Evidence map›Paper›PMID 28052033›Full record

SynthesisOncotarget2017

GLUT-1 overexpression as an unfavorable prognostic biomarker in patients with colorectal cancer.

Jing Yang, Jing Wen, Tian Tian, Zhongsheng Lu, Yao Wang, Zikai Wang, Xiangdong Wang, Yunsheng Yang

Registry-linked trialOpen access · diamondAbstract readMeta-Analysis
In one paragraph

Synthesis in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03467308 (Identification of New Signaling Pathways Targeting Colorectal Cancer in Egyptian Patients), which is not on this map. Cited by 46 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 4 pooled it
3.3field-weighted citation impact, top 7% 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.

NCT03467308 completednot on this mapstarted 2018, after this paper: background citation

Identification of New Signaling Pathways Targeting Colorectal Cancer in Egyptian Patients

TypeobservationalSponsorAssiut UniversityRan2018 to 2020Enrolled180ConditionsColorectal CancerArmsMarkers in tissue samples: (TIGAR , TRIM59, P53, AKT, GSH)
3 · Its place in the literature

Who cites it

46 citing papers in PubMed, 4 syntheses or guidelines pooled it, 69 citations in OpenAlex.

  1. Pooled it
  2. Effect of blood glucose level on standardized uptake value (SUV) inEuropean journal of nuclear medicine and molecular imaging · 2019
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  15. Targeting the Warburg Effect in Cancer: Where Do We Stand?International journal of molecular sciences · 2024
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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

8 authors at 2 institutions in 1 country.

Jing YangDepartment of Gastroenterology and Hepatology, Chinese PLA General Hospital, Beijing, China.
Jing WenDepartment of Gastroenterology and Hepatology, Chinese PLA 261 Hospital, Beijing, China.
Tian TianNanlou Department of Respiratory Disease, Chinese PLA General Hospital, Beijing, China.
Zhongsheng LuDepartment of Gastroenterology and Hepatology, Chinese PLA General Hospital, Beijing, China.
Yao WangDepartment of Immunology/Bio-therapeutic, Institute of Basic Medicine, Chinese PLA General Hospital, Beijing, China.
Zikai WangDepartment of Gastroenterology and Hepatology, Chinese PLA General Hospital, Beijing, China.
Xiangdong WangDepartment of Gastroenterology and Hepatology, Chinese PLA General Hospital, Beijing, China.
Yunsheng YangDepartment of Gastroenterology and Hepatology, Chinese PLA General Hospital, Beijing, China.
Chinese PLA General Hospital · CNPLA 306 Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGlucose transporter-1 (GLUT-1) exhibits altered expression in colorectal cancer (CRC). The aim of this study was to explore the association between GLUT-1 and survival conditions, as well as clinical features in CRC by meta-analysis. MATERIALS AND

methodsRelevant studies were searched through predefined strategies, hazard ratios (HRs), odds ratios (ORs), and their 95% confidence intervals (CIs) were used as effective measures.

resultsA total of 14 studies with 2,077 patients were included in this meta-analysis. The results showed that GLUT-1 was not significantly associated with overall survival (OS) (HR=1.28, 95% CI=0.86-1.91, p=0.22) or disease-free survival (DFS) (HR=1.71, 95% CI=0.78-3.72, p=0.179). However, subgroup analysis indicated that GLUT-1 was a significant biomarker for poor DFS in rectal cancer (HR=2.47, 95% CI=1.21-5.05, p=0.013). GLUT-1 expression was also found to be significantly correlated with the presence of lymph node metastasis (n=8, OR=2.14, 95% CI=1.66-2.75, p<0.001), T stage (n=6, OR=1.73, 95% CI=1.17-2.58, p=0.007), higher Dukes stage (n=5, OR=2.92, 95% CI=2.16-3.95, p<0.001), female sex (n=4, OR=2.92, 95% CI=2.16-3.95, p<0.001), and presence of liver metastasis (n=3, OR=1.82, 95% CI=1.06-3.12, p=0.03).

conclusionIn conclusion, this meta-analysis showed that GLUT-1 was associated with poor DFS in rectal cancer (RC). Furthermore, GLUT-1 was also an indicator of aggressive clinical features in CRC.

Indexed as

Colorectal NeoplasmsGlucose Transporter Type 1HumansPrognosisSurvival AnalysisGlucose Transporter Type 1SLC2A1 protein, humanbiomarkercolorectal cancerGLUT-1meta-analysissurvival

Identifiers

PMID28052033
PMCPMC5355304
OpenAlexW2563079238

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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.