Evidence map›Paper›PMID 37557179›Full record

ArticleCell reports. Medicine2023

L858R emerges as a potential biomarker predicting response of lung cancer models to anti-EGFR antibodies: Comparison of osimertinib vs. cetuximab.

Ilaria Marrocco, Suvendu Giri, Arturo Simoni-Nieves, Nitin Gupta, Anna Rudnitsky, Yuya Haga, Donatella Romaniello, Arunachalam Sekar, Mirie Zerbib, Roni Oren and 6 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports. Medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.9field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Translational lung cancer research · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 4 institutions in 3 countries.

Ilaria MarroccoDepartment of Immunology and Regenerative Biology, Weizmann Institute of Science, Rehovot 76100, Israel; Department of Life Sciences and Public Health, Università Cattolica del Sacro Cuore, 00168 Rome, Italy.
Suvendu GiriDepartment of Immunology and Regenerative Biology, Weizmann Institute of Science, Rehovot 76100, Israel.
Arturo Simoni-NievesDepartment of Immunology and Regenerative Biology, Weizmann Institute of Science, Rehovot 76100, Israel.
Nitin GuptaDepartment of Immunology and Regenerative Biology, Weizmann Institute of Science, Rehovot 76100, Israel.
Anna RudnitskyDepartment of Immunology and Regenerative Biology, Weizmann Institute of Science, Rehovot 76100, Israel.
Yuya HagaGraduate School of Pharmaceutical Sciences, Osaka University, Osaka 565-0871, Japan.
Donatella RomanielloDepartment of Medical and Surgical Sciences (DIMEC), University of Bologna, 40126 Bologna, Italy.
Arunachalam SekarDepartment of Immunology and Regenerative Biology, Weizmann Institute of Science, Rehovot 76100, Israel.
Mirie ZerbibDepartment of Veterinary Resources, Weizmann Institute of Science, Rehovot 76100, Israel.
Roni OrenDepartment of Veterinary Resources, Weizmann Institute of Science, Rehovot 76100, Israel.
Moshit LindzenDepartment of Immunology and Regenerative Biology, Weizmann Institute of Science, Rehovot 76100, Israel.
Damon FardDepartment of Life Sciences and Public Health, Università Cattolica del Sacro Cuore, 00168 Rome, Italy.
Yasuo TsutsumiGraduate School of Pharmaceutical Sciences, Osaka University, Osaka 565-0871, Japan; Global Center for Medical Engineering and Informatics, Osaka University, Osaka 565-0871, Japan; Institute for Open and Transdisciplinary Research Initiatives, Osaka University, Osaka 565-0871, Japan.
Mattia LauriolaDepartment of Medical and Surgical Sciences (DIMEC), University of Bologna, 40126 Bologna, Italy.
Luca TamagnoneDepartment of Life Sciences and Public Health, Università Cattolica del Sacro Cuore, 00168 Rome, Italy; Fondazione Policlinico Gemelli - IRCCS, 00168 Rome, Italy.
Yosef YardenDepartment of Immunology and Regenerative Biology, Weizmann Institute of Science, Rehovot 76100, Israel. Electronic address: yosef.yarden@weizmann.ac.il.
Weizmann Institute of Science · ILUniversità Cattolica del Sacro Cuore · ITOsaka University of Pharmaceutical Sciences · JPUniversity of Bologna · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

EGFR-specific tyrosine kinase inhibitors (TKIs), especially osimertinib, have changed lung cancer therapy, but secondary mutations confer drug resistance. Because other EGFR mutations promote dimerization-independent active conformations but L858R strictly depends on receptor dimerization, we herein evaluate the therapeutic potential of dimerization-inhibitory monoclonal antibodies (mAbs), including cetuximab. This mAb reduces viability of cells expressing L858R-EGFR and blocks the FOXM1-aurora survival pathway, but other mutants show no responses. Unlike TKI-treated patient-derived xenografts, which relapse post osimertinib treatment, cetuximab completely prevents relapses of L858R

Indexed as

ErbB ReceptorsLung NeoplasmsAcrylamidesAniline CompoundsAntibodies, MonoclonalBiomarkersCetuximabDNA-Binding ProteinsHumansIndolesNeoplasm Recurrence, LocalProtein Kinase InhibitorsPyrimidinesUbiquitin-Protein LigasesAcrylamidesAniline CompoundsAntibodies, MonoclonalBiomarkersCetuximabDNA-Binding ProteinsErbB ReceptorsIndolesosimertinibProtein Kinase InhibitorsPyrimidinesRAD18 protein, humanUbiquitin-Protein Ligasesadaptive mutabilitycetuximabEGFRkinase inhibitorslung cancermonoclonal antibodyNSCLCosimertinibreceptor tyrosine kinases

Identifiers

PMID37557179
PMCPMC10439256
OpenAlexW4385658197

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.