人群间癌症差异的转化研究项目。

Jane C Figueiredo, Diana Redwood, Li Li, Elizabeth Donato, Daniel Fort, Eric E Fox, William M Grady, Heather Green, Tabitha A Harrison, Carl Haupt, Li Hsu, Meredith A J Hullar, Jeroen R Huyghe, Wenora Johnson, Amanda L Koehne, Scott D LaBrie, Meredith A Lakey, MingGang Lin, Nicole C Loroña, Grace A Maresh, Marc Matrana, Jonathan D Mizrahi, Sarah H Nash, Nathalie T Nguyen, Jennifer L Paruch, Amanda I Phipps, Conghui Qu, Timothy W Randolph, Stephanie Romo, Claire E Thomas, Sushma Thomas, James Tiesinga, Charles Whitlow, Cecilia C S Yeung, Hang Yin, Craig M Zibilich, Christopher I Li, Timothy K Thomas, Ulrike Peters
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引用次数: 0

摘要

背景:结直肠癌(CRC)的发病率和死亡率在不同人群中差异很大。跨人群癌症差异转化研究计划(TRPCDP)成立于2020年,旨在解决美国境内CRC发病率和死亡率的差异。方法:TRPCDP集中了美国三个站点的数据采集和协调,在四个人群(非裔美国人/黑人、阿拉斯加原住民、西班牙裔/拉丁裔/黑人和非西班牙裔白人)中创建了一个注释良好的结直肠癌肿瘤资源。使用病例-对照框架,将致命性CRC患者与两名非致命性CRC患者相匹配。取经福尔马林固定石蜡包埋的肿瘤组织和正常组织进行集中病理检查,提取DNA和RNA,开发组织芯片。多组学和空间分析正在进行中,以评估转录组、蛋白质组和微生物组。患者人口统计和临床数据通过医疗记录审查、患者自我报告或与癌症登记处的联系获得。利用地理空间联系评估了其他与健康相关的因素。结果:虚拟生物库包括7181名患者[非裔美国人(n=1,345),阿拉斯加原住民(n=1,640),西班牙裔(n=1,659)和非西班牙裔白人(n=2,537)]。938例患者选择组织块(肿瘤1594例,正常结肠728例)。迄今为止,已经提取了DNA和RNA (n=831),并构建了组织微阵列(n=414)。转录组学,空间肿瘤分析(多重免疫荧光,PhenoCycler, GeoMx)和微生物组数据(16S rRNAseq, ddPCR)可用。结论:TRPCDP为未来的分子流行病学研究提供了临床注释的生物库。影响:TRPCDP是一个独特的项目,支持下一代科学家的合作研究、社区参与和管道开发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Translational Research Program in Cancer Differences across Populations.

Background: Colorectal cancer (CRC) incidence and mortality vary substantially across populations. The Translational Research Program in Cancer Differences across Populations (TRPCDP) was established in 2020 to address differences in CRC incidence and mortality rates within the United States.

Methods: TRPCDP centralized data acquisition and harmonization across three sites in the U.S. to create a well-annotated resource of CRC tumors across four populations: African American/Black, Alaska Native, Hispanic/Latino/a, and non-Hispanic White. Using a case-control framework, patients with lethal CRC were matched to two controls with non-lethal CRC. Formalin-fixed paraffin-embedded tumor and normal tissue were retrieved and sent for centralized pathology review, followed by DNA and RNA extraction and tissue microarray development. Multi-omics and spatial profiling are underway to evaluate the transcriptome, proteome, and microbiome. Patient demographic and clinical data were obtained by medical record review, patient self-report, or linkage to cancer registries. Additional health-related factors were assessed using geospatial linkage.

Results: The virtual biorepository includes 7,181 patients [African American (n=1,345), Alaska Native (n=1,640), Hispanic (n=1,659), and non-Hispanic White (n=2,537)]. Tissue blocks (1,594 tumor, 728 normal colon) were selected for 938 patients. To date, DNA and RNA have been extracted (n=831) and tissue microarrays have been constructed (n=414). Transcriptomic, spatial tumor profiling (multiplex immunofluorescence, PhenoCycler, GeoMx) and microbiome data (16S rRNAseq, ddPCR) are available.

Conclusion: The TRPCDP has developed a clinically annotated biorepository for future molecular epidemiology studies.

Impact: TRPCDP is a unique program that supports collaborative research, community engagement, and pipeline development for the next generation of scientists.

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