Evidence map›Paper›PMID 26045824›Full record

ArticleInternational journal of clinical and experimental pathology2015

High expression of E-cadherin in pleural effusion cells predicts better prognosis in lung adenocarcinoma patients.

Chao Zhao, Xuefei Li, Chunxia Su, Jiayu Li, Ningning Cheng, Shengxiang Ren, Xiaoxia Chen, Caicun Zhou

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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 25% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. TWIST1 upregulation affects E-cadherin expression in brain metastases.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2021
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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 2 institutions in 1 country.

Chao ZhaoDepartment of Lung Cancer and Immunology, Shanghai Pulmonary Hospital, Tongji University; Tongji University Medical School Cancer Institute No. 507 Zhengmin Road, Shanghai 200433, People's Republic of China.
Xuefei LiDepartment of Lung Cancer and Immunology, Shanghai Pulmonary Hospital, Tongji University; Tongji University Medical School Cancer Institute No. 507 Zhengmin Road, Shanghai 200433, People's Republic of China.
Chunxia SuShanghai Pulmonary Hospital, Tongji University No. 507 Zhengmin Road, Shanghai 200433, People's Republic of China.
Jiayu LiShanghai Pulmonary Hospital, Tongji University No. 507 Zhengmin Road, Shanghai 200433, People's Republic of China.
Ningning ChengShanghai Pulmonary Hospital, Tongji University No. 507 Zhengmin Road, Shanghai 200433, People's Republic of China.
Shengxiang RenShanghai Pulmonary Hospital, Tongji University No. 507 Zhengmin Road, Shanghai 200433, People's Republic of China.
Xiaoxia ChenShanghai Pulmonary Hospital, Tongji University No. 507 Zhengmin Road, Shanghai 200433, People's Republic of China.
Caicun ZhouShanghai Pulmonary Hospital, Tongji University No. 507 Zhengmin Road, Shanghai 200433, People's Republic of China.
Shanghai Pulmonary Hospital · CNTongji University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEpithelial-mesenchymal transition (EMT) is of great importance in tumor metastasis. Our previous study demonstrates that epithelial phenotype is related to epidermal growth factor receptor (EGFR) mutation and the sensitivity of EGFR tyrosine kinase inhibitors (TKIs) in advanced non-small cell lung cancer (NSCLC) patients. However, the role of EMT phenotype in malignant pleural effusions in predicting prognosis is unknown in lung adenocarcinoma patients.

methodPleural effusions of lung adenocarcinoma patients were collected and made into cell block (CB). EGFR mutation was detected using amplification refractory mutation system (ARMS) PCR method and H-score system was applied to evaluate the staining intensity of EMT marker and tumor cell ratio.

resultsForty-three CB samples, including 22 samples before any treatment (baseline, group 1) and 21 with disease progression (group 2) after first-line chemotherapy, were enrolled in this study. The expression of N-cadherin and vimentin were low in the CB tumor cells. There was no significant difference in the tumor cell radio and E-cadherin expression in the two groups. E-cadherin expression had no association with sex, age and smoking status and also patient response in both the two groups. However, high E-cadherin expression was related to EGFR mutation (P=0.032) and long progression-free survival (PFS) (P=0.015) in group 1 but not group 2 samples.

conclusionE-cadherin expression in CB samples was associated with EGFR mutation status and patient prognosis in lung adenocarcinoma patients in first-line chemotherapy.

Indexed as

AdenocarcinomaAgedBiomarkers, TumorCadherinsDisease-Free SurvivalDNA Mutational AnalysisEpithelial-Mesenchymal TransitionFemaleGenes, erbB-1HumansImmunohistochemistryKaplan-Meier EstimateLung NeoplasmsMaleMiddle AgedMutationBiomarkers, TumorCadherinscell blockEGFREMTnon-small cell lung cancer

Identifiers

PMID26045824
PMCPMC4440133
OpenAlexW2415462296

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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.