Detail (Experimental CeRNA)

Home Detail(Experimental CeRNA)

Basic Information

Regular Relationship :


Phenotype/DiseaseSpecie

Tongue Squamous Cell Carcinoma

CeRNA1

UCA1[LncRNA]

miRNA

miR-138-5p[miRNA]

CeRNA2

CCR7[mRNA]


Tissue/Cell line

TSCC cell lines (SCC4, SCC15, SCC25 and CAL-27)

Specie

Homo sapiens (human)

Citation

Neoplasma 2020 Nov 67, 1256-1265 doi:10.4149/neo_2020_191119N1187 PMID:32749849


Reference title
Long noncoding RNA UCA1 regulates CCR7 expression to promote tongue squamous cell carcinoma progression by sponging miR-138-5p.
Experimental verification
qRT-PCR,Western blot,Luciferase reporter assay etc.

Functional description
In summary, we concluded that UCA1 played an oncogenic role in TSCC through regulating the miR-138-5p/CCR7 axis, which provided a reliable biomarker for the clinical treatment of TSCC.

Annotations

External Annotation for UCA1
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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