Evidence map›Paper›PMID 31933993›Full record

ArticleInternational journal of clinical and experimental pathology2019

Evaluation of the correlativity of gender determining region Y-box 4, N-cadherin, CD44 and E-cadherin expression in the prognosis of esophageal squamous cell carcinoma.

Yanzi Qin, Wenjun Zhao, Lili Cheng, Jin Gao, Zhaonan Bian, Shiwu Wu, Zenong Cheng, Yisheng Tao, Li Ma

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2019. 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
0.1field-weighted citation impact, top 45% 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

9 authors at 1 institution in 1 country.

Yanzi QinDepartment of Pathology, The First Affiliated Hospital of Bengbu Medical College, Bengbu Medical College Bengbu 233003, Anhui Province, China.
Wenjun ZhaoDepartment of Emergency Internal Medicine, The First Affiliated Hospital of Bengbu Medical College, Bengbu Medical College Bengbu 233003, Anhui Province, China.
Lili ChengDepartment of Pathology, The First Affiliated Hospital of Bengbu Medical College, Bengbu Medical College Bengbu 233003, Anhui Province, China.
Jin GaoDepartment of Clinical Medicine, Bengbu Medical College Anhui Province, China.
Zhaonan BianDepartment of Clinical Medicine, Bengbu Medical College Anhui Province, China.
Shiwu WuDepartment of Pathology, The First Affiliated Hospital of Bengbu Medical College, Bengbu Medical College Bengbu 233003, Anhui Province, China.
Zenong ChengDepartment of Pathology, The First Affiliated Hospital of Bengbu Medical College, Bengbu Medical College Bengbu 233003, Anhui Province, China.
Yisheng TaoDepartment of Pathology, The First Affiliated Hospital of Bengbu Medical College, Bengbu Medical College Bengbu 233003, Anhui Province, China.
Li MaDepartment of Pathology, The First Affiliated Hospital of Bengbu Medical College, Bengbu Medical College Bengbu 233003, Anhui Province, China.
Bengbu Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSOX4 is highly expressed in many different tumor types, and SOX4 has been reported in the literature to participate in tumor proliferation, damaging and movement by leading Epithelial-Mesenchymal Transition. Cancer vital cells and Epithelial-Mesenchymal Transition have been repeatedly confirmed to participate during the proliferation, damaging and movement of cancer. This research examined the association of the Epithelial-Mesenchymal Transition-related molecules E-cadherin, N-cadherin, CD44, and SOX4 in the ESCC and aimed for providing inspiration for clinical treatment as well as to indicate a new direction for detecting invasion and forecasting the prospect of affected role using ESCC.

methodsImmunohistochemistry was utilized to observe the expression of the S0X4, N-cadherin, CD44 and E-cadherin proteins. Survival analysis of the positive and negative SOX4, E-cadherin, N-cadherin and CD44 protein expression groups was performed by the Kaplan-Meier approach. OUTCOMES: A confirming relationship was observed among the expression of SOX4, N-cadherin or CD44 and tumor diameter, distant metastasis, deepness of damaging, lymph node metastasis, pTNM stage and histological grade (

conclusionsWe found that suppression of ESCC providers can suppress the growth of bad tumors and change therapeutic results for ESCC patient since CD44 supports the induction of Epithelial-Mesenchymal Transition in ESCC.

Indexed as

CD44E-cadherinESCCN-cadherinSOX4

Identifiers

PMID31933993
PMCPMC6947138
OpenAlexW3027727589

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.