Molecule Information
General Information of the Molecule (ID: Mol05807)
| Name |
hsa-miR-515-1
,Homo sapiens
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| Molecule Type |
Precursor miRNA
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| Sequence |
UCUCAUGCAGUCAUUCUCCAAAAGAAAGCACUUUCUGUUGUCUGAAAGCAGAGUGCCUUC
UUUUGGAGCGUUACUGUUUGAGA Click to Show/Hide
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| 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 Sensitive Data Categorized by Their Corresponding Mechanisms | ||||
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| Disease Class: Malignant glioma [ICD-11: 2A00.02] | [1] | |||
| Sensitive Disease | Malignant glioma [ICD-11: 2A00.02] | |||
| Sensitive Drug | Paclitaxel | |||
| Molecule Alteration | Expression | Up-regulation |
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| Experimental Note | Revealed Based on the Cell Line Data | |||
| In Vitro Model | IGROV1 cells | Ovary | Homo sapiens (Human) | CVCL_1304 |
| MCAS cells | Ovary | Homo sapiens (Human) | CVCL_3020 | |
| OVCA429 cells | Ovary | Homo sapiens (Human) | CVCL_3936 | |
| OVCA432 cells | Ovary | Homo sapiens (Human) | CVCL_3769 | |
| OVCA433 cells | Ovary | Homo sapiens (Human) | CVCL_0475 | |
| PEO1 cells | Ovary | Homo sapiens (Human) | CVCL_2686 | |
| PEO4 cells | Ovary | Homo sapiens (Human) | CVCL_2690 | |
| TOV-112D cells | Ovary | Homo sapiens (Human) | CVCL_3612 | |
| TOV21G cells | Ovary | Homo sapiens (Human) | CVCL_3613 | |
| OVCAR10 cells | Ovary | Homo sapiens (Human) | CVCL_4377 | |
| OVCAR8 cells | Ovary | Homo sapiens (Human) | CVCL_1629 | |
| OVCAR5 cells | Ovary | Homo sapiens (Human) | CVCL_1628 | |
| OVCAR4 cells | Ovary | Homo sapiens (Human) | CVCL_1627 | |
| Experiment for Molecule Alteration |
RT-PCR | |||
| Experiment for Drug Resistance |
MTS assay | |||
| Mechanism Description | Based on miRNA expression and GI50 data, Pearson's correlation test identified 35 miRNAs associated with in vitro paclitaxel sensitivity (P<0.05). | |||
| Drug Resistance Data Categorized by Their Corresponding Mechanisms | ||||
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| Disease Class: Breast cancer [ICD-11: 2C60.2] | [2] | |||
| Resistant Disease | Breast cancer [ICD-11: 2C60.2] | |||
| Resistant Drug | Tamoxifen | |||
| Molecule Alteration | Expression | Up-regulation |
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| Experimental Note | Revealed Based on the Cell Line Data | |||
| Cell Pathway Regulation | PI3K-AKT signalling pathway | Regulation | N.A. | |
| Cell cycle pathways | Regulation | N.A. | ||
| In Vitro Model | MCF-7 cells | Breast | Homo sapiens (Human) | CVCL_0031 |
| Experiment for Molecule Alteration |
qRT-PCR | |||
| Experiment for Drug Resistance |
Cell viability assay; Cell cycle assays; Apoptosis assay | |||
| Mechanism Description | Our findings indicate that tamoxifen-resistant cells express miRNA-519a at high levels, which directly represses the expression of PTEN, RB1, and CDKN1A, central nodes of a dense network, allowing the cells to proliferate, even in the presence of tamoxifen. | |||
| Drug Resistance Data Categorized by Their Corresponding Mechanisms | ||||
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| Disease Class: Ovarian cancer [ICD-11: 2C73.0] | [3] | |||
| Resistant Disease | Ovarian cancer [ICD-11: 2C73.0] | |||
| Resistant Drug | Topotecan | |||
| Molecule Alteration | Expression | . |
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| Experimental Note | Revealed Based on the Cell Line Data | |||
| In Vitro Model | TOV21G cells | Ovary | Homo sapiens (Human) | CVCL_3613 |
| TOV112D cells | Ovary | Homo sapiens (Human) | CVCL_3612 | |
| C13 cells | Ovary | Homo sapiens (Human) | CVCL_0114 | |
| OV2008 cells | Ovary | Homo sapiens (Human) | CVCL_0473 | |
| A2780CP cells | Ovary | Homo sapiens (Human) | CVCL_0135 | |
| A2780s cells | Ovary | Homo sapiens (Human) | CVCL_4863 | |
| IGROV1 cells | Ovary | Homo sapiens (Human) | CVCL_1304 | |
| OVCAR5 cells | Ovary | Homo sapiens (Human) | CVCL_1628 | |
| OVCAR3 cells | Ovary | Homo sapiens (Human) | CVCL_0465 | |
| SkOV3 cells | Ovary | Homo sapiens (Human) | CVCL_0532 | |
| Experiment for Molecule Alteration |
miRNA probe assay | |||
| Experiment for Drug Resistance |
Cell proliferation assays | |||
| Mechanism Description | MicroRNAs (miRNAs) are 19 to 25-nucleotide, non-coding, RNA transcripts, thought to be instrumental in controlling eukaryotic cell function via modulation of post-transcriptional activity of multiple target mRNA genes by repression of translation or regulation of mRNA degradation. | |||
References
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