胰腺癌
生物
癌症的体细胞进化
表型
基础(医学)
人口
腺癌
染色质
病理
背景(考古学)
癌症研究
基因
癌症
遗传学
医学
内分泌学
环境卫生
胰岛素
古生物学
作者
Akimasa Hayashi,Jun Fan,Ruoyao Chen,Yu-Jui Ho,Alvin Makohon‐Moore,Nicolas Lecomte,Yi Zhong,Jungeui Hong,Jinlong Huang,Hitomi Sakamoto,Marc A. Attiyeh,Zachary A. Kohutek,Lance Zhang,Aida Boumiza,Rajya Kappagantula,Priscilla Baez,Jessica Jingyi Bai,Marta Lisi,Kalyani Chadalavada,Jerry P. Melchor
出处
期刊:Nature cancer
[Nature Portfolio]
日期:2020-01-13
卷期号:1 (1): 59-74
被引量:168
标识
DOI:10.1038/s43018-019-0010-1
摘要
Pancreatic cancer expression profiles largely reflect a classical or basal-like phenotype. The extent to which these profiles vary within a patient is unknown. We integrated evolutionary analysis and expression profiling in multiregion-sampled metastatic pancreatic cancers, finding that squamous features are the histologic correlate of an RNA-seq-defined basal-like subtype. In patients with coexisting basal and squamous and classical and glandular morphology, phylogenetic studies revealed that squamous morphology represented a subclonal population in an otherwise classical and glandular tumor. Cancers with squamous features were significantly more likely to have clonal mutations in chromatin modifiers, intercellular heterogeneity for MYC amplification and entosis. These data provide a unifying paradigm for integrating basal-type expression profiles, squamous histology and somatic mutations in chromatin modifier genes in the context of clonal evolution of pancreatic cancer.
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