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高通量 NanoString 分析人乳头瘤病毒致癌性与头颈部鳞状细胞癌肿瘤微环境转录组。

High-Throughput NanoString Analysis of Oncogenic Human Papillomavirus and Tumor Microenvironment Transcription in Head and Neck Squamous Cell Carcinoma.

机构信息

Department of Otolaryngology/Head and Neck Surgery, The University of North Carolina at Chapel Hill School of Medicine, Chapel Hill, North Carolina.

出版信息

Curr Protoc. 2021 May;1(5):e146. doi: 10.1002/cpz1.146.

Abstract

Human papillomaviruses (HPVs), specifically high-risk HPVs, are responsible for up to 3% of all cancers in women and up to 2% of all cancers in men. They have been identified as the etiological agent of cervical cancer and have been increasingly found to be the driver behind head and neck cancers of the oropharynx. A system in which we can simultaneously observe transcriptional changes to both a host's tumor microenvironment and its associated oncogenic driver (e.g., HPV) would be highly valuable for understanding HPV's role in tumorigenesis. This article describes a detailed methodology for utilizing high-throughput RNA analysis to study viral transcription in formalin-fixed, paraffin-embedded clinical tumor samples. Although our lab utilizes these methods for the study of head and neck cancer, the principles contained within are widely applicable to all fields of HPV study. © 2021 Wiley Periodicals LLC. Basic Protocol: HPV16 transcript analysis using NanoString Support Protocol 1: Preparation of RNA from formalin-fixed, paraffin-embedded slides Support Protocol 2: Preparation of RNA from cell lysates Support Protocol 3: Fluorometric RNA concentration and RNA integrity analysis Support Protocol 4: Determination of input RNA based on DV calculation.

摘要

人乳头瘤病毒(HPV),特别是高危 HPV,在女性中导致高达 3%的所有癌症,在男性中导致高达 2%的所有癌症。它们已被确定为宫颈癌的病因,并越来越多地被发现是口咽头颈部癌症的驱动因素。如果有一种系统能够同时观察宿主肿瘤微环境及其相关致癌驱动因素(例如 HPV)的转录变化,这对于理解 HPV 在肿瘤发生中的作用将非常有价值。本文描述了一种利用高通量 RNA 分析研究福尔马林固定、石蜡包埋临床肿瘤样本中病毒转录的详细方法。尽管我们的实验室利用这些方法研究头颈部癌症,但其中包含的原理广泛适用于 HPV 研究的所有领域。© 2021 Wiley Periodicals LLC. 基本方案:使用 NanoString 分析 HPV16 转录 支持方案 1:从福尔马林固定、石蜡包埋的载玻片上制备 RNA 支持方案 2:从细胞裂解物中制备 RNA 支持方案 3:荧光 RNA 浓度和 RNA 完整性分析 支持方案 4:根据 DV 计算确定输入 RNA。

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