Disease Information
General Information of the Disease (ID: DIS00547)
| Name |
Ovarian cancer
|
|---|---|
| ICD |
ICD-11: 2C73
|
| 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 | ||||
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| Key Molecule: Cystine/glutamate transporter (SLC7A11) | [1] | |||
| Metabolic Type | Redox metabolism | |||
| Resistant Disease | Ovarian clear cell carcinoma [ICD-11: 2C73.00] | |||
| Resistant Drug | Docetaxel | |||
| Molecule Alteration | Expression | Up-regulation |
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| Differential expression of the molecule in resistant disease | ||||
| Classification of Disease | Ovarian cancer [ICD-11: 2C73] | |||
| The Specified Disease | Ovarian cancer | |||
| The Studied Tissue | Ovarian tissue | |||
| The Expression Level of Disease Section Compare with the Healthy Individual Tissue | p-value: 2.27E-01 Fold-change: 1.23E-01 Z-score: 1.31E+00 |
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| Experimental Note | Revealed Based on the Cell Line Data | |||
| In Vitro Model | Caov-3 cells | Ovary | Homo sapiens (Human) | CVCL_0201 |
| ES-2 cells | Ovary | Homo sapiens (Human) | CVCL_3509 | |
| HAC-2 cells | Ovary | Homo sapiens (Human) | CVCL_8354 | |
| RMG-1 cells | Ascites | Homo sapiens (Human) | CVCL_1662 | |
| SKOV-3 cells | Ovary | Homo sapiens (Human) | CVCL_0532 | |
| TOV21G cells | Ovary | Homo sapiens (Human) | CVCL_3613 | |
| Experiment for Molecule Alteration |
Western blot analysis | |||
| Experiment for Drug Resistance |
IC50 assay | |||
| Mechanism Description | This study demonstrated that combined treatment with paclitaxel (PTX) and the xCT inhibitor sulfasalazine (SAS) significantly enhanced cytotoxicity more than the individual drugs did in OCCC cells. Treatment with PTX and SAS induced apoptosis more effectively than did individual drug treatments in the cells with significant generation of ROS. | |||
| Drug Sensitivity Data Categorized by Their Corresponding Mechanisms | ||||
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| Key Molecule: Cystine/glutamate transporter (SLC7A11) | [1] | |||
| Metabolic Type | Redox metabolism | |||
| Sensitive Disease | Ovarian clear cell carcinoma [ICD-11: 2C73.00] | |||
| Sensitive Drug | Sulfasalazine | |||
| Molecule Alteration | Expression | Up-regulation |
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| Experimental Note | Revealed Based on the Cell Line Data | |||
| In Vitro Model | Caov-3 cells | Ovary | Homo sapiens (Human) | CVCL_0201 |
| ES-2 cells | Ovary | Homo sapiens (Human) | CVCL_3509 | |
| HAC-2 cells | Ovary | Homo sapiens (Human) | CVCL_8354 | |
| RMG-1 cells | Ascites | Homo sapiens (Human) | CVCL_1662 | |
| SKOV-3 cells | Ovary | Homo sapiens (Human) | CVCL_0532 | |
| TOV21G cells | Ovary | Homo sapiens (Human) | CVCL_3613 | |
| Experiment for Molecule Alteration |
Western blot analysis | |||
| Experiment for Drug Resistance |
IC50 assay | |||
| Mechanism Description | This study demonstrated that combined treatment with paclitaxel (PTX) and the xCT inhibitor sulfasalazine (SAS) significantly enhanced cytotoxicity more than the individual drugs did in OCCC cells. Treatment with PTX and SAS induced apoptosis more effectively than did individual drug treatments in the cells with significant generation of ROS. | |||
References
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