Evidence map›Paper›PMID 40194950›Full record

ReviewArchiv der Pharmazie2025

A Structural Insight Into Two Important ErbB Receptors (EGFR and HER2) and Their Relevance to Non-Small Cell Lung Cancer.

Edanur Topalan, Ahmet Büyükgüngör, Melih Çiğdem, Sinan Güra, Belgin Sever, Masami Otsuka, Mikako Fujita, Hasan Demirci, Halilibrahim Ciftci

Abstract readReview
In one paragraph

Review in Archiv der Pharmazie, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Review
  2. HER2 Therapies in Non-Small Cell Lung Cancer (NSCLC).International journal of molecular sciences · 2026
    Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
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

9 authors.

Edanur TopalanDepartment of Molecular Biology and Genetics, Koc University, Istanbul, Türkiye.
Ahmet BüyükgüngörDepartment of Molecular Biology and Genetics, Koc University, Istanbul, Türkiye.ORCID http://orcid.org/0009-0008-0907-1960
Melih ÇiğdemDepartment of Molecular Biology and Genetics, Koc University, Istanbul, Türkiye.ORCID http://orcid.org/0009-0006-8967-4643
Sinan GüraDepartment of Molecular Biology and Genetics, Koc University, Istanbul, Türkiye.
Belgin SeverDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, Anadolu University, Eskisehir, Türkiye.ORCID http://orcid.org/0000-0003-4847-9711
Masami OtsukaMedicinal and Biological Chemistry Science Farm Joint Research Laboratory, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Mikako FujitaMedicinal and Biological Chemistry Science Farm Joint Research Laboratory, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Hasan DemirciDepartment of Molecular Biology and Genetics, Koc University, Istanbul, Türkiye.
Halilibrahim CiftciMedicinal and Biological Chemistry Science Farm Joint Research Laboratory, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.ORCID http://orcid.org/0000-0002-9796-7669

Funding

This study was supported by Scientific and Technological Research Council of Turkey (TUBITAK) under the Grant Number 122Z775 and Health Institutes of Türkiye (TUSEB) under the Grant Number 32988. The authors thank to TUBITAK and TUSEB for their supports. Co-funded by the European Union.
6 · The paper itself

Abstract

The epidermal growth factor receptor (EGFR) family, comprising receptor tyrosine kinases (RTK) such as EGFR and HER2, plays a critical role in various signaling pathways related to cell proliferation, differentiation, and growth. EGFR overactivation due to aberrant signaling can lead to various cancers, including non-small cell lung cancer (NSCLC). To develop treatment for EGFR-related NSCLC, several tyrosine kinase inhibitors (TKIs) were designed: gefitinib, erlotinib, as first-generation; neratinib, dacomitinib as second-generation; osimertinib, lazertinib as third-generation, as examples. However, due to the acquired resistance by the mutations such as EGFR

Indexed as

Antineoplastic AgentsCarcinoma, Non-Small-Cell LungErb-b2 Receptor Tyrosine KinasesLung NeoplasmsProtein Kinase InhibitorsAnimalsErbB ReceptorsHumansMolecular StructureStructure-Activity RelationshipAntineoplastic AgentsEGFR protein, humanERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesErbB ReceptorsProtein Kinase Inhibitorsepidermal growth factor receptor (EGFR)HER2non‐small cell lung cancer (NSCLC)protein structuretyrosine kinase domain mutationstyrosine kinase domain (TKD)tyrosine kinase inhibitors (TKIs)

Identifiers

PMID40194950
PMCPMC11975551

What OpenQuestion holds

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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.