Molecule Information
General Information of the Molecule (ID: Mol01711)
| Name |
hsa-miR-193a-5p
,Homo sapiens
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| Synonyms |
microRNA 193a
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| Molecule Type |
Mature miRNA
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| Sequence |
UGGGUCUUUGCGGGCGAGAUGA
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| Ensembl ID | |||||
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| Mature Accession | |||||
| Click to Show/Hide the Complete Species Lineage | |||||
Type(s) of Resistant Mechanism of This Molecule
Drug Resistance Data Categorized by Drug
Approved Drug(s)
3 drug(s) in total
| Drug Resistance Data Categorized by Their Corresponding Mechanisms | ||||
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| Disease Class: Testicular cancer [.] | [1] | |||
| Resistant Disease | Testicular cancer [.] | |||
| Resistant Drug | Cisplatin | |||
| Molecule Alteration | Expression | Down-regulation |
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| Experimental Note | Revealed Based on the Cell Line Data | |||
| Experiment for Molecule Alteration |
RT-qPCR with "Low Density Array" | |||
| Experiment for Drug Resistance |
MTT assay | |||
| Mechanism Description | Examining almost all known human micro-RNA species confirmed the miR-371-373 cluster as a promising target for explaining cisplatin resistance, potentially by counteracting wild-type P53 induced senescence or linking it with the potency to differentiate. Moreover, we describe for the first time an association of the up-regulation of micro-RNA species such as hsa-miR-512-3p/-515/-517/-518/-525 and down-regulation of hsa-miR-99a/-100/-145 with a cisplatin resistant phenotype in human germ cell tumors. | |||
| Drug Sensitivity Data Categorized by Their Corresponding Mechanisms | ||||
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| Disease Class: Prostate cancer [ICD-11: 2C82.0] | [2] | |||
| Sensitive Disease | Prostate cancer [ICD-11: 2C82.0] | |||
| Sensitive Drug | Docetaxel | |||
| Molecule Alteration | Expression | Down-regulation |
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| Experimental Note | Identified from the Human Clinical Data | |||
| Cell Pathway Regulation | miR193a-5p/Bach2/HO1 signaling pathway | Inhibition | hsa05206 | |
| In Vitro Model | DU-145 cells | Prostate | Homo sapiens (Human) | CVCL_0105 |
| LNCaP cells | Prostate | Homo sapiens (Human) | CVCL_0395 | |
| PC3 cells | Prostate | Homo sapiens (Human) | CVCL_0035 | |
| T24 cells | Bladder | Homo sapiens (Human) | CVCL_0554 | |
| RWPE-1 cells | Prostate | Homo sapiens (Human) | CVCL_3791 | |
| UM-UC-3 cells | Bladder | Homo sapiens (Human) | CVCL_1783 | |
| In Vivo Model | Nude mouse xenograft model | Mus musculus | ||
| Experiment for Molecule Alteration |
qRT-PCR | |||
| Experiment for Drug Resistance |
TUNEL assays | |||
| Mechanism Description | Silencing of miR193a-5p or blockade of the miR193a-5p-Bach2-HO-1 pathway enhances sensitization of PC3 cells to docetaxel-induced apoptosis. Docetaxel-induced miR193a-5p upregulation, which in turn inhibits Bach2 expression and thus relieves Bach2 repression of HO-1 expression, partly counteracted docetaxel-induced apoptosis. | |||
| Drug Sensitivity Data Categorized by Their Corresponding Mechanisms | ||||
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| Disease Class: Glioma [ICD-11: 2A00.1] | [3] | |||
| Sensitive Disease | Glioma [ICD-11: 2A00.1] | |||
| Sensitive Drug | Temozolomide | |||
| Molecule Alteration | Expression | Down-regulation |
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| Experimental Note | Identified from the Human Clinical Data | |||
| In Vitro Model | U87 cells | Brain | Homo sapiens (Human) | CVCL_0022 |
| U257 cells | Brain | Homo sapiens (Human) | N.A. | |
| Experiment for Molecule Alteration |
qPCR | |||
| Experiment for Drug Resistance |
Flow cytometry assay; MTT assay; Transwell assay | |||
| Mechanism Description | Upregulation of CASC2 sensitized glioma to temozolomide cytotoxicity through autophagy inhibition by sponging miR193a-5p and regulating mTOR expression. mTOR or CASC2 overexpression or miR193a-5p inhibition remarkably reduced autophagy-related proteins expression. | |||
References
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