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dc.contributor.authorManickavasagar, T
dc.contributor.authorYuan, W
dc.contributor.authorCarreira, S
dc.contributor.authorGurel, B
dc.contributor.authorMiranda, S
dc.contributor.authorFerreira, A
dc.contributor.authorCrespo, M
dc.contributor.authorRiisnaes, R
dc.contributor.authorBaker, C
dc.contributor.authorO’Brien, M
dc.contributor.authorBhosle, J
dc.contributor.authorPopat, S
dc.contributor.authorBanerji, U
dc.contributor.authorLopez, J
dc.contributor.authorBono, JD
dc.contributor.authorMinchom, A
dc.date.accessioned2021-05-27T09:33:49Z
dc.date.available2021-05-27T09:33:49Z
dc.date.issued2020-08-26
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/4590
dc.identifier.doi10.21203/rs.3.rs-59361/v1
dc.description.abstract<h4>Background: </h4> HER-3 has a role in pathogenesis and development of resistance to targeted therapies in non-small cell lung cancer (NSCLC). MethodsWe analysed tumour samples from 45 patients with adenocarcinoma of the lung. HER-3 and HER-2 expression was identified using immunohistochemistry as well as bioinformatic interrogation of The Cancer Genome Atlas (TGCA). ResultsHER-3 was highly expressed in 42.2% of cases and observed more frequently than HER-2 overexpression. ERBB3 copy number alone did not account for HER-3 overexpression. Bioinformatic analysis of TCGA demonstrated that MEK activity score (a score of downstream pathway activity and surrogate of functional HER-3 signalling) did not correlate with HER-3 ligands. EGFR pathway signalling was predominant with a significantly positive correlation of EGFR and AREG expression with MEK activity score. In the ERBB3 expressed group, ERBB3 RNA expression levels were significantly correlated with MEK activity score. ERBB3 expression level remained highly positively correlated with MEK activity after adjusting for EGFR expression. ConclusionHER-3 expression is common and it is not associated with gene amplification nor is it ligand dependent. HER-3 is an alternative pathway to EGFR activating MEK. HER-3 is a potential therapeutic target in NSCLC by virtue of frequent overexpression and functional downstream signalling.
dc.languageeng
dc.language.isoeng
dc.publisherResearch Square
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0
dc.titleHER-3 Expression and MEK Activation in Non-small Cell Lung Cancer
dc.typeJournal Article
dcterms.dateAccepted2021-02-22
rioxxterms.versionVoR
rioxxterms.versionofrecord10.21203/rs.3.rs-59361/v1
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by-nc-nd/4.0
rioxxterms.typeJournal Article/Review
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Therapeutics
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Therapeutics/Cancer Biomarkers
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Cancer Biomarkers
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Therapeutics
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Therapeutics/Cancer Biomarkers
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Cancer Biomarkers
pubs.embargo.termsNot known
icr.researchteamCancer Biomarkers
icr.researchteamCancer Biomarkers
dc.contributor.icrauthorGurel, Bora
dc.contributor.icrauthorCrespo, Mateus


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Except where otherwise noted, this item's license is described as https://creativecommons.org/licenses/by-nc-nd/4.0