analyze mRNA distribution in the tumor microenvironment. With T3, oncogenic and immunoregulatory cytokine mRNAs are readily localized in the context of cell types and other features in murine, patient derived xenograft (PDX), and head and neck tumors. This work establishes T3 as a tool for a quantitative, 3D spatial analysis of mRNA and protein distribution in the tumor microenvironment. Citation Format: Steve Seung-Young Lee, David Scholten, Vytautas P. Bindokas, Stephen Kron. Multiplex three-dimensional mapping of mRNA and protein in the tumor microenvironment [abstract]. In: Proceedings of the Fourth CRI-CIMT-EATI-AACR International Cancer Immunotherapy Conference: Translating Science into Survival; Sept 30-Oct 3, 2018; New York, NY. Philadelphia (PA): AACR; Cancer Immunol Res 2019;7(2 Suppl):Abstract nr B025.
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