免疫系统
生物
腺癌
计算生物学
遗传学
进化生物学
癌症
作者
Yue Zhao,Jian Gao,Jun Wang,Fanfan Fan,Chao Cheng,Danwen Qian,Ran Guo,Yang Zhang,Ting Ye,Marcellus Augustine,Yicong Lin,Jun Shang,Hang Li,Yunjian Pan,Qingyuan Huang,Haiqing Chen,Han Han,Zhendong Gao,Qiming Wang,Shiyue Zhang
标识
DOI:10.1038/s41467-024-52139-2
摘要
Multiple synchronous lung cancers (MSLCs) constitute a unique subtype of lung cancer. To explore the genomic and immune heterogeneity across different pathological stages of MSLCs, we analyse 16 MSLCs from 8 patients using single-cell RNA-seq, single-cell TCR sequencing, and bulk whole-exome sequencing. Our investigation indicates clonally independent tumours with convergent evolution driven by shared driver mutations. However, tumours from the same individual exhibit few shared mutations, indicating independent origins. During the transition from pre-invasive to invasive adenocarcinoma, we observe a shift in T cell phenotypes characterized by increased Treg cells and exhausted CD8
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