Drug (ID: DG00631) and It's Reported Resistant Information
Name
Clozatinib
Drug Resistance Disease(s)
Disease(s) with Resistance Information Discovered by Cell Line Test for This Drug (1 diseases)
Diffuse large B-cell lymphoma [ICD-11: 2A81]
[1]
Target . NOUNIPROTAC [1]
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
Click to Show/Hide the Resistance Disease of This Class
Diffuse large B-cell lymphoma [ICD-11: 2A81]
Click to Show/Hide
Drug Resistance Data Categorized by Their Corresponding Mechanisms
       Epigenetic Alteration of DNA, RNA or Protein (EADR) Click to Show/Hide
Key Molecule: Zinc finger C3HC-type containing 1 (ZC3HC1) [1]
Molecule Alteration Expression
Up-regulation
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
Ref 1 Treatment Efficacy and Resistance Mechanisms Using the Second-Generation ALK Inhibitor AP26113 in Human NPM-ALK-Positive Anaplastic Large Cell Lymphoma .Mol Cancer Res. 2015 Apr;13(4):775-83. doi: 10.1158/1541-7786.MCR-14-0157. Epub 2014 Nov 24. 10.1158/1541-7786.MCR-14-0157

If you find any error in data or bug in web service, please kindly report it to Dr. Sun and Dr. Zhang.