Evidence map›Paper›PMID 26617762›Full record

ArticleInternational journal of clinical and experimental pathology2015

Variation in the expression levels of predictive chemotherapy biomarkers in histological subtypes of lung adenocarcinoma: an immunohistochemical study of tissue samples.

Yuichi Fujimoto, Shinsaku Togo, Miniwan Tulafu, Kazue Shimizu, Takuo Hayashi, Toshimasa Uekusa, Yuichirou Honma, Yukiko Namba, Kazuya Takamochi, Shiaki Oh and 2 more

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 75% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
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

12 authors at 2 institutions in 1 country.

Yuichi FujimotoDepartment of Respiratory Medicine, Juntendo University Faculty of Medicine & Graduate School of Medicine 2-1-1 Hongo, Bunkyo-Ku, Tokyo 113-8421, Japan ; Research Institute for Diseases of Old Ages, Juntendo University Graduate School of Medicine 2-1-1 Hongo, Bunkyo-Ku, Tokyo 113-8421, Japan.
Shinsaku TogoDepartment of Respiratory Medicine, Juntendo University Faculty of Medicine & Graduate School of Medicine 2-1-1 Hongo, Bunkyo-Ku, Tokyo 113-8421, Japan ; Research Institute for Diseases of Old Ages, Juntendo University Graduate School of Medicine 2-1-1 Hongo, Bunkyo-Ku, Tokyo 113-8421, Japan.
Miniwan TulafuDepartment of Respiratory Medicine, Juntendo University Faculty of Medicine & Graduate School of Medicine 2-1-1 Hongo, Bunkyo-Ku, Tokyo 113-8421, Japan ; Research Institute for Diseases of Old Ages, Juntendo University Graduate School of Medicine 2-1-1 Hongo, Bunkyo-Ku, Tokyo 113-8421, Japan.
Kazue ShimizuDepartment of Respiratory Medicine, Juntendo University Faculty of Medicine & Graduate School of Medicine 2-1-1 Hongo, Bunkyo-Ku, Tokyo 113-8421, Japan ; Research Institute for Diseases of Old Ages, Juntendo University Graduate School of Medicine 2-1-1 Hongo, Bunkyo-Ku, Tokyo 113-8421, Japan.
Takuo HayashiDepartment of Pathology, Juntendo University School of Medicine 2-1-1 Hongo, Bunkyo-Ku, Tokyo 113-8421, Japan.
Toshimasa UekusaDepartment of Pathology, Labor Health and Welfare Organization Kanto Rosai Hospital 1-1 Kizukisumiyoshi-cho, Nakahara-Ku, Kawasaki, Kanagawa Prefecture 211-8510, Japan.
Yuichirou HonmaDepartment of Respiratory Medicine, Juntendo University Faculty of Medicine & Graduate School of Medicine 2-1-1 Hongo, Bunkyo-Ku, Tokyo 113-8421, Japan ; Research Institute for Diseases of Old Ages, Juntendo University Graduate School of Medicine 2-1-1 Hongo, Bunkyo-Ku, Tokyo 113-8421, Japan.
Yukiko NambaDepartment of Respiratory Medicine, Juntendo University Faculty of Medicine & Graduate School of Medicine 2-1-1 Hongo, Bunkyo-Ku, Tokyo 113-8421, Japan ; Research Institute for Diseases of Old Ages, Juntendo University Graduate School of Medicine 2-1-1 Hongo, Bunkyo-Ku, Tokyo 113-8421, Japan.
Kazuya TakamochiDepartment of General Thoracic Surgery, Juntendo University School of Medicine 2-1-1 Hongo, Bunkyo-Ku, Tokyo 113-8421, Japan.
Shiaki OhDepartment of General Thoracic Surgery, Juntendo University School of Medicine 2-1-1 Hongo, Bunkyo-Ku, Tokyo 113-8421, Japan.
Kenji SuzukiDepartment of General Thoracic Surgery, Juntendo University School of Medicine 2-1-1 Hongo, Bunkyo-Ku, Tokyo 113-8421, Japan.
Kazuhisa TakahashiDepartment of Respiratory Medicine, Juntendo University Faculty of Medicine & Graduate School of Medicine 2-1-1 Hongo, Bunkyo-Ku, Tokyo 113-8421, Japan ; Research Institute for Diseases of Old Ages, Juntendo University Graduate School of Medicine 2-1-1 Hongo, Bunkyo-Ku, Tokyo 113-8421, Japan.
Juntendo University Hospital · JPJuntendo University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLung adenocarcinoma is often composed of a complex and heterogeneous mixture of histological subtypes. Invasive adenocarcinomas are now classified by their predominant pattern, using the comprehensive histological subtyping of the International Association for the Study of Lung Cancer (IASLC), the American Thoracic Society (ATS), and the European Respiratory Society (ERS) classifications. This study aimed to determine whether the expression levels of predictive chemotherapy biomarkers are associated with the histological subtypes proposed by the IASLC/ATS/ERS classification. MATERIALS AND

methodsWe reviewed data on representative tissue samples from 27 patients who received surgical resection and the expression of excision repair cross complementation group 1 (ERCC1), class III β-tubulin, thymidylate synthase (TS), ribonucleotide reductase M1 (RRM1), and c-Met were examined using immunostaining on tumor tissue slides. We assessed immunohistochemical H-scores, as calculated from the intensity and distribution of intratumor expression, according to the IASLC/ATS/ERS histological subtype.

resultsThe expression levels of predictive chemotherapy biomarkers varied according to histological subtype. The H-scores of TS and class III β-tubulin expression levels were higher in solid-type components than they were in lepidic-type components Tumors with solid predominant histology tended to recur earlier than non-solid predominant tumors. However, none of the H-scores in histologically predominant tissues was significantly associated with staging or overall survival.

conclusionsImmunohistochemical H-scores of the predictive chemotherapy biomarkers were strongly associated with histological subtype. The presence of a solid subtype, which was associated with poor outcomes, might be assessed by measuring these biomarkers in mixed subtype adenocarcinomas.

Indexed as

AdenocarcinomaAdultAgedAntineoplastic AgentsBiomarkers, TumorDrug Resistance, NeoplasmFemaleHumansImmunohistochemistryLung NeoplasmsMaleMiddle AgedRetrospective StudiesTreatment OutcomeAntineoplastic AgentsBiomarkers, TumorClass III β-tubulinc-Metexcision repair cross complementation group 1immunohistochemistryribonucleotide reductase M1Thymidylate synthase

Identifiers

PMID26617762
PMCPMC4637577
OpenAlexW2416661204

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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.