Evidence map›Paper›PMID 25548429›Full record

ArticleDisease markers2014

CLCA2 as a novel immunohistochemical marker for differential diagnosis of squamous cell carcinoma from adenocarcinoma of the lung.

Kazuya Shinmura, Hisaki Igarashi, Hisami Kato, Yuichi Kawanishi, Yusuke Inoue, Satoki Nakamura, Hiroshi Ogawa, Takashi Yamashita, Akikazu Kawase, Kazuhito Funai and 1 more

Open access · hybridAbstract readComparative Study
In one paragraph

Article in Disease markers, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

16 citing papers in PubMed, 28 citations in OpenAlex.

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  6. Polymodal Control of TMEM16x Channels and Scramblases.International journal of molecular sciences · 2022
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  16. The impact of the Cancer Genome Atlas on lung cancer.Translational research : the journal of laboratory and clinical medicine · 2015
    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

11 authors at 2 institutions in 1 country.

Kazuya ShinmuraDepartment of Tumor Pathology, Hamamatsu University School of Medicine, 1-20-1 Handayama, Higashi-ku, Hamamatsu, Shizuoka 431-3192, Japan.ORCID 0000-0003-4963-746X
Hisaki IgarashiDepartment of Tumor Pathology, Hamamatsu University School of Medicine, 1-20-1 Handayama, Higashi-ku, Hamamatsu, Shizuoka 431-3192, Japan.
Hisami KatoDepartment of Tumor Pathology, Hamamatsu University School of Medicine, 1-20-1 Handayama, Higashi-ku, Hamamatsu, Shizuoka 431-3192, Japan.
Yuichi KawanishiResearch Equipment Center, Hamamatsu University School of Medicine, Hamamatsu 431-3192, Japan.
Yusuke InoueDepartment of Tumor Pathology, Hamamatsu University School of Medicine, 1-20-1 Handayama, Higashi-ku, Hamamatsu, Shizuoka 431-3192, Japan ; Department of Internal Medicine 2, Hamamatsu University School of Medicine, Hamamatsu 431-3192, Japan.
Satoki NakamuraDepartment of Tumor Pathology, Hamamatsu University School of Medicine, 1-20-1 Handayama, Higashi-ku, Hamamatsu, Shizuoka 431-3192, Japan.
Hiroshi OgawaDivision of Pathology, Seirei Mikatahara General Hospital, Hamamatsu 433-8558, Japan.
Takashi YamashitaDepartment of Surgery 1, Hamamatsu University School of Medicine, Hamamatsu 431-3192, Japan.
Akikazu KawaseDepartment of Surgery 1, Hamamatsu University School of Medicine, Hamamatsu 431-3192, Japan.
Kazuhito FunaiDepartment of Surgery 1, Hamamatsu University School of Medicine, Hamamatsu 431-3192, Japan.
Haruhiko SugimuraDepartment of Tumor Pathology, Hamamatsu University School of Medicine, 1-20-1 Handayama, Higashi-ku, Hamamatsu, Shizuoka 431-3192, Japan.ORCID 0000-0002-0779-3088
Hamamatsu University School of Medicine · JPSeirei Mikatabara General Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent progress in targeted therapy for lung cancer has revealed that accurate differential diagnosis between squamous cell carcinoma (SCC) and adenocarcinoma (ADC) of the lung is essential. To identify a novel immunohistochemical marker useful for differential diagnosis between the two subtypes of lung cancer, we first selected 24 SCC-specific genes and 6 ADC-specific genes using data (case number, 980) from the Cancer Genome Atlas (TCGA) database. Among the genes, we chose the CLCA2 gene, which is involved in chloride conductance and whose protein expression in lung cancer is yet to be characterized, and evaluated its protein expression status in 396 cases of primary lung cancer at Hamamatsu University Hospital. Immunohistochemical analysis revealed a significantly higher CLCA2 expression level in the SCCs than in the ADCs (P < 0.0001) and also a significantly higher frequency of CLCA2 protein expression in the SCCs (104/161, 64.6%) as compared with that in the ADCs (2/235, 0.9%) (P < 0.0001; sensitivity 64.6%, specificity 99.1%). The CLCA2 protein expression status was associated with the histological tumor grade in the SCCs. These results suggest that CLCA2 might be a novel excellent immunohistochemical marker for differentiating between primary SCC and primary ADC of the lung.

Indexed as

AdenocarcinomaBiomarkers, TumorCarcinoma, Squamous CellChloride ChannelsDiagnosis, DifferentialFemaleGene ExpressionHumansKaplan-Meier EstimateLungLung NeoplasmsMaleMiddle AgedTissue Array AnalysisBiomarkers, TumorChloride ChannelsCLCA2 protein, human

Identifiers

PMID25548429
PMCPMC4274868
OpenAlexW2115804548

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.