Evidence map›Paper›PMID 25400739›Full record

ArticleInternational journal of clinical and experimental pathology2014

Expression of SNCG, MAP2, SDF-1 and CXCR4 in gastric adenocarcinoma and their clinical significance.

Shufang Zheng, Lifang Shi, Yi Zhang, Tao He

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 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.6field-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

17 citing papers in PubMed, 25 citations in OpenAlex.

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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

4 authors at 2 institutions in 1 country.

Shufang ZhengDepartment of Pathology, Affiliated Hospital of Logistics College of The Chinese People's Armed Police Force 220 Chenglin Road, Hedong District, Tianjin 300162, People's Republic of China.
Lifang ShiDepartment of Pathology, Affiliated Hospital of Logistics College of The Chinese People's Armed Police Force 220 Chenglin Road, Hedong District, Tianjin 300162, People's Republic of China.
Yi ZhangPostgraduate Training Center for Liaoning Medical College in Affiliated Hospital of Logistics College, The Chinese People's Armed Police Force 220 Chenglin Road, Hedong District, Tianjin 300162, People's Republic of China.
Tao HeDepartment of Pathology, Affiliated Hospital of Logistics College of The Chinese People's Armed Police Force 220 Chenglin Road, Hedong District, Tianjin 300162, People's Republic of China.
Logistics University of People's Armed Police Force · CNChinese People's Armed Police Force Medical College Affiliated Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe purpose of the study was to detect the expression of SNCG, MAP2, SDF-1 and CXCR4 in gastric adenocarcinoma, and to evaluate their roles in the carcinogenesis of gastric adenocarcinoma, development, invasion and metastasis as well as their clinical significance.

methodsThe expression of SNCG, MAP2, SDF-1 and CXCR4 was detected by SP immunohistochemical method in 225 cases of gastric adenocarcinoma and 105 cases of nonneoplastic adjacent gastric tissue. The expression of SNCG, MAP2, SDF-1 and CXCR4 mRNA was also detected by RT-PCR method in 50 cases of gastric adenocarcinoma and 30 cases of nonneoplastic adjacent gastric tissue.

resultsThe expression of SNCG, MAP2, SDF-1 and CXCR4 in the gastric adenocarcinoma was remarkably higher than those in the nonneoplastic adjacent gastric tissue (P < 0.01); The positive expression of SNCG and MAP2 was correlated with the depth of tumor invasion and the metastasis of lymph nodes (P < 0.05), and that of SDF-1 and CXCR4 was correlated with the metastasis of lymph nodes (P < 0.05).

conclusionsSNCG, MAP2, SDF-1 and CXCR4 may play an important role in the carcinogenesis, progression, invasion and metastasis of gastric adenocarcinoma. However, it still needs more exploration whether they can serve as promising therapeutic targets of gastric adenocarcinoma.

Indexed as

AdenocarcinomaBiomarkers, TumorCase-Control StudiesChemokine CXCL12Disease ProgressionFemalegamma-SynucleinHumansImmunohistochemistryLymphatic MetastasisMaleMicrotubule-Associated ProteinsMiddle AgedNeoplasm InvasivenessNeoplasm ProteinsReceptors, CXCR4Biomarkers, TumorChemokine CXCL12CXCL12 protein, humanCXCR4 protein, humangamma-SynucleinMAP2 protein, humanMicrotubule-Associated ProteinsNeoplasm ProteinsReceptors, CXCR4RNA, MessengerSNCG protein, humanCXCR4gastric adenocarcinomaimmunohistochemistryMAP2RT-PCRSDF-1SNCG

Identifiers

PMID25400739
PMCPMC4230097
OpenAlexW228859894

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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.