Δευτέρα 4 Μαΐου 2020

MALAT1 Decreases the Sensitivity of Head and Neck Squamous Cell Carcinoma Cells to Radiation and Cisplatin

MALAT1 Decreases the Sensitivity of Head and Neck Squamous Cell Carcinoma Cells to Radiation and Cisplatin:

Background/Aim: Two-thirds of head and neck squamous cell carcinoma (HNSCC) patients present with locally advanced (LA) stages and have a poor survival rate. The aim of this study was to investigate the roles of the long non-coding RNAs MALAT1 on radiation and cisplatin sensitivity of HNSCC cells. Materials and Methods: Clonogenic, cell viability, and apoptosis assays were performed in cells following MALAT1 knockdown using CRISPR/Cas9 system. Results: MALAT1 was overexpressed in HNSCC cell lines as compared to a non-tumorigenic cell line. The number of colonies formed after radiation was significantly reduced in MALAT1 knockdown cells. The IC50 value of cisplatin in MALAT1 knockdown cells was lower than that of the control cells. MALAT1 knockdown resulted in cell cycle arrest at G2/M phase, DNA damage and apoptotic cell death. Conclusion: MALAT1 knockdown enhanced the sensitivity of HNSCC cells to radiation and cisplatin partly through the induction of G2/M cell cycle arrest resulting in DNA damage and apoptosis.



MALAT1 metastasis associated lung adenocarcinoma transcript 1 [ Homo sapiens (human) ]

Gene ID: 378938, updated on 3-May-2020

Summary


Official Symbol
MALAT1provided by HGNC
Official Full Name
metastasis associated lung adenocarcinoma transcript 1provided by HGNC
Primary source
HGNC:HGNC:29665
See related
Ensembl:ENSG00000251562 MIM:607924
Gene type
ncRNA
RefSeq status
REVIEWED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
HCN; NEAT2; PRO2853; LINC00047; NCRNA00047
Summary
This gene produces a precursor transcript from which a long non-coding RNA is derived by RNase P cleavage of a tRNA-like small ncRNA (known as mascRNA) from its 3' end. The resultant mature transcript lacks a canonical poly(A) tail but is instead stabilized by a 3' triple helical structure. This transcript is retained in the nucleus where it is thought to form molecular scaffolds for ribonucleoprotein complexes. It may act as a transcriptional regulator for numerous genes, including some genes involved in cancer metastasis and cell migration, and it is involved in cell cycle regulation. Its upregulation in multiple cancerous tissues has been associated with the proliferation and metastasis of tumor cells. [provided by RefSeq, Mar 2015]
Expression
Ubiquitous expression in bone marrow (RPKM 137.2), thyroid (RPKM 115.3) and 24 other tissues See more
Orthologs

Genomic context

See MALAT1 in Genome Data Viewer
Location:
 
11q13.1
Exon count:
 
2
Annotation releaseStatusAssemblyChrLocation
109.20200228currentGRCh38.p13 (GCF_000001405.39)11NC_000011.10 (65497738..65506516)
105previous assemblyGRCh37.p13 (GCF_000001405.25)11NC_000011.9 (65265224..65273940)
Chromosome 11 - NC_000011.10Genomic Context describing neighboring genesNeighboring gene CRISPRi-validated cis-regulatory element chr11.3251Neighboring gene ZFP161 motif-containing MPRA enhancer 21/22Neighboring gene TALAM1 transcript, MALAT1 antisense RNANeighboring gene MALAT1-associated small cytoplasmic RNANeighboring gene small nuclear ribonucleoprotein polypeptide G pseudogene 19Neighboring gene SCY1 like pseudokinase 1Neighboring gene latent transforming growth factor beta binding protein 3

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018
adrenalappendixbone marrowbraincolonduodenumendometriumesophagusfatgall bladderheartkidneyliverlunglymph nodeovarypancreasplacentaprostatesalivary glandskinsmall intestinespleenstomachtestisthyroidurinary bladder0255075100125150175200SamplesRPKM

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Phenotypes

NHGRI GWAS Catalog

Description
Genome-wide association study identifies three novel susceptibility loci for severe Acne vulgaris.
NHGRI GWA Catalog

Interactions

General gene information

Homology

Other Names

  • hepcarcin
  • long intergenic non-protein coding RNA 47
  • metastasis associated lung adenocarcinoma transcript 1 (non-protein coding)
  • nuclear enriched abundant transcript 2
  • nuclear paraspeckle assembly transcript 2 (non-protein coding)

NCBI Reference Sequences (RefSeq)

RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

RNA

  1. NR_002819.4 RNA Sequence
    Status: REVIEWED
    Description
    Transcript Variant: This variant (1) represents the unspliced, longest transcript.
    Source sequence(s)
    AI805768, CA394984, EF177381
    Related
    ENST00000534336.1

  2. NR_144567.1 RNA Sequence
    Status: REVIEWED
    Description
    Transcript Variant: This variant (2, also known as long) lacks an alternate segment in the 5' region compared to variant 1.
    Source sequence(s)
    AI805768, BK001418, CA394984, EF177381

  3. NR_144568.1 RNA Sequence
    Status: REVIEWED
    Description
    Transcript Variant: This variant (3, also known as short) lacks two alternate segments compared to variant 1.
    Source sequence(s)
    AI805768, BK001411, CA394984, EF177381

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000011.10 Reference GRCh38.p13 Primary Assembly
    Range
    65497738..65506516
    Download
    GenBankFASTASequence Viewer (Graphics)

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