Detail (Experimental CeRNA)

Home Detail(Experimental CeRNA)

Basic Information

Regular Relationship :


Phenotype/DiseaseSpecie

Melanoma

CeRNA1

PVT1[LncRNA]

miRNA

miR-26b[miRNA]

CeRNA2

NA[mRNA]


Tissue/Cell line

M21, B16F10, Mm200, Mel-Rm, A375, A2058

Specie

Homo sapiens (human)

Citation

Oncol Res 2018 Jun 11 26, 675-681 doi:10.3727/096504017x14920318811730 PMID:28409552


Reference title
Long Noncoding RNA PVT1 Promotes Melanoma Progression Via Endogenous Sponging MiR-26b
Experimental verification
qPCR

Functional description
Expression of PVT1 was significantly up-regulated in melanoma tissue and associated with poor prognosis.Overall,our study demonstrates the oncogenic role of PVT1 as a miR-26b sponge, possibly providing a novel therapeutic target for melanoma

Annotations

External Annotation for PVT1
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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