Evidence map›Paper›PMID 28540486›Full record

ArticlePathology oncology research : POR2018

The Expression of MCM7 is a Useful Biomarker in the Early Diagnostic of Gastric Cancer.

Jing-Yan Yang, Dong Li, Yuan Zhang, Bing-Xin Guan, Ping Gao, Xing-Chen Zhou, Cheng-Jun Zhou

Abstract read
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In one paragraph

Article in Pathology oncology research : POR, 2018. 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
1.3field-weighted citation impact, top 20% 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, 29 citations in OpenAlex.

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  12. Increased expression ofJournal of gastrointestinal oncology · 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

7 authors at 3 institutions in 1 country.

Jing-Yan YangDepartment of Pathology, The Second Hospital of Shandong University, 247#, BeiYuan Street, Jinan, Shandong, 250033, People's Republic of China.
Dong LiDepartment of Orthopedics, Shandong Provincial Hospital Affiliated to Shandong University, 324#, Jing 5 Road, Jinan, Shandong, 250021, People's Republic of China.
Yuan ZhangCenter of Evidence-based Medicine, The Second Hospital of Shandong University, 247#, BeiYuan Street, Jinan, Shandong, 250033, People's Republic of China.
Bing-Xin GuanDepartment of Pathology, The Second Hospital of Shandong University, 247#, BeiYuan Street, Jinan, Shandong, 250033, People's Republic of China.
Ping GaoYantai Affiliated Hospital of Binzhou Medical University, 717#, Jinbu Road, Muping District, Yantai, Shandong, 264100, People's Republic of China.
Xing-Chen ZhouDepartment of Pathology, The Second Hospital of Shandong University, 247#, BeiYuan Street, Jinan, Shandong, 250033, People's Republic of China.
Cheng-Jun ZhouDepartment of Pathology, The Second Hospital of Shandong University, 247#, BeiYuan Street, Jinan, Shandong, 250033, People's Republic of China. chengjunzhou@sdu.edu.cn.ORCID http://orcid.org/0000-0002-8359-3395
Second Hospital of Shandong University · CNBinzhou Medical University · CNShandong University · CN

Funding

Shandong Provincial Natural Science Foundation, China ZR2015HM036Youth Fund of the 2nd Hospital of Shandong University Y2015010044
6 · The paper itself

Abstract

The aim of this study was to investigate the expression of minichromosome maintenance complex component 7 (MCM7) in gastric mucosal lesions, further to find its potential effect as a biomarker to distinguish intraepithelial neoplasia from gastric mucosal lesions. MCM7 and Ki67 were detected in 93 cases of gastric mucosal lesions by immunohistochemistry. MCM7 and Ki67 expression in GT were lowest compared with other groups (P<0.001), meanwhile there were significant differences compared with Group IM and other groups in MCM7 and Ki67 expression (P<0.001). MCM7 and Ki67 expression in GSC were highest (P<0.05). Groups of LGN, HGN and GIC had no significant differences in MCM7 expression (P>0.05), but there was significant difference compared with Group LGN and Group GIC in Ki67 expression (P<0.05). MCM7 expression elevated with tumor grade increasing and had positive correlation with Ki67 significantly (r=0.940, P<0.001). Furthermore, in some cases, some tumor cells were immunoreactive to MCM7 but negative to Ki67. So we concluded that MCM7 is helpful for us to make differential diagnosis in pathological grade, MCM7 combination of Ki67 may serve as more sensitive proliferation markers for evaluation of gastric carcinoma and precancerous lesions.

Indexed as

AdenocarcinomaAdultAgedBiomarkers, TumorEarly Detection of CancerFemaleHumansKi-67 AntigenMaleMiddle AgedMinichromosome Maintenance Complex Component 7Neoplasm GradingPrecancerous ConditionsStomach NeoplasmsBiomarkers, TumorKi-67 AntigenMCM7 protein, humanMinichromosome Maintenance Complex Component 7Gastrointestinal epithelial neoplasiaIntestinal metaplasticKi67MCM7

Identifiers

PMID28540486
OpenAlexW2619028257

What OpenQuestion holds

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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.