General Information of the Molecule (ID: Mol05124)
Name
hsa-miR-363-3p ,Homo sapiens
Molecule Type
Mature miRNA
Sequence
AAUUGCACGGUAUCCAUCUGUA
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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)
1 drug(s) in total
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Fluorouracil
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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: Breast cancer [ICD-11: 2C60.2] [1]
Resistant Disease Breast cancer [ICD-11: 2C60.2]
Resistant Drug Fluorouracil
Molecule Alteration Expression
Up-regulation
Experimental Note Identified from the Human Clinical Data
Experiment for
Molecule Alteration
RT-PCR
Mechanism Description Hsa-miR-363-3p expression is significantly upregulated in 5-Fluorouracil (5-FU)-resistant breast cancer stem cell (BCSC)-enriched mammospheres compared to non-resistant adherent cells or non-tumorigenic cells, and its high expression contributes to 5-FU chemoresistance by maintaining BCSC stemness and tumorigenicity.
Clinical Trial Drug(s)
1 drug(s) in total
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PLX4720
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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: Papillary thyroid carcinoma [ICD-11: 2D10.1] [2]
Resistant Disease Papillary thyroid carcinoma [ICD-11: 2D10.1]
Resistant Drug PLX4720
Molecule Alteration Expression
Up-regulation
Experimental Note Revealed Based on the Cell Line Data
Experiment for
Molecule Alteration
Immunoblot analysis; qRT-PCR
Experiment for
Drug Resistance
Flow cytometry assay
Mechanism Description This gene is up-regulated in PLX4720-resistance cells
References
Ref 1 miR-363-3p Mediates Maintenance and Tumorigenicity of Breast Cancer Stem Cells and Provides A Potential Diagnostic and Prognostic Sera-Exosome Biomarker of Early Breast Cancer
Ref 2 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.

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