Transcriptomics

Dataset Information

0

Transforming pluripotency: an exon-level study of malignancy-specific transcripts in human embryonal carcinoma and embryonic stem cells


ABSTRACT: Exon-level transcriptome analysis of embryonal carcinoma (EC) and embryonic stem (ES) cell lines. To circumvent difficulties of isolating pure populations of cancer stem cells for the purpose of identifying malignancy-specific gene expression, we have compared exon-resolution transcriptomic profiles of five embryonal carcinoma (EC) cell lines, a histological subtype of germ cell tumour, to their non-malignant caricature, specifically six human embryonic stem (ES) cell lines. Both cell types are readily accessible, and were purified for undifferentiated cells only. We identified a set of 28 differentially expressed genes, many of which had cancer and stemness roles. Overexpression of the recently discovered pluripotency gene NR5A2 in malignant EC cells revealed an intriguing indication of how WNT-mediated dysregulation of pluripotency is involved with malignancy. At the exon-level, alternative splicing events were detected in ZNF195, DNMT3B and PMF1, and alternative promoters were detected for ASH2L and ETV5. These events were validated by RT-PCR-based methods in EC and ES lines, and further explored within a series of 25 primary tumours, where the alternative splicing event in the de novo DNA methyltransferase DNMT3B may have functional consequences. In conclusion, we have identified malignancy-specific gene expression differences within a rigorous pluripotent stem cell context. These findings are of particular interest for both germ cell tumour and ES cell biology, and in general to the concept of cancer stem cells.

ORGANISM(S): Homo sapiens

PROVIDER: GSE34855 | GEO | 2015/01/01

SECONDARY ACCESSION(S): PRJNA150117

REPOSITORIES: GEO

Dataset's files

Source:
Action DRS
Other
Items per page:
1 - 1 of 1

Similar Datasets

2015-01-01 | E-GEOD-34855 | biostudies-arrayexpress
2012-12-01 | E-GEOD-42644 | biostudies-arrayexpress
2012-12-01 | E-GEOD-42646 | biostudies-arrayexpress
2017-03-07 | GSE95746 | GEO
2017-03-07 | GSE95745 | GEO
2017-03-07 | GSE95744 | GEO
2017-03-07 | GSE95743 | GEO
2005-12-29 | GSE3921 | GEO
2007-10-26 | GSE4809 | GEO
2012-12-01 | E-GEOD-42645 | biostudies-arrayexpress