Evidence map›Paper›PMID 30323297›Full record

ArticleScientific reports2018

Raman micro-spectroscopy monitors acquired resistance to targeted cancer therapy at the cellular level.

Mohamad K Hammoud, Hesham K Yosef, Tatjana Lechtonen, Karim Aljakouch, Martin Schuler, Wissam Alsaidi, Ibrahim Daho, Abdelouahid Maghnouj, Stephan Hahn, Samir F El-Mashtoly and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
4.9field-weighted citation impact, top 5% 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

10 citing papers in PubMed, 36 citations in OpenAlex.

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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

11 authors at 2 institutions in 1 country.

Mohamad K HammoudDepartment of Biophysics, Ruhr-University Bochum, 44780, Bochum, Germany.
Hesham K YosefDepartment of Biophysics, Ruhr-University Bochum, 44780, Bochum, Germany.ORCID http://orcid.org/0000-0002-2385-0046
Tatjana LechtonenDepartment of Biophysics, Ruhr-University Bochum, 44780, Bochum, Germany.
Karim AljakouchDepartment of Biophysics, Ruhr-University Bochum, 44780, Bochum, Germany.
Martin SchulerDepartment of Biophysics, Ruhr-University Bochum, 44780, Bochum, Germany.
Wissam AlsaidiDepartment of Biophysics, Ruhr-University Bochum, 44780, Bochum, Germany.
Ibrahim DahoDepartment of Biophysics, Ruhr-University Bochum, 44780, Bochum, Germany.
Abdelouahid MaghnoujDepartment of Molecular GI-Oncology, Clinical Research Center, Ruhr-University Bochum, 44780, Bochum, Germany.
Stephan HahnDepartment of Molecular GI-Oncology, Clinical Research Center, Ruhr-University Bochum, 44780, Bochum, Germany.
Samir F El-MashtolyDepartment of Biophysics, Ruhr-University Bochum, 44780, Bochum, Germany. samir@bph.rub.de.ORCID http://orcid.org/0000-0001-6087-8817
Klaus GerwertDepartment of Biophysics, Ruhr-University Bochum, 44780, Bochum, Germany.
Ruhr University Bochum · DEUniversity Hospitals of the Ruhr-University of Bochum · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monitoring the drug efficacy or resistance in vitro is usually carried out by measuring the response of single few proteins. However, observation of single proteins instead of an integral cell response may lead to results that are not consistent with patient's response to a drug. We present a Raman spectroscopic method that detects the integral cell response to drugs such as tyrosine kinase inhibitors (TKIs). Non-small cell lung cancer (NSCLC) patients with EGFR mutations develop acquired resistance to first (erlotinib)- and third (osimertinib)-generation TKIs. Large erlotinib-induced differences were detected by Raman micro-spectroscopy in NSCLC cells without T790M EGFR mutation but not in cells with this mutation. Additionally, Raman difference spectra detected the response of NSCLC cells with T790M EGFR mutation to second- (neratinib) and third-generation (osimertinib) TKIs, and the resistance of cells with T790M/C797S EGFR mutation to osimertinib. Thus, the in vitro Raman results indicated that NSCLC cells with T790M and T790M/C797S EGFR mutations are resistant to erlotinib- and osimertinib, respectively, consistent with the observed responses of patients. This study shows the potential of Raman micro-spectroscopy to monitor drug resistance and opens a new door to in vitro companion diagnostics for screening personalized therapies.

Indexed as

Drug Resistance, NeoplasmSpectrum Analysis, RamanAmino Acid SubstitutionCarcinoma, Non-Small-Cell LungDrug MonitoringDrug Screening Assays, AntitumorErbB ReceptorsHumansLung NeoplasmsMolecular Targeted TherapyPrecision MedicineProtein Kinase InhibitorsTreatment OutcomeTumor Cells, CulturedEGFR protein, humanErbB ReceptorsProtein Kinase Inhibitors

Identifiers

PMID30323297
PMCPMC6189084
OpenAlexW2896433658

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.