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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Publication Details

Journal
Stem Cell Reports
Published
2025-09-23
DOI
https://doi.org/10.1016/j.stemcr.2025.102643
Citations
1
Primary Topic
Pluripotent Stem Cells Research
Type
article
Field-Weighted Citation Impact
0.81
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article

Drivers and implications of lineage-specific cancer-related mutations in human pluripotent and adult stem cells

Jonathan Jung, Nissim Benvenisty
1 citations
Stem Cell Reports
Pluripotent Stem Cells Research
0.81
article

Drivers and implications of lineage-specific cancer-related mutations in human pluripotent and adult stem cells

Jonathan Jung, Nissim Benvenisty
article en
1 citations

Abstract

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.

Stem Cell ReportsVol. 20(10)
Hebrew University of Jerusalem (IL), Jerusalem Institute for Israel Studies (IL)
Openalex Percentile: Top 23%
Pluripotent Stem Cells Research
0.81
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