甲状腺癌
肿瘤微环境
基质
恶性肿瘤
免疫疗法
间质细胞
生物
甲状腺乳突癌
癌症
肿瘤科
医学
生物信息学
计算生物学
癌症研究
病理
内科学
免疫组织化学
作者
George Xu,Matthew A. Loberg,Jean‐Nicolas Gallant,Quanhu Sheng,Sheau‐Chiann Chen,Brian D. Lehmann,Sophia M. Shaddy,Megan L. Tigue,Courtney J. Phifer,Li Wang,Mario W. Saab‐Chalhoub,Lauren M. Dehan,Qiang Wei,Rui Chen,Bingshan Li,Christine Y Kim,Donna C. Ferguson,James L. Netterville,Sarah L. Rohde,Carmen C. Solórzano
出处
期刊:Cell genomics
[Elsevier]
日期:2023-09-15
卷期号:3 (10): 100409-100409
被引量:21
标识
DOI:10.1016/j.xgen.2023.100409
摘要
Genomic and transcriptomic analysis has furthered our understanding of many tumors. Yet, thyroid cancer management is largely guided by staging and histology, with few molecular prognostic and treatment biomarkers. Here, we utilize a large cohort of 251 patients with 312 samples from two tertiary medical centers and perform DNA/RNA sequencing, spatial transcriptomics, and multiplex immunofluorescence to identify biomarkers of aggressive thyroid malignancy. We identify high-risk mutations and discover a unique molecular signature of aggressive disease, the Molecular Aggression and Prediction (MAP) score, which provides improved prognostication over high-risk mutations alone. The MAP score is enriched for genes involved in epithelial de-differentiation, cellular division, and the tumor microenvironment. The MAP score also identifies aggressive tumors with lymphocyte-rich stroma that may benefit from immunotherapy. Future clinical profiling of the stromal microenvironment of thyroid cancer could improve prognostication, inform immunotherapy, and support development of novel therapeutics for thyroid cancer and other stroma-rich tumors.
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