Detail (Experimental CeRNA)

Home Detail(Experimental CeRNA)

Basic Information

Regular Relationship :


Phenotype/DiseaseSpecie

Hepatocellular Carcinoma

CeRNA1

MEG3[LncRNA]

miRNA

miR-9-5p[miRNA]

CeRNA2

SOX11[mRNA]


Tissue/Cell line

Human embryonic kidney cell line (293T) and Human HCC cell lines (SK-HEP-1 and Huh7)

Specie

Homo sapiens (human)

Citation

Braz J Med Biol Res 2019 52, e8631 doi:10.1590/1414-431x20198631 PMID:31531526


Reference title
lncRNA MEG3 inhibits the growth of hepatocellular carcinoma cells by sponging miR-9-5p to upregulate SOX11
Experimental verification
qRT-PCR,Western blot,Flow cytometry etc.

Functional description
In the present study, we determined the expression of MEG3, miR-9-5p, and SOX11 in HCC tissues, and explored their interactions in HCC. Furthermore, we detected the effect of these molecules on HCC cell growth and apoptosis.

Annotations

External Annotation for MEG3
LncRNA-associated competing triplets and functions.
Comprehensive experimentally supported associations between lncRNA and human cancer.
Infer genomic variations that disturb lncRNA-associated ceRNA regulation..
Provide and annotate disease or phenotype-associated variants in human long non-coding RNAs (lncRNAs) and circular RNAs (circRNAs) or their regulatory elements.
Providing cellular-specific lncRNA-associated ceRNA networks predicted via high-throughput analysis of single-cell genomic data.
Information on all annotated and predicted human genes.
Gene nomenclature, gene families and associated resources (genomic, proteomic, phenotypic information).
Genome browser for vertebrate genomes.
An annotated collection of all publicly available DNA sequences.
A wiki-based platform for community curation of human long non-coding RNAs.
An integrated knowledge database dedicated to non-coding RNAs.
An integrated database of human annotated lncRNA transcripts.
Comprehensive annotations of eukaryotic long non-coding RNAs.
Comprehensive experimentally supported associations between lncRNA and human cancer.
A comprehensive, authoritative compendium of human genes and genetic phenotypes.
The catalogue of somatic mutations in cancer.

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