人类多能干细胞和成体干细胞中谱系特异性癌症相关突变的驱动因素和影响。

IF 5.1 2区 医学 Q1 CELL & TISSUE ENGINEERING
Jonathan Jung, Nissim Benvenisty
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引用次数: 0

摘要

众所周知,人类多能干细胞(PSCs)在肿瘤相关基因中存在突变,在这里,我们的目标是研究成体干细胞(ASCs)的状态。因此,我们在大约600个间充质干细胞样本中发现了18%的癌症相关突变,在大约200个神经干细胞(NSC)样本中发现了41%的癌症相关突变。我们展示了癌症相关基因的谱系特异性谱,证明TP53是人类PSCs的中心突变基因,而不是间充质细胞或NSCs。我们认为,肿瘤相关基因的谱系特异性与其表达水平和患者肿瘤特异性突变相关。我们还展示了癌基因和肿瘤抑制基因突变对每个特定干细胞谱系转录组的影响。因此,我们建议对这些突变样本进行分类,以进一步了解其严重程度,并强调在多能系和ASC系中进行遗传筛查的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Drivers and implications of lineage-specific cancer-related mutations in human pluripotent and adult stem cells.

Human pluripotent stem cells (PSCs) are known to harbor mutations in tumor-associated genes, and here we aim to examine the status of adult stem cells (ASCs). We thus identify cancer-related mutations in 18% of about 600 mesenchymal stem cell samples, and in 41% of about 200 neural stem cell (NSC) samples. We show a lineage-specific profile of cancer-related genes, demonstrating that TP53 is a central mutated gene in human PSCs but not in mesenchymal or NSCs. We suggest that the lineage-specificity of tumor-associated genes correlates with their expression levels and with tumor-specific mutations in patients. We also show the consequences of mutations in oncogenes and tumor suppressor genes on the transcriptome of each specific stem cell lineage. We therefore propose a categorization of these mutated samples for further appreciation of their severity and emphasize the importance of genetic screening in pluripotent and ASC lines.

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来源期刊
Stem Cell Reports
Stem Cell Reports CELL & TISSUE ENGINEERING-CELL BIOLOGY
CiteScore
10.50
自引率
1.70%
发文量
200
审稿时长
28 weeks
期刊介绍: Stem Cell Reports publishes high-quality, peer-reviewed research presenting conceptual or practical advances across the breadth of stem cell research and its applications to medicine. Our particular focus on shorter, single-point articles, timely publication, strong editorial decision-making and scientific input by leaders in the field and a "scoop protection" mechanism are reasons to submit your best papers.
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