Evidence map›Paper›PMID 28974758›Full record

ArticleScientific reports2017

Evaluation of the heterogeneous tissue distribution of erlotinib in lung cancer using matrix-assisted laser desorption ionization mass spectrometry imaging.

Yukari Tsubata, Mitsuhiro Hayashi, Ryosuke Tanino, Hiroaki Aikawa, Mayu Ohuchi, Kenji Tamura, Yasuhiro Fujiwara, Takeshi Isobe, Akinobu Hamada

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. 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
1.4field-weighted citation impact, top 16% 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, 29 citations in OpenAlex.

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  10. Restriction of drug transport by the tumor environment.Histochemistry and cell biology · 2018
    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 at 2 institutions in 3 countries.

Yukari TsubataDivision of Medical Oncology and Respiratory Medicine, Department of Internal Medicine, Shimane University, School of Medicine, 89-1 Enya-cho, Izumo, Shimane, 693-8501, Japan.ORCID 0000-0002-4260-2849
Mitsuhiro HayashiDivision of Molecular Pharmacology, National Cancer Center Research Institute, National Cancer Center, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045, Japan.
Ryosuke TaninoDivision of Medical Oncology and Respiratory Medicine, Department of Internal Medicine, Shimane University, School of Medicine, 89-1 Enya-cho, Izumo, Shimane, 693-8501, Japan.ORCID 0000-0002-5148-9526
Hiroaki AikawaDivision of Clinical Pharmacology and Translational Research, Exploratory Oncology Research and Clinical Trial Center, National Cancer Center, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045, Japan.
Mayu OhuchiDivision of Molecular Pharmacology, National Cancer Center Research Institute, National Cancer Center, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045, Japan.
Kenji TamuraDepartment of Breast and Medical Oncology, National Cancer Center Hospital, National Cancer Center, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045, Japan.
Yasuhiro FujiwaraDepartment of Breast and Medical Oncology, National Cancer Center Hospital, National Cancer Center, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045, Japan.
Takeshi IsobeDivision of Medical Oncology and Respiratory Medicine, Department of Internal Medicine, Shimane University, School of Medicine, 89-1 Enya-cho, Izumo, Shimane, 693-8501, Japan.
Akinobu HamadaDivision of Molecular Pharmacology, National Cancer Center Research Institute, National Cancer Center, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045, Japan. akhamad@ncc.go.jp.
Shimane University · JPNational Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although drug distribution in tumor tissues has a significant impact on efficacy, conventional pharmacokinetic analysis has some limitations with regard to its ability to provide a comprehensive assessment of drug tissue distribution. Erlotinib is a tyrosine kinase inhibitor that acts on the epidermal growth factor receptor; however, it is unclear how this drug is histologically distributed in lung cancer. We used matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-MSI) and liquid chromatography-tandem mass spectrometry (LC-MS/MS) to analyze erlotinib distribution in the tumor and normal lung tissues of a mouse xenograft model and patient with non-small cell lung cancer. LC-MS/MS showed that the erlotinib tissue concentration in the xenograft tumor tissue was clearly lower than that in the normal tissue at the time of maximum blood concentration. MALDI-MSI showed the heterogeneous distribution of erlotinib at various levels in the murine tissues; interestingly, erlotinib was predominantly localized in the area of viable tumor compared to the necrotic area. In the patient-derived tissue, MALDI-MSI showed that there were different concentrations of erlotinib distributed within the same tissue. For drug development and translational research, the imaging pharmacokinetic study used the combination of MALDI-MSI and LC-MS/MS analyses may be useful in tissues with heterogeneous drug distribution.

Indexed as

AnimalsErlotinib HydrochlorideHumansLungLung NeoplasmsMiceProtein Kinase InhibitorsSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationTissue DistributionXenograft Model Antitumor AssaysErlotinib HydrochlorideProtein Kinase Inhibitors

Identifiers

PMID28974758
PMCPMC5626687
OpenAlexW2758766875

What OpenQuestion holds

Textmetadata
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.