Drug (ID: DG01867) and It's Reported Resistant Information
Name
ERK inhibitors
Synonyms
ERK inhibitors
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Target . NOUNIPROTAC [1]
Type(s) of Resistant Mechanism of This Drug
  UAPP: Unusual Activation of Pro-survival Pathway
Drug Resistance Data Categorized by Their Corresponding Diseases
ICD-02: Benign/in-situ/malignant neoplasm
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Solid tumour/cancer [ICD-11: 2A00-2F9Z]
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Drug Sensitivity Data Categorized by Their Corresponding Mechanisms
       Unusual Activation of Pro-survival Pathway (UAPP) Click to Show/Hide
Key Molecule: GTPase Nras (NRAS) [2]
Molecule Alteration Missense mutation
p.G12C (c.34G>T)
Sensitive Disease Solid tumour/cancer [ICD-11: 2A00-2F9Z]
Experimental Note Revealed Based on the Cell Line Data
Experiment for
Molecule Alteration
DNA sequencing assay
Experiment for
Drug Resistance
Fluorescence-activated cell sorting assay
Mechanism Description The missense mutation p.G12C (c.34G>T) in gene NRAS cause the sensitivity of ERK inhibitors by unusual activation of pro-survival pathway
Biliary tract cancer [ICD-11: 2C15]
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Drug Sensitivity Data Categorized by Their Corresponding Mechanisms
       Unusual Activation of Pro-survival Pathway (UAPP) Click to Show/Hide
Key Molecule: Serine/threonine-protein kinase B-raf (BRAF) [1]
Molecule Alteration Missense mutation
p.L485W (c.1799T>A)
Sensitive Disease Biliary tract cancer [ICD-11: 2C15.0]
Experimental Note Identified from the Human Clinical Data
Head and neck cancer [ICD-11: 2D42]
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Drug Sensitivity Data Categorized by Their Corresponding Mechanisms
       Unusual Activation of Pro-survival Pathway (UAPP) Click to Show/Hide
Key Molecule: Serine/threonine-protein kinase B-raf (BRAF) [1]
Molecule Alteration Missense mutation
p.G469A (c.1454T>G)
Sensitive Disease Head and neck cancer [ICD-11: 2D42.0]
Experimental Note Identified from the Human Clinical Data
References
Ref 1 Survival outcomes for various treatment modalities in advanced-stage grade 3 follicular lymphoma (FL3): A National Cancer Database (NCDB) study.
Ref 2 Discovery of a novel ERK inhibitor with activity in models of acquired resistance to BRAF and MEK inhibitorsCancer Discov. 2013 Jul;3(7):742-50. doi: 10.1158/2159-8290.CD-13-0070. Epub 2013 Apr 24.

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