Evidence map›Paper›PMID 25527865›Full record

ArticleJournal of experimental & clinical cancer research : CR2014

Detection of ALK protein expression in lung squamous cell carcinomas by immunohistochemistry.

Jiandong Wang, Qin Shen, Qunli Shi, Bo Yu, Xuan Wang, Kai Cheng, Guangming Lu, Xiaojun Zhou

Open access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 15% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

  1. Pooled it
  2. Trial
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  12. [A Case of Advanced Lung Squamous Cell Carcinoma with CLIP1-ALK Fusion Gene].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2022
    Article
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  16. [Progress in Treatment of Advanced Squamous Cell Lung Cancer].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2020
    Review
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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

8 authors at 1 institution in 1 country.

Jiandong WangDepartment of Pathology, Jinling Hospital, Nanjing University School of Medicine, Nanjing, 210002, China. jd_wang@outlook.com.
Qin ShenDepartment of Pathology, Jinling Hospital, Nanjing University School of Medicine, Nanjing, 210002, China. jd_wang@outlook.com.
Qunli ShiDepartment of Pathology, Jinling Hospital, Nanjing University School of Medicine, Nanjing, 210002, China. shiqunli2005@aliyun.com.
Bo YuDepartment of Pathology, Jinling Hospital, Nanjing University School of Medicine, Nanjing, 210002, China. 9441698@qq.com.
Xuan WangDepartment of Pathology, Jinling Hospital, Nanjing University School of Medicine, Nanjing, 210002, China. wangxuan1130@163.com.
Kai ChengDepartment of Pathology, Jinling Hospital, Nanjing University School of Medicine, Nanjing, 210002, China. chengkai_seu@126.com.
Guangming LuDepartment of Radiology, Jinling Hospital, Nanjing University School of Medicine, Nanjing, 210002, China. cjr.luguangming@vip.163.com.
Xiaojun ZhouDepartment of Pathology, Jinling Hospital, Nanjing University School of Medicine, Nanjing, 210002, China. nanjing_81@yahoo.com.
Nanjing University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe echinoderm microtubule-associated protein-like 4 (EML4) gene and the anaplastic lymphoma kinase (ALK) gene rearrangements occur in approximately 5% of lung adenocarcimomas (ACA), leading to ALK overexpression and predicting response to targeted therapy. To the present, few studies have been focused on the expression of ALK protein in lung squamous cell carcinomas (SqCC). Only several cases of lung SqCC were reported expression of ALK protein. No clinical study has been published to explicit the relationship between ALK expression and the response to targeted therapy in SqCC.

methodsIn this study, we analyzed ALK protein expression with a specific rabbit monoclonal Ig antibody (D5F3 clone) in 207 cases of lung SqCC. The positive cases were confirmed with ALK fluorescence in situ hybridization (FISH) and RT-PCR.

resultsWe found that 3 out of 207 (1.4%) cases of lung SqCC were ALK positive detected by IHC staining, which were confirmed by ALK FISH and RT-PCR.

conclusionsOur results indicate that ALK protein expression is not a rare molecular event in SqCC. Although the frequency of EML4-ALK rearrangements is lower in lung SqCC than that in lung adenocarcinomas, their presence may provide additional treatment options in lung SqCC. The response of SqCC patients with ALK expression to target therapy of crizotinib should be explored.

Indexed as

ImmunohistochemistryAdultAgedAged, 80 and overAnaplastic Lymphoma KinaseBiomarkers, TumorCarcinoma, Squamous CellFemaleGene RearrangementHumansIn Situ Hybridization, FluorescenceLung NeoplasmsMaleMiddle AgedOncogene Proteins, FusionReceptor Protein-Tyrosine KinasesALK protein, humanAnaplastic Lymphoma KinaseBiomarkers, TumorEML4-ALK fusion protein, humanOncogene Proteins, FusionReceptor Protein-Tyrosine Kinases

Identifiers

PMID25527865
PMCPMC4304180
OpenAlexW2130588193

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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.