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Dataset: Expression data from diploid and aneuoploid human pluripotent stem cells, teratomas derived from them, and pluripotent-like cells recovered from these teratomas

Human pluripotent stem cells (hPSCs) tend to acquire genomic aberrations in culture, the most common of which is the trisomy of...

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Human pluripotent stem cells (hPSCs) tend to acquire genomic aberrations in culture, the most common of which is the trisomy of chromosome 12. Interestingly, trisomy 12 is also prevalent in germ cell tumors (GCTs). Here, we aimed to dissect the cellular and molecular implications of trisomy 12 in hPSCs. A genome-wide gene expression analysis revealed that trisomy 12 profoundly affects the global gene expression profile of hPSCs, inducing a transcriptional program very similar to that of CGTs. Direct comparison of the proliferation, replication, differentiation and apoptosis between diploid and aneuploid hPSCs revealed that trisomy 12 significantly increases the proliferation rate of hPSCs. Increased replication largely accounts for the increased proliferation observed, and may explain the selection advantage that trisomy 12 confers to hPSCs. A comparison of the tumors induced by diploid and aneuploid hPSCs further demonstrated that trisomy 12 increases the tumorigenicity of hPSCs, inducing transcriptionally-distinct teratomas, from which pluripotent cells can be recovered. Lastly, a chemical screen of 89 anticancer drugs against diploid and aneuploid hPSCs discovered that trisomy 12 raises the sensitivity of hPSCs to several replication inhibitors, suggesting that the increased proliferation and tumorigenicity of these aberrant cells also makes them more vulnerable, and might potentially be used for their selective elimination from culture. Together, our findings demonstrate the extensive effect of trisomy 12 on the gene expression signature and on the cellular behavior of hPSCs, and highlight the danger posed by this trisomy for the successful use of hPSCs in basic research and in regenerative medicine. Expression data from diploid and aneuoploid human pluripotent stem cells, teratomas derived from them, and pluripotent-like cells recovered from these teratomas total RNA was isolated from undifferentiated human pluripotent stem cells grown under standard human ES conditions, or from teratomas derived from them, or from ES-like cells recovered from these teratomas.

Species:
human

Samples:
13

Source:
E-GEOD-51455

Updated:
Dec.12, 2014

Registered:
Sep.21, 2014


Factors: (via ArrayExpress)
Sample CELL LINE PASSAGE GENOTYPE CELL TYPE
GSM1246010 CSES22 passage 34 47(X,X, +12) Undifferentiated human embryonic stem cells
GSM12460 CSES45 passage 22 47(X,X, +12) Undifferentiated human embryonic stem cells
GSM1246012 CSES7 passage 52 46(X,X) In-vivo differentiated human embryonic stem cells
GSM1246013 CSES15 passage 52 46(X,X) In-vivo differentiated human embryonic stem cells
GSM1246014 CSES25 passage 52 46(X,X) In-vivo differentiated human embryonic stem cells
GSM1246015 CSES26 passage 35 46(X,X) In-vivo differentiated human embryonic stem cells
GSM1246016 HiPS18 passage 35 47(X,Y, +12) In-vivo differentiated human induced pluripotent stem cells
GSM1246017 CSES22 not specified 47(X,X, +12) In-vivo differentiated human embryonic stem cells
GSM1246018 CSES45 not specified 47(X,X, +12) In-vivo differentiated human embryonic stem cells
GSM1246019 HiPS18 not specified 47(X,Y, +12) In-vivo differentiated human induced pluripotent stem cells
GSM1246020 CSES22 not specified 47(X,X, +12) Undifferentiated human embryonic stem cells recovered from teratoma
GSM124602 HiPS18 not specified 47(X,Y, +12) Undifferentiated human induced pluripotent stem cells recovered from teratoma
GSM124602 HiPS18 not specified 47(X,Y, +12) Undifferentiated human induced pluripotent stem cells recovered from teratoma

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  • cell
  • chromosome
  • genome

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