Evidence map›Paper›PMID 25120788›Full record

ArticleInternational journal of clinical and experimental pathology2014

Transcription factors related to epithelial mesenchymal transition in tumor center and margin in invasive lung adenocarcinoma.

Young-In Maeng, Kyung-Hyun Kim, Jung-Yeon Kim, Sun-Jae Lee, Woo-Jung Sung, Chong-Kee Lee, Jae-Bok Park, Kwan-Kyu Park

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Clinical significance of epithelial-mesenchymal transition-related markers expression in the micrometastatic sentinel lymph node of NSCLC.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2020
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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.

Young-In MaengDepartment of Pathology, School of Medicine, Catholic University of Daegu Daegu, Republic of Korea.
Kyung-Hyun KimDepartment of Pathology, School of Medicine, Catholic University of Daegu Daegu, Republic of Korea.
Jung-Yeon KimDepartment of Pathology, School of Medicine, Catholic University of Daegu Daegu, Republic of Korea.
Sun-Jae LeeDepartment of Pathology, School of Medicine, Catholic University of Daegu Daegu, Republic of Korea.
Woo-Jung SungDepartment of Pathology, School of Medicine, Catholic University of Daegu Daegu, Republic of Korea.
Chong-Kee LeeDepartment of Immunology, School of Medicine, Catholic University of Daegu Daegu, Republic of Korea.
Jae-Bok ParkDepartment of Pathology, School of Medicine, Catholic University of Daegu Daegu, Republic of Korea.
Kwan-Kyu ParkDepartment of Pathology, School of Medicine, Catholic University of Daegu Daegu, Republic of Korea.
Daegu Catholic University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The tumor microenvironment has many roles involving tumor progression, invasion and metastasis. The tumor cells at the tumor border loose epithelial properties and acquire mesenchymal features. This, epithelial-to-mesenchymal transition (EMT) has been suggested to be an important process for tissue and lymphovascular invasion. Pulmonary tissue samples from 15 patients with primary adenocarcinoma were evaluated with using immunofluorescence multi-staining the EMT-associated markers including E-cadherin and alpha-smooth muscle actin (α-SMA), and transcription factors including E-SNAIL and SLUG, and ZEB1. The data were analyzed in specific area, such as tumor center and tumor border. In this study we show that the invasive adenocarcinoma differentially expressed SNAIL and SLUG, and Zeb1 and it was associated with the loss of epithelial marker (E-cadherin) and gaining of mesenchymal marker (α-SMA) at the invasive border of lung carcinoma. The positive rates of SNAIL and ZEB1 were 26.7% and 0% in the tumor center and 40% and 20% in tumor margin, respectively. In addition, the expression of both SNAIL and ZEB1 at the border of tumor was observed in two cases (2/10). These two cases were associated with lymph node metastasis and advanced stage. The process of EMT has been suggested to be of prime importance for tissue and lymphovascular invasion. The process of EMT may be activated in the tumor border of lung adenocarcinoma. Related transcription factors, such as SNAIL and SLUG, and ZEB1, might be induced by paracrine effects of surrounded inflammatory cells and fibroblasts.

Indexed as

ActinsAdenocarcinomaAdenocarcinoma of LungAgedAged, 80 and overBiomarkers, TumorCadherinsEpithelial-Mesenchymal TransitionFemaleFluorescent Antibody TechniqueHomeodomain ProteinsHumansLung NeoplasmsMaleMiddle AgedRetrospective StudiesActinsBiomarkers, TumorCadherinsHomeodomain ProteinsSNAI1 protein, humanSnail Family Transcription FactorsTranscription FactorsZEB1 protein, humanZinc Finger E-box-Binding Homeobox 1Epithelial mesenchymal transitionlung adenocarcinomaSLUGSNAILZEB1

Identifiers

PMID25120788
PMCPMC4129023
OpenAlexW1929638171

What OpenQuestion holds

Textmetadata
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.