Evidence map›Paper›PMID 26503471›Full record

SynthesisOncotarget2015

CD133 overexpression correlates with clinicopathological features of gastric cancer patients and its impact on survival: a systematic review and meta-analysis.

Li Yiming, Guo Yunshan, Ma Bo, Zang Yu, Wei Tao, Liang Gengfang, Fan Dexian, Cui Shiqian, Jiang Jianli, Tang Juan and 1 more

Open access · diamondAbstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 5 pooled it
4.0field-weighted citation impact, top 5% 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

36 citing papers in PubMed, 5 syntheses or guidelines pooled it, 59 citations in OpenAlex.

  1. Pooled it
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  6. Review
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  10. Can CD133 Be Regarded as a Prognostic Biomarker in Oncology: Pros and Cons.International journal of molecular sciences · 2023
    Review
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  17. Drug resistance and Cancer stem cells.Cell communication and signaling : CCS · 2021
    Review
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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

11 authors at 1 institution in 1 country.

Li YimingCell Engineering Research Centre, State Key Laboratory of Cancer Biology, The Fourth Military Medical University, Xi'an, Shaanxi, China.
Guo YunshanCell Engineering Research Centre, State Key Laboratory of Cancer Biology, The Fourth Military Medical University, Xi'an, Shaanxi, China.
Ma BoDepartment of Pharmacology, School of Pharmacy, The Fourth Military Medical University, Xi'an, Shaanxi, China.
Zang YuDepartment of Respiratory Disease, Tangdu Hospital, The Fourth Military Medical University, Xi'an, Shaanxi, China.
Wei TaoDepartment of Digestive Surgery, Huawan People Hospital, Zhuyang, Guangxi, China.
Liang GengfangDepartment of Digestive Surgery, Huawan People Hospital, Zhuyang, Guangxi, China.
Fan DexianDepartment of Digestive Surgery, Huawan People Hospital, Zhuyang, Guangxi, China.
Cui ShiqianDepartment of Digestive Surgery, Huawan People Hospital, Zhuyang, Guangxi, China.
Jiang JianliCell Engineering Research Centre, State Key Laboratory of Cancer Biology, The Fourth Military Medical University, Xi'an, Shaanxi, China.
Tang JuanCell Engineering Research Centre, State Key Laboratory of Cancer Biology, The Fourth Military Medical University, Xi'an, Shaanxi, China.
Chen ZhinanCell Engineering Research Centre, State Key Laboratory of Cancer Biology, The Fourth Military Medical University, Xi'an, Shaanxi, China.
Air Force Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCD133 is one of the most commonly used markers of cancer stem cells (CSCs), which are characterized by their ability for self-renewal and tumorigenicity. However, the clinical and prognostic significance of CD133 in gastric cancer remains controversial. To clarify a precise determinant of the clinical significance of CD133, we conducted a systematic review and meta-analysis to elucidate the correlation of CD133 overexpression with prognosis and clinicopathological features of GC patients.

methodsA search in the Cochrane Library, PubMed, Medline, Web of Knowledge and Chinese CNKI, CBM (up to Jun 30, 2015) was performed using the following keywords gastric cancer, CD133, AC133, prominin-1, etc. Electronic searches were supplemented by hand searching reference lists, abstracts and proceedings from meetings. Outcomes included overall survival and various clinicopathological features. Two reviewers independently screened the literature according to the inclusion and exclusion criteria, extracted the data, and assessed the methodological quality of the included studies, and then RevMan 5.2.0 software was used for meta-analysis.

resultsA total of 603 gastric cancer patients from 8 studies were included. The results of the meta-analyses showed that, there were significant differences of CD133 expression in the following comparisons: gastric cancer tissues vs. normal esophageal tissue (OR = 3.49, 95% CI [2.48, 490], P < 0.00001), lymph node metastasis vs. non-lymph node metastasis (OR = 2.75, 95% CI [1.99, 3.81], P < 0.00001), distant metastasis vs. non-distant metastasis (OR = 2.38, 95%CI [1.47, 3.85], P < 0.0004), clinical stages III~IV vs. clinical stages I~II (OR = 2.83, 95% CI [2.13, 3.76], P < 0.00001), as well as the accumulative 5-year overall survival rates of CD133-positive vs. CD133-negative patients (OR = 0.23, 95% CI [0.16, 0.33], P < 0.00001).

conclusionOverexpression of CD133 is associated with lymph node metastasis, distant metastasis, poor TNM stage. Additionally, CD133-positive gastric cancer patients had worse prognosis. Our results indicate that CD133 may be involved in the carcinogenesis of gastric cancer. Evaluation of cytoplasmic CD133 overexpression in gastric cancer tissue sections may be useful in the future as a novel prognostic factor. Nevertheless, due to the poor quality and small sample size of included trials, more well-designed multi-center randomized controlled trials should be performed.

Indexed as

AC133 AntigenAntigens, CDFemaleGlycoproteinsHumansImmunohistochemistryMaleNeoplasm MetastasisNeoplasm StagingPeptidesPrognosisStomach NeoplasmsSurvival AnalysisAC133 AntigenAntigens, CDGlycoproteinsPeptidesPROM1 protein, humanCD133CSCgastric cancerIHC

Identifiers

PMID26503471
PMCPMC4747206
OpenAlexW1959431242

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.