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Integrative analysis of transcription factors and microRNAs in ovarian cancer cell spheroids.


ABSTRACT: BACKGROUND:Cancer stem cells (CSCs) can self-renew, proliferate into differentiated cells, or enter a quiescent state and are regarded to cause chemoresistance and recurrence. An integrative analysis of transcription factors (TF) and miRNAs was performed in ovarian CSC-enriched spheroid-forming cells (SFCs) to identify factors relevant to ovarian CSCs. METHODS:Fresh tumor cells from three ovarian cancer patients were cultured in standard and in selective medium. The mRNAs and miRNAs that exhibited significant differential expression between SFCs and adherent cells were identified using mRNA and miRNAs microarrays. Target genes of miRNAs were further selected if predicted with TargetScan by half of the miRNAs or more. Gene enrichment analysis was performed on over- or under-expressed mRNAs and target genes of miRNAs using DAVID tools. Complex regulatory networks were combined from TF-genes and miRNA-genes interactions using the MAGIA webtool. RESULTS:A total of 1245 mRNA and 55 miRNAs were differentially expressed (p-value

SUBMITTER: Park H 

PROVIDER: S-EPMC7014770 | biostudies-literature | 2020 Feb

REPOSITORIES: biostudies-literature

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Integrative analysis of transcription factors and microRNAs in ovarian cancer cell spheroids.

Park Hyun H   Hwang Sohyun S   Jeong Ju-Yeon JY   Jung Sang Geun SG   Choi Min Chul MC   Joo Won Duk WD   Song Seung Hun SH   Lee Chan C   An Hee Jung HJ  

Journal of ovarian research 20200211 1


<h4>Background</h4>Cancer stem cells (CSCs) can self-renew, proliferate into differentiated cells, or enter a quiescent state and are regarded to cause chemoresistance and recurrence. An integrative analysis of transcription factors (TF) and miRNAs was performed in ovarian CSC-enriched spheroid-forming cells (SFCs) to identify factors relevant to ovarian CSCs.<h4>Methods</h4>Fresh tumor cells from three ovarian cancer patients were cultured in standard and in selective medium. The mRNAs and miRN  ...[more]

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