Disease Information
General Information of the Disease (ID: DIS00403)
| Name |
Ischemia/reperfusion injury
|
|---|---|
| ICD |
ICD-11: DB98
|
| Resistance Map |
Type(s) of Resistant Mechanism of This Disease
Drug Resistance Data Categorized by Drug
Approved Drug(s)
2 drug(s) in total
| Drug Resistance Data Categorized by Their Corresponding Mechanisms | ||||
|
|
||||
| Key Molecule: Long non-protein coding RNA (ACART) | [1] | |||
| Resistant Disease | Ischemia/reperfusion injury [ICD-11: DB98.B] | |||
| Molecule Alteration | Down-regulation | Expression |
||
| Resistant Drug | Hydrogen peroxide | |||
| Experimental Note | Discovered Using In-vivo Testing Model | |||
| Cell Pathway Regulation | PPAR-gama/Bcl-2 signaling pathway | Activation | hsa04933 | |
| In Vitro Model | NMVCs | N.A. | . | N.A. |
| In Vivo Model | C57BL/6 mice and neonatal mice model of I/R injury model | Mus musculus | ||
| Experiment for Molecule Alteration |
Knockdown assay; Overexpression assay | |||
| Experiment for Drug Resistance |
MTT assay; TUNEL assay; Lactate dehydrogenase assay | |||
| Mechanism Description | LncRNA ACART protects cardiomyocytes from apoptosis by activating PPAR- gama /Bcl-2 pathway. | |||
| Drug Resistance Data Categorized by Their Corresponding Mechanisms | ||||
|
|
||||
| Key Molecule: TINCR ubiquitin domain containing (TINCR) | [2] | |||
| Resistant Disease | Ischemia/reperfusion injury [ICD-11: DB98.B] | |||
| Molecule Alteration | Up-regulation | Interaction |
||
| Resistant Drug | Morphine | |||
| Experimental Note | Revealed Based on the Cell Line Data | |||
| In Vitro Model | H9C2 cells | Ovary | Cricetulus griseus (Chinese hamster) | CVCL_A0TS |
| In Vivo Model | Rat model of I/R injury | Rattus norvegicus | ||
| Experiment for Molecule Alteration |
RIP experiments assay; RNA pull down assay; qRT-PCR; Western bloting analysis; Knockdown assay; Overexpression assay | |||
| Experiment for Drug Resistance |
CCK8 assay; TUNEL assay; Flow cytometry assay | |||
| Mechanism Description | MpostC-induced upregulation of TINCR protects cardiomyocytes from I/R injury via inhibiting degradation and ubiquitination of FGF1, and subsequently activating PKCepsilon signaling pathway, which provides a novel insight in the mechanism of TINCR and PKCepsilon during MpostC treatment of I/R injury. | |||
References
visits since 2022
If you find any error in data or bug in web service, please kindly report it to Dr. Sun and Dr. Zhang.
