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Single-cell sequencing reveals the potential oncogenic expression atlas of human iPSC-derived cardiomyocytes
Journal article   Open access   Peer reviewed

Single-cell sequencing reveals the potential oncogenic expression atlas of human iPSC-derived cardiomyocytes

Minglin Ou, Min Zhao, Chunhong Li, Donge Tang, Yong Xu, Weier Dai, Weiguo Sui, Yue Zhang, Zhen Xiang, Chune Mo, …
Biology Open, Vol.10(2), bio053348
2021
PMCID: PMC7903994
PMID: 33589441
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Single-cell sequencing reveals the potential oncogenic expression atlas of human iPSC-derived cardiomyocytes3.68 MBDownloadView
Published Version Open Access CC BY V4.0
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https://doi.org/10.1242/bio.053348View
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Abstract

Single-cell transcriptomics TP53 MYC Oncogene Tumor suppressor gene
Human induced pluripotent stem cells (iPSCs) are important source for regenerative medicine. However, the links between pluripotency and oncogenic transformation raise safety issues. To understand the characteristics of iPSC-derived cells at single-cell resolution, we directly reprogrammed two human iPSC lines into cardiomyocytes and collected cells from four time points during cardiac differentiation for single-cell sequencing. We captured 32,365 cells and identified five molecularly distinct clusters that aligned well with our reconstructed differentiation trajectory. We discovered a set of dynamic expression events related to the upregulation of oncogenes and the decreasing expression of tumor suppressor genes during cardiac differentiation, which were similar to the gain-of-function and loss-of-function patterns during oncogenesis. In practice, we characterized the dynamic expression of the

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