Unknown,Transcriptomics,Genomics,Proteomics

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Profiling and Functional Analyses of MicroRNAs and Their Target Gene Products in Human Uterine Leiomyomas


ABSTRACT: Human uterine leiomyomas (ULM) are characterized by dysregulation of a large number of genes and non-coding regulatory microRNAs. In order to identify microRNA::mRNA associations relevant to ULM pathogenesis, we examined global correlation patterns between the altered microRNA expression and the predicted target genes in leiomyomas and matched myometria. We found that some but not all of the predicted and inversely correlated target genes in ULMs can be directly regulated by microRNAs in vitro. Our findings provide a broad overview of molecular events underlying the tumorigenesis of uterine leiomyoma and identify select genetic and regulatory events that alter microRNA expression and may play important roles in ULM pathobiology by positively regulating tumor growth while maintaining the non-invasive character of ULMs Keywords: Differential gene expression Paired normal (myometrium) and tumor (ULM) samples derived from 5 patients were used

ORGANISM(S): Homo sapiens

SUBMITTER: Jiri Zavadil 

PROVIDER: E-GEOD-23112 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Profiling and functional analyses of microRNAs and their target gene products in human uterine leiomyomas.

Zavadil Jiri J   Ye Huihui H   Liu Zhaojian Z   Wu JingJing J   Lee Peng P   Hernando Eva E   Soteropoulos Patricia P   Toruner Gokce A GA   Wei Jian-Jun JJ  

PloS one 20100824 8


<h4>Background</h4>Human uterine leiomyomas (ULM) are characterized by dysregulation of a large number of genes and non-coding regulatory microRNAs. In order to identify microRNA::mRNA associations relevant to ULM pathogenesis, we examined global correlation patterns between the altered microRNA expression and the predicted target genes in ULMs and matched myometria.<h4>Methodology/principal findings</h4>Patterns of inverse association of microRNA with mRNA expression in ULMs revealed an involve  ...[more]

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