当前位置:科学网首页 > 小柯机器人 >详情
汤富酬/付卫合作揭示结直肠癌的普遍基因组改变
作者:小柯机器人 发布时间:2020/10/25 22:01:18

北京大学汤富酬、付卫等研究人员合作利用单细胞多组学测序,揭示出人类结直肠癌肿瘤基质细胞中普遍的基因组改变。这一研究成果于2020年10月22日在线发表在国际学术期刊《癌细胞》上。

研究人员表示,肿瘤微环境(TME)中的基质细胞被结直肠癌(CRC)转化到何种程度尚未得到研究。
 
为了剖析这些非恶性细胞的变化,研究人员对21例微卫星稳定的CRC和6名无癌的老年患者进行了单细胞多组学测序。令人惊讶的是,体细胞拷贝数改变(SCNA)在TME和每位个体正常组织中的免疫细胞、成纤维细胞和内皮细胞中普遍存在。此外,肿瘤中SCNA的成纤维细胞比例(11.1%–47.7%)远高于邻近正常组织的比例(1.1%–10.6%),其中第7号染色体的增益显著富集在TME中,并清楚地表明了克隆扩增。
 
此外,五个基因(BGN、RCN3、TAGLN、MYL9和TPM2)被鉴定为成纤维细胞特异性的生物标志物,其预后较差。这项研究提供了CRC中TME基质细胞中普遍基因组改变的证据和功能相关性。
 
附:英文原文

Title: Single-Cell Multiomics Sequencing Reveals Prevalent Genomic Alterations in Tumor Stromal Cells of Human Colorectal Cancer

Author: Yuan Zhou, Shuhui Bian, Xin Zhou, Yueli Cui, Wendong Wang, Lu Wen, Limei Guo, Wei Fu, Fuchou Tang

Issue&Volume: 2020-10-22

Abstract: To what extent stromal cells in the tumor microenvironment (TME) are transformed bycolorectal cancer (CRC) cells is unexplored. To dissect alterations in these non-malignantcells, we performed single-cell multiomics sequencing of 21 patients with microsatellite-stableCRCs and 6 cancer-free, elderly individuals. Surprisingly, somatic copy number alterations(SCNAs) are prevalent in immune cells, fibroblasts, and endothelial cells in boththe TME and the normal tissues of each individual. Moreover, the proportions of fibroblastswith SCNAs in tumors (11.1%–47.7%) are much higher than those in adjacent normal tissues(1.1%–10.6%), with gain of chromosome 7 strongly enriched in the TME, clearly indicatingclonal expansion. Furthermore, five genes (BGN, RCN3, TAGLN, MYL9, and TPM2) are identified as fibroblast-specific biomarkers of poorer prognosis of CRC. Ourstudy provides evidence and functional relevance of pervasive genomic alterationsin the stromal cells of TME in CRC.

DOI: 10.1016/j.ccell.2020.09.015

Source: https://www.cell.com/cancer-cell/fulltext/S1535-6108(20)30489-X

期刊信息

Cancer Cell:《癌细胞》,创刊于2002年。隶属于细胞出版社,最新IF:23.916
官方网址:https://www.cell.com/cancer-cell/home
投稿链接:https://www.editorialmanager.com/cancer-cell/default.aspx