General Information of the Molecule (ID: Mol01718)
Name
hsa-miR-423-5p ,Homo sapiens
Synonyms
microRNA 423
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Molecule Type
Mature miRNA
Sequence
UGAGGGGCAGAGAGCGAGACUUU
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Ensembl ID
ENSG00000283935
HGNC ID
HGNC:31880
Mature Accession
MIMAT0004748
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Kingdom: Metazoa
Phylum: Chordata
Class: Mammalia
Order: Primates
Family: Hominidae
Genus: Homo
Species: Homo sapiens
Type(s) of Resistant Mechanism of This Molecule
  EADR: Epigenetic Alteration of DNA, RNA or Protein
Drug Resistance Data Categorized by Drug
Approved Drug(s)
2 drug(s) in total
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Cisplatin
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Drug Resistance Data Categorized by Their Corresponding Mechanisms
  Epigenetic Alteration of DNA, RNA or Protein (EADR) Click to Show/Hide
Disease Class: Non-small cell lung cancer [ICD-11: 2C25.0] [1]
Resistant Disease Non-small cell lung cancer [ICD-11: 2C25.0]
Resistant Drug Cisplatin
Molecule Alteration Expression
Up-regulation
Experimental Note Revealed Based on the Cell Line Data
In Vitro Model H446 cells Lung Homo sapiens (Human) CVCL_1562
H446 cells Lung Homo sapiens (Human) CVCL_1562
Experiment for
Molecule Alteration
qPCR
Experiment for
Drug Resistance
MTT assay
Mechanism Description This gene is up-regulated in cisplatin-resistance cells
Temozolomide
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Drug Resistance Data Categorized by Their Corresponding Mechanisms
  Epigenetic Alteration of DNA, RNA or Protein (EADR) Click to Show/Hide
Disease Class: Glioblastoma [ICD-11: 2A00.02] [2]
Resistant Disease Glioblastoma [ICD-11: 2A00.02]
Resistant Drug Temozolomide
Molecule Alteration Expression
Up-regulation
Experimental Note Revealed Based on the Cell Line Data
Cell Pathway Regulation AKT/ERK signaling pathway Activation hsa04010
Cell invasion Activation hsa05200
Cell proliferation Activation hsa05200
In Vitro Model U251 cells Brain Homo sapiens (Human) CVCL_0021
U87 cells Brain Homo sapiens (Human) CVCL_0022
N3 GBM cells Brain Homo sapiens (Human) N.A.
Experiment for
Molecule Alteration
RT-PCR; qRT-PCR
Experiment for
Drug Resistance
Cell-cycle assay
Mechanism Description miR-423-5p contributes to a malignant phenotype and temozolomide chemoresistance in glioblastomas.
Investigative Drug(s)
1 drug(s) in total
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Apigenin
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Drug Sensitivity Data Categorized by Their Corresponding Mechanisms
  Epigenetic Alteration of DNA, RNA or Protein (EADR) Click to Show/Hide
Disease Class: Glioma [ICD-11: 2A00.1] [3]
Sensitive Disease Glioma [ICD-11: 2A00.1]
Sensitive Drug Apigenin
Molecule Alteration Expression
Down-regulation
Experimental Note Revealed Based on the Cell Line Data
Cell Pathway Regulation Bax/BCL2/caspase-3 signaling pathway Activation hsa04933
Mitochondrial signaling pathway Regulation N.A.
In Vitro Model CD133-positive cells Brain Homo sapiens (Human) CVCL_IR55
Experiment for
Molecule Alteration
qRT-PCR
Experiment for
Drug Resistance
MTT assay; Annexin V/PI apoptosis assay; Caspase-3 activity assay
Mechanism Description Retracted-miR423-5p knockdown enhances the sensitivity of glioma stem cells to apigenin through the mitochondrial pathway.
References
Ref 1 Altiratinib Inhibits Tumor Growth, Invasion, Angiogenesis, and Microenvironment-Mediated Drug Resistance via Balanced Inhibition of MET, TIE2, and VEGFR2Mol Cancer Ther. 2015 Sep;14(9):2023-34. doi: 10.1158/1535-7163.MCT-14-1105. Epub 2015 Aug 18.
Ref 2 miR-423-5p contributes to a malignant phenotype and temozolomide chemoresistance in glioblastomas. Neuro Oncol. 2017 Jan;19(1):55-65. doi: 10.1093/neuonc/now129. Epub 2016 Jul 28.
Ref 3 miR-423-5p knockdown enhances the sensitivity of glioma stem cells to apigenin through the mitochondrial pathway. Tumour Biol. 2017 Apr;39(4):1010428317695526. doi: 10.1177/1010428317695526.

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