Drug Information
Drug (ID: DG00631) and It's Reported Resistant Information
Type(s) of Resistant Mechanism of This Drug
EADR: Epigenetic Alteration of DNA, RNA or Protein
Drug Resistance Data Categorized by Their Corresponding Diseases
ICD-02: Benign/in-situ/malignant neoplasm
Diffuse large B-cell lymphoma [ICD-11: 2A81]
Drug Resistance Data Categorized by Their Corresponding Mechanisms | ||||
Epigenetic Alteration of DNA, RNA or Protein (EADR) | ||||
Key Molecule: Zinc finger C3HC-type containing 1 (ZC3HC1) | [1] | |||
Molecule Alteration | Expression | Up-regulation |
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Resistant Disease | NPM-ALK-Positive anaplastic large cell lymphoma [ICD-11: 2A81.8] | |||
Experimental Note | Revealed Based on the Cell Line Data | |||
In Vitro Model | SUP-M2 cells | Colon | Homo sapiens (Human) | CVCL_2209 |
KARPAS-299 cells | Peripheral blood | Homo sapiens (Human) | CVCL_1324 | |
Experiment for Molecule Alteration |
Western blotting analysis | |||
Experiment for Drug Resistance |
Proliferation assay | |||
Mechanism Description | For KARPAS-299-derived cell lines, we observed oncogene overexpression as the main resistance mechanism, whereas in SUP-M2-derived cell lines, we identified several point mutations located within the NPM-ALK kinase domain, which could explain drug resistance. | |||
Key Molecule: Zinc finger C3HC-type containing 1 (ZC3HC1) | [1] | |||
Molecule Alteration | Mutation | p.L1122V+p.139S+p.L1196M+p.S1206C+p.L1122V+p.L1196M+p.L1196M+p.D1203N |
||
Resistant Disease | NPM-ALK-Positive anaplastic large cell lymphoma [ICD-11: 2A81.8] | |||
Experimental Note | Revealed Based on the Cell Line Data | |||
In Vitro Model | SUP-M2 cells | Colon | Homo sapiens (Human) | CVCL_2209 |
KARPAS-299 cells | Peripheral blood | Homo sapiens (Human) | CVCL_1324 | |
Experiment for Molecule Alteration |
Western blotting analysis | |||
Experiment for Drug Resistance |
Proliferation assay | |||
Mechanism Description | For KARPAS-299-derived cell lines, we observed oncogene overexpression as the main resistance mechanism, whereas in SUP-M2-derived cell lines, we identified several point mutations located within the NPM-ALK kinase domain, which could explain drug resistance. |
References
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