一种高度敏感的组织特异性qrt - pcr检测肿瘤引流淋巴结黑色素瘤细胞的方法

Kristian M. Hargadon, Travis B. Goodloe III
{"title":"一种高度敏感的组织特异性qrt - pcr检测肿瘤引流淋巴结黑色素瘤细胞的方法","authors":"Kristian M. Hargadon,&nbsp;Travis B. Goodloe III","doi":"10.1002/cpz1.70139","DOIUrl":null,"url":null,"abstract":"<p>Melanoma invasion of regional lymph nodes, a critical event in the progression of this disease, is well documented as a poor prognostic factor for patients with melanoma. Assessing lymph node involvement is therefore a routine part of the diagnostic workup for patients presenting with melanoma at a T stage of ≥T2a. In clinical settings, the status and degree of melanoma lymph node involvement is traditionally characterized by histopathological analysis of tissue obtained during a sentinel lymph node biopsy, a labor-intensive and costly approach that requires technically challenging sample preparation and interpretation by a trained pathologist. Alternative approaches that might reduce the financial burden and turnaround time of a sentinel lymph node biopsy workup are therefore desirable. Likewise, the ability to accurately assess lymph node invasion by melanoma in experimental settings is necessary to gain new insights into mechanisms of distant metastasis and tumor-associated immune suppression. With these applications in mind, we recently developed, and describe herein, a tissue-specific qRT-PCR-based protocol for detecting melanoma cells within tumor-draining lymph nodes. Using murine models of lymph-node-invasive and lymph-node-noninvasive melanoma cell lines and a melanin-biosynthesis-pathway-specific <i>Trp2</i> gene expression assay, we validated this method as a highly sensitive strategy for assessing lymph node involvement by melanoma. © 2025 Wiley Periodicals LLC.</p><p><b>Basic Protocol 1</b>: Growth and maintenance of murine melanoma cell cultures</p><p><b>Basic Protocol 2</b>: Extraction and quantification of RNA from murine melanoma cultures</p><p><b>Basic Protocol 3</b>: cDNA synthesis via reverse transcription</p><p><b>Basic Protocol 4</b>: Probe and primer design for TaqMan-based qPCR</p><p><b>Basic Protocol 5</b>: qPCR analysis of tissue-specific <i>Trp2</i> gene expression</p><p><b>Basic Protocol 6</b>: <i>In vitro</i> validation of qRT-PCR <i>Trp2</i> gene expression assay for detection of melanoma cells in murine whole lymph node preparations</p><p><b>Basic Protocol 7</b>: <i>In vivo</i> validation of qRT-PCR <i>Trp2</i> gene expression assay for detection of melanoma cells in murine tumor-draining lymph nodes</p>","PeriodicalId":93970,"journal":{"name":"Current protocols","volume":"5 4","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-04-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A Highly Sensitive Tissue-specific qRT-PCR-based Assay for Detection of Melanoma Cells in Tumor-Draining Lymph Nodes\",\"authors\":\"Kristian M. Hargadon,&nbsp;Travis B. Goodloe III\",\"doi\":\"10.1002/cpz1.70139\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Melanoma invasion of regional lymph nodes, a critical event in the progression of this disease, is well documented as a poor prognostic factor for patients with melanoma. Assessing lymph node involvement is therefore a routine part of the diagnostic workup for patients presenting with melanoma at a T stage of ≥T2a. In clinical settings, the status and degree of melanoma lymph node involvement is traditionally characterized by histopathological analysis of tissue obtained during a sentinel lymph node biopsy, a labor-intensive and costly approach that requires technically challenging sample preparation and interpretation by a trained pathologist. Alternative approaches that might reduce the financial burden and turnaround time of a sentinel lymph node biopsy workup are therefore desirable. Likewise, the ability to accurately assess lymph node invasion by melanoma in experimental settings is necessary to gain new insights into mechanisms of distant metastasis and tumor-associated immune suppression. With these applications in mind, we recently developed, and describe herein, a tissue-specific qRT-PCR-based protocol for detecting melanoma cells within tumor-draining lymph nodes. Using murine models of lymph-node-invasive and lymph-node-noninvasive melanoma cell lines and a melanin-biosynthesis-pathway-specific <i>Trp2</i> gene expression assay, we validated this method as a highly sensitive strategy for assessing lymph node involvement by melanoma. © 2025 Wiley Periodicals LLC.</p><p><b>Basic Protocol 1</b>: Growth and maintenance of murine melanoma cell cultures</p><p><b>Basic Protocol 2</b>: Extraction and quantification of RNA from murine melanoma cultures</p><p><b>Basic Protocol 3</b>: cDNA synthesis via reverse transcription</p><p><b>Basic Protocol 4</b>: Probe and primer design for TaqMan-based qPCR</p><p><b>Basic Protocol 5</b>: qPCR analysis of tissue-specific <i>Trp2</i> gene expression</p><p><b>Basic Protocol 6</b>: <i>In vitro</i> validation of qRT-PCR <i>Trp2</i> gene expression assay for detection of melanoma cells in murine whole lymph node preparations</p><p><b>Basic Protocol 7</b>: <i>In vivo</i> validation of qRT-PCR <i>Trp2</i> gene expression assay for detection of melanoma cells in murine tumor-draining lymph nodes</p>\",\"PeriodicalId\":93970,\"journal\":{\"name\":\"Current protocols\",\"volume\":\"5 4\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-04-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current protocols\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/cpz1.70139\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current protocols","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpz1.70139","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

黑色素瘤侵袭局部淋巴结是该疾病进展中的关键事件,已被充分证明是黑色素瘤患者预后不良的因素。因此,对于T期≥T2a的黑色素瘤患者,评估淋巴结受累情况是诊断检查的常规部分。在临床环境中,黑色素瘤淋巴结受累的状态和程度传统上是通过前哨淋巴结活检获得的组织病理学分析来表征的,这是一种劳动密集型和昂贵的方法,需要技术上具有挑战性的样本制备和训练有素的病理学家的解释。因此,可以减少财政负担和前哨淋巴结活检检查的周转时间的替代方法是可取的。同样,在实验环境中准确评估黑色素瘤淋巴结侵袭的能力对于获得远端转移和肿瘤相关免疫抑制机制的新见解是必要的。考虑到这些应用,我们最近开发了一种基于组织特异性qrt - pcr的方案,用于检测肿瘤引流淋巴结内的黑色素瘤细胞。通过小鼠淋巴结侵袭性和淋巴结非侵袭性黑色素瘤细胞系模型以及黑色素生物合成途径特异性Trp2基因表达测定,我们验证了该方法是一种高度敏感的评估黑色素瘤淋巴结累及的策略。©2025 Wiley期刊有限公司基本方案1:小鼠黑色素瘤细胞培养的生长和维持基本方案2:从小鼠黑色素瘤培养物中提取和定量RNA基本方案3:通过逆转录合成cDNA基本方案4:基于taqman的qPCR探针和引物设计基本方案5:组织特异性Trp2基因表达的qPCR分析基本方案6:qRT-PCR Trp2基因表达法检测小鼠全淋巴结黑色素瘤细胞的体外验证基本方案7:qRT-PCR Trp2基因表达法检测小鼠肿瘤引流淋巴结黑色素瘤细胞的体内验证
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Highly Sensitive Tissue-specific qRT-PCR-based Assay for Detection of Melanoma Cells in Tumor-Draining Lymph Nodes

Melanoma invasion of regional lymph nodes, a critical event in the progression of this disease, is well documented as a poor prognostic factor for patients with melanoma. Assessing lymph node involvement is therefore a routine part of the diagnostic workup for patients presenting with melanoma at a T stage of ≥T2a. In clinical settings, the status and degree of melanoma lymph node involvement is traditionally characterized by histopathological analysis of tissue obtained during a sentinel lymph node biopsy, a labor-intensive and costly approach that requires technically challenging sample preparation and interpretation by a trained pathologist. Alternative approaches that might reduce the financial burden and turnaround time of a sentinel lymph node biopsy workup are therefore desirable. Likewise, the ability to accurately assess lymph node invasion by melanoma in experimental settings is necessary to gain new insights into mechanisms of distant metastasis and tumor-associated immune suppression. With these applications in mind, we recently developed, and describe herein, a tissue-specific qRT-PCR-based protocol for detecting melanoma cells within tumor-draining lymph nodes. Using murine models of lymph-node-invasive and lymph-node-noninvasive melanoma cell lines and a melanin-biosynthesis-pathway-specific Trp2 gene expression assay, we validated this method as a highly sensitive strategy for assessing lymph node involvement by melanoma. © 2025 Wiley Periodicals LLC.

Basic Protocol 1: Growth and maintenance of murine melanoma cell cultures

Basic Protocol 2: Extraction and quantification of RNA from murine melanoma cultures

Basic Protocol 3: cDNA synthesis via reverse transcription

Basic Protocol 4: Probe and primer design for TaqMan-based qPCR

Basic Protocol 5: qPCR analysis of tissue-specific Trp2 gene expression

Basic Protocol 6: In vitro validation of qRT-PCR Trp2 gene expression assay for detection of melanoma cells in murine whole lymph node preparations

Basic Protocol 7: In vivo validation of qRT-PCR Trp2 gene expression assay for detection of melanoma cells in murine tumor-draining lymph nodes

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
4.00
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信