General Information of the Disease (ID: DIS00098)
Name
Ureteral cancer
ICD
ICD-11: 2C92
Type(s) of Resistant Mechanism of This Disease
  ADTT: Aberration of the Drug's Therapeutic Target
  EADR: Epigenetic Alteration of DNA, RNA or Protein
  UAPP: Unusual Activation of Pro-survival Pathway
Drug Resistance Data Categorized by Drug
Approved Drug(s)
2 drug(s) in total
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Cisplatin
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Drug Sensitivity Data Categorized by Their Corresponding Mechanisms
       Epigenetic Alteration of DNA, RNA or Protein (EADR) Click to Show/Hide
Key Molecule: hsa-mir-193b [1]
Sensitive Disease Urothelial carcinoma [ICD-11: 2C92.0]
Molecule Alteration Expression
Up-regulation
Sensitive Drug Cisplatin
Experimental Note Revealed Based on the Cell Line Data
In Vitro Model NTUB1 cells Bladder Homo sapiens (Human) CVCL_RW29
Experiment for
Molecule Alteration
qRT-PCR
Experiment for
Drug Resistance
MTT assay; Flow cytometer
Mechanism Description miR193b Mediates CEBPD-Induced Cisplatin Sensitization Through Targeting ETS1 and Cyclin D1 in Human Urothelial Carcinoma Cells. miR193b-3p, a known tumor suppressor, down-regulated proto-oncogenes Cyclin D1, and ETS1 expression and led to cell cycle arrest, cell invasion, and migration inhibition.
       Unusual Activation of Pro-survival Pathway (UAPP) Click to Show/Hide
Key Molecule: G1/S-specific cyclin-D1 (CCND1) [1]
Sensitive Disease Urothelial carcinoma [ICD-11: 2C92.0]
Molecule Alteration Expression
Down-regulation
Sensitive Drug Cisplatin
Experimental Note Revealed Based on the Cell Line Data
In Vitro Model NTUB1 cells Bladder Homo sapiens (Human) CVCL_RW29
Experiment for
Molecule Alteration
Western blot analysis
Experiment for
Drug Resistance
MTT assay; Flow cytometer
Mechanism Description miR193b Mediates CEBPD-Induced Cisplatin Sensitization Through Targeting ETS1 and Cyclin D1 in Human Urothelial Carcinoma Cells. miR193b-3p, a known tumor suppressor, down-regulated proto-oncogenes Cyclin D1, and ETS1 expression and led to cell cycle arrest, cell invasion, and migration inhibition.
Key Molecule: Protein C-ets-1 (ETS1) [1]
Sensitive Disease Urothelial carcinoma [ICD-11: 2C92.0]
Molecule Alteration Expression
Down-regulation
Sensitive Drug Cisplatin
Experimental Note Revealed Based on the Cell Line Data
In Vitro Model NTUB1 cells Bladder Homo sapiens (Human) CVCL_RW29
Experiment for
Molecule Alteration
Western blot analysis
Experiment for
Drug Resistance
MTT assay; Flow cytometer
Mechanism Description miR193b Mediates CEBPD-Induced Cisplatin Sensitization Through Targeting ETS1 and Cyclin D1 in Human Urothelial Carcinoma Cells. miR193b-3p, a known tumor suppressor, down-regulated proto-oncogenes Cyclin D1, and ETS1 expression and led to cell cycle arrest, cell invasion, and migration inhibition.
Enfortumab
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Drug Sensitivity Data Categorized by Their Corresponding Mechanisms
       Aberration of the Drug's Therapeutic Target (ADTT) Click to Show/Hide
Key Molecule: Nectin cell adhesion molecule 4 (NECTIN4) [2]
Sensitive Disease Advanced urothelial carcinoma [ICD-11: 2C92.Y]
Molecule Alteration Function
Inhibition
Sensitive Drug Enfortumab
Experimental Note Identified from the Human Clinical Data
Cell Pathway Regulation Cell growth Inhibition hsa05200
Cell proliferation Inhibition hsa05200
Cell apoptosis Activation hsa04210
Experiment for
Drug Resistance
Overall survival analysis; Progression-Free Survival analysis
Mechanism Description Nectin-4 is a cell adhesion molecule highly expressed in urothelial carcinoma that may contribute to tumor cell growth and proliferation.Enfortumab vedotin, an antibody-drug conjugate directed against Nectin-4, is comprised of a fully human monoclonal antibody specific for Nectin-4 and monomethyl auristatin E, a microtubule-disrupting agent.
References
Ref 1 MiR-193b Mediates CEBPD-Induced Cisplatin Sensitization Through Targeting ETS1 and Cyclin D1 in Human Urothelial Carcinoma Cells. J Cell Biochem. 2017 Jun;118(6):1563-1573. doi: 10.1002/jcb.25818. Epub 2016 Dec 20.
Ref 2 Enfortumab Vedotin in Previously Treated Advanced Urothelial Carcinoma .N Engl J Med. 2021 Mar 25;384(12):1125-1135. doi: 10.1056/NEJMoa2035807. Epub 2021 Feb 12. 10.1056/NEJMoa2035807

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