Drug Information
Drug (ID: DG01904) and It's Reported Resistant Information
| Name |
EAP Protocol
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| Synonyms |
EAP Protocol
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Type(s) of Resistant Mechanism of This Drug
Drug Resistance Data Categorized by Their Corresponding Diseases
ICD-02: Benign/in-situ/malignant neoplasm
| Drug Sensitivity Data Categorized by Their Corresponding Mechanisms | |||||||||||||
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| Key Molecule: Cellular tumor antigen p53 (TP53) | [1] | ||||||||||||
| Sensitive Disease | Gastric adenocarcinoma [ICD-11: 2B72.0] | ||||||||||||
| Molecule Alteration | Missense mutation | p.R175H (c.524G>A) |
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| Wild Type Structure | Method: X-ray diffraction | Resolution: 2.37 Å | |||||||||||
| Mutant Type Structure | Method: X-ray diffraction | Resolution: 2.38 Å | |||||||||||
| Download The Information of Sequence | Download The Structure File | ||||||||||||
-
H
H
M
M
170
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T
T
E
E
V
V
V
V
R
R
R
H
C
C
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| Experimental Note | Identified from the Human Clinical Data | ||||||||||||
| In Vitro Model | Stomach | N.A. | |||||||||||
| Experiment for Molecule Alteration |
Immunoblotting analysis | ||||||||||||
| Mechanism Description | The missense mutation p.R175H (c.524G>A) in gene TP53 cause the sensitivity of EAP Protocol by unusual activation of pro-survival pathway | ||||||||||||
| Key Molecule: Cellular tumor antigen p53 (TP53) | [1] | ||||||||||||
| Sensitive Disease | Gastric adenocarcinoma [ICD-11: 2B72.0] | ||||||||||||
| Molecule Alteration | Missense mutation | p.R282L (c.845G>T) |
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| Experimental Note | Identified from the Human Clinical Data | ||||||||||||
| In Vitro Model | Stomach | N.A. | |||||||||||
| Experiment for Molecule Alteration |
Immunoblotting analysis | ||||||||||||
| Mechanism Description | The missense mutation p.R282L (c.845G>T) in gene TP53 cause the sensitivity of EAP Protocol by unusual activation of pro-survival pathway | ||||||||||||
| Key Molecule: Cellular tumor antigen p53 (TP53) | [1] | ||||||||||||
| Sensitive Disease | Gastric adenocarcinoma [ICD-11: 2B72.0] | ||||||||||||
| Molecule Alteration | Missense mutation | p.R213P (c.638G>C) |
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| Experimental Note | Identified from the Human Clinical Data | ||||||||||||
| In Vitro Model | Stomach | N.A. | |||||||||||
| Experiment for Molecule Alteration |
Immunoblotting analysis | ||||||||||||
| Mechanism Description | The missense mutation p.R213P (c.638G>C) in gene TP53 cause the sensitivity of EAP Protocol by unusual activation of pro-survival pathway | ||||||||||||
References
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