Evidence map›Paper›PMID 29645336›Full record

ArticleAngewandte Chemie (International ed. in English)2018

Raman Microspectroscopic Evidence for the Metabolism of a Tyrosine Kinase Inhibitor, Neratinib, in Cancer Cells.

Karim Aljakouch, Tatjana Lechtonen, Hesham K Yosef, Mohamad K Hammoud, Wissam Alsaidi, Carsten Kötting, Carolin Mügge, Robert Kourist, Samir F El-Mashtoly, Klaus Gerwert

Open access · hybridAbstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
8.5field-weighted citation impact, top 2% 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

40 citing papers in PubMed, 86 citations in OpenAlex.

  1. Review
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  5. Raman imaging of molecular groups in the wavenumber silent region.Analytical and bioanalytical chemistry · 2026
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  20. Raman Spectroscopy for Chemical Biology Research.Journal of the American Chemical Society · 2022
    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

10 authors at 2 institutions in 2 countries.

Karim AljakouchBiophysics Department, Ruhr-University Bochum, Germany.ORCID 0000-0002-8330-512X
Tatjana LechtonenBiophysics Department, Ruhr-University Bochum, Germany.ORCID 0000-0002-8118-4715
Hesham K YosefBiophysics Department, Ruhr-University Bochum, Germany.ORCID 0000-0002-2385-0046
Mohamad K HammoudBiophysics Department, Ruhr-University Bochum, Germany.ORCID 0000-0002-3019-7794
Wissam AlsaidiBiophysics Department, Ruhr-University Bochum, Germany.ORCID 0000-0002-7863-3196
Carsten KöttingBiophysics Department, Ruhr-University Bochum, Germany.ORCID 0000-0002-3599-9657
Carolin MüggeJunior Research Group for Microbial Biotechnology, Ruhr-University Bochum, Germany.ORCID 0000-0002-8065-173X
Robert KouristInstitute of Molecular Biotechnology, Graz University of Technology, Austria.ORCID 0000-0002-2853-3525
Samir F El-MashtolyBiophysics Department, Ruhr-University Bochum, Germany.ORCID 0000-0001-6087-8817
Klaus GerwertBiophysics Department, Ruhr-University Bochum, Germany.ORCID 0000-0001-8759-5964
Ruhr University Bochum · DEInstitute of Molecular Biotechnology · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tyrosine kinase receptors are one of the main targets in cancer therapy. They play an essential role in the modulation of growth factor signaling and thereby inducing cell proliferation and growth. Tyrosine kinase inhibitors such as neratinib bind to EGFR and HER2 receptors and exhibit antitumor activity. However, little is known about their detailed cellular uptake and metabolism. Here, we report for the first time the intracellular spatial distribution and metabolism of neratinib in different cancer cells using label-free Raman imaging. Two new neratinib metabolites were detected and fluorescence imaging of the same cells indicate that neratinib accumulates in lysosomes. The results also suggest that both EGFR and HER2 follow the classical endosome lysosomal pathway for degradation. A combination of Raman microscopy, DFT calculations, and LC-MS was used to identify the chemical structure of neratinib metabolites. These results show the potential of Raman microscopy to study drug pharmacokinetics.

Indexed as

Cell Line, TumorErb-b2 Receptor Tyrosine KinasesErbB ReceptorsHumansLysosomesNeoplasmsProtein Kinase InhibitorsQuinolinesSpectrum Analysis, RamanERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesErbB ReceptorsneratinibProtein Kinase InhibitorsQuinolinescancerlabel-free imagingmetabolismRaman spectroscopytyrosine kinase inhibitors

Identifiers

PMID29645336
PMCPMC6033014
OpenAlexW2797105107

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.