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Publication

Differential protein stability of EGFR mutants determines responsiveness to tyrosine kinase inhibitors.

Authors not recorded

Oncotarget2016PMID 27612423PMC5356576stubpubmedProvenance
Source
PubMed
Retrieved
Sep 8, 2026
Layer
normalized (units and labels harmonized; values unchanged)
Run
ING-CIVIC-20260908-000001
Published

Abstract

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Linked entities

Linked entities (4)

How each link was made (MeSH, dictionary, registry reference, curation…) and whether it has been validated. Candidate links are not counted in entity statistics.

Validated 4

Curated evidence

Evidence citing this paper (2)

civicProvenance
Source
CIViC — Clinical Interpretation of Variants in Cancer
Dataset
CIViC evidence items
Version
civic-2026-09-08
Retrieved
Sep 8, 2026
Layer
normalized (units and labels harmonized; values unchanged)
Evidence
expert curation
License
CC0 1.0
PMID
27612423
Run
ING-CIVIC-20260908-000001
Open at source
CuratedShowing 1–2 of 2 evidence items · levels, directions and significance as curated at the source; each row links to its CIViC record.
TherapyCancerTypeLevelDirection · significanceRating (1–5)StatusEvidenceSource
EGFR E746_A750del1
ErlotinibLung Non-Small Cell CarcinomaCURATED_BROADERPredictiveDSupports Sensitivity Response—submitted
EID4204

In an in vitro study, HCC827 cells expressing EGFR E746_A750del mutation were associated with sensitivity to erlotinib treatment. Sensitivity was determined by assessing cell density and ERK phosphory… (full text at CIViC)

PMID 27612423 · Ray et al., 2016 · Open in CIViC

civic
EGFR L858R1
ErlotinibLung Non-Small Cell CarcinomaCURATED_BROADERPredictiveDSupports Sensitivity Response1accepted
EID4287

In an in vitro study, CHO and NCI-H3255 cells expressing EGFR L858R mutation were associated with sensitivity to erlotinib treatment. Sensitivity was determined by assessing cell density.

PMID 27612423 · Ray et al., 2016 · Open in CIViC

civic