Evidence map›Paper›PMID 21829201›Full record

ArticleBritish journal of cancer2011

Sequential expression of putative stem cell markers in gastric carcinogenesis.

T Wang, C W Ong, J Shi, S Srivastava, B Yan, C L Cheng, W P Yong, S L Chan, K G Yeoh, B Iacopetta and 1 more

Open access · hybridAbstract readEvaluation Study
In one paragraph

Article in British journal of cancer, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed, 2 pooled it
4.5field-weighted citation impact, top 4% 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

74 citing papers in PubMed, 2 syntheses or guidelines pooled it, 112 citations in OpenAlex.

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  12. FTO-mediated mJournal of cancer research and clinical oncology · 2023
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  17. Increased CD44 Expression and MEK Activity Predict Worse Prognosis in Gastric Adenocarcinoma Patients Undergoing Gastrectomy.Journal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract · 2021
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14 more citing papers are in PubMed but not listed here.

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

11 authors at 3 institutions in 2 countries.

T WangCancer Science Institute, National University Health System and Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
C W Ong
J Shi
S Srivastava
B Yan
C L Cheng
W P Yong
S L Chan
K G Yeoh
B Iacopetta
M Salto-Tellez
National University of Singapore · SGNational University Health System · SGUniversity of Western Australia · AU

Funding

NIMH NIH HHS MH 9503/22
6 · The paper itself

Abstract

backgroundGastric carcinogenesis has been well documented in the step-wise histopathological model, known as Correa pathway. Several biomarkers including CD44, Musashi-1 and CD133 have been reported as putative stem cell (PSC) markers.

methodsWe investigated expression of PSC markers CD44, Musashi-1 and CD133 in relation to gastric carcinogenesis and prognosis and chemoresponse. Immunohistochemistry staining was performed in gastric cancer (GC) clinical specimens representing different steps of the Correa pathway. Gastric cancer samples taken before and after neoadjuvant chemotherapy with docetaxel, cisplatin and capecitabine (DCX) were also evaluated for PSC marker expression.

resultsWe showed that the expression of three PSC markers was significantly elevated in GC relative to normal gastric mucosa (P<0.001 for each marker). Precancerous lesions, including intestinal metaplasia and dysplasia, demonstrated increased expression of CD44 and Musashi-1. CD133 was predominantly expressed along the border between intramucosal carcinoma and connective tissue at later stages. High CD44 and CD133 expression showed prognostic value for worse patient survival (P=0.014 and P=0.019, respectively). A small number of tumours with high expression of CD44 and CD133 showed pathological response to DCX-based neoadjuvant chemotherapy.

conclusionCD44 and Musashi-1 are frequently expressed in both premalignant gastric lesions and invasive GC, whereas CD133 expression is restricted mainly to neoplastic tissues.

Indexed as

AC133 AntigenAdultAgedAged, 80 and overAntigens, CDAntineoplastic Combined Chemotherapy ProtocolsBiomarkers, PharmacologicalBiomarkers, TumorCarcinomaClinical Trials, Phase II as TopicFemaleGene Expression Regulation, NeoplasticGlycoproteinsHumansHyaluronan ReceptorsImmunohistochemistryAC133 AntigenAntigens, CDBiomarkers, PharmacologicalBiomarkers, TumorCD44 protein, humanGlycoproteinsHyaluronan ReceptorsMSI1 protein, humanNerve Tissue ProteinsPeptidesPROM1 protein, humanRNA-Binding Proteins

Identifiers

PMID21829201
PMCPMC3188930
OpenAlexW1990877484

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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.