Evidence map›Paper›PMID 41266092›Full record

ArticleJournal of Yeungnam medical science2025

ETS-related gene as a key factor in curcumin inhibition of glucose metabolism in prostate cancer cells: an in vitro experimental study.

Yunye Wang, Xingyu Zhao, Jierui Zhao, Xin Wang, Yumiao Guo, Shutong Chen, Ying Jin, Peng Peng, Wei Zhang

Abstract read
In one paragraph

Article in Journal of Yeungnam medical science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Review
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

9 authors.

Yunye WangDepartment of Basic Medical Sciences, Jilin Medical University, Jilin, China.
Xingyu ZhaoDepartment of Basic Medical Sciences, Jilin Medical University, Jilin, China.
Jierui ZhaoDepartment of Chinese Medicine, Macau University of Science and Technology, Macau, China.
Xin WangDepartment of Basic Medical Sciences, Jilin Medical University, Jilin, China.
Yumiao GuoDepartment of Basic Medical Sciences, Yanbian Medical University, Yanji, China.
Shutong ChenDepartment of Basic Medical Sciences, Beihua Medical University, Jilin, China.
Ying JinDepartment of Basic Medical Sciences, Jilin Medical University, Jilin, China.
Peng PengDepartment of Chinese Medicine, Macau University of Science and Technology, Macau, China.
Wei ZhangDepartment of Basic Medical Sciences, Jilin Medical University, Jilin, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCurcumin, the main yellow pigment in turmeric, is a potent anticancer agent. However, its effect on the viability of human prostate cancer (PCa) cells and underlying mechanisms remain unclear. This study aimed to determine the effects of curcumin on the proliferation and glucose metabolism of PCa cells.

methodsCell viability was measured by MTS assay, and apoptosis was measured by flow cytometry. Glucose metabolism was assessed by measuring glucose intake, lactate production, and adenosine triphosphate content. Western blotting was performed to detect the expression of apoptosis-related proteins.

resultsCurcumin treatment significantly reduced the viability of two types of PCa cells. We also found that curcumin increased apoptosis and glycolysis by inhibiting the activities of phosphatidylinositol 3-kinase/protein kinase B and hypoxia-inducible factor-1α. Furthermore, curcumin reduced the expression of ETS-related gene (ERG). However, after the ERG was knocked out, the effects of curcumin treatment were attenuated.

conclusionThis study investigated the effects of curcumin on the proliferation and apoptosis of PCa cells, which may be related to the inhibition of glycolysis, and further explored the pathway involved. The subsequent effect on ERG expression indicated that these effects may be related to this oncogene.

Indexed as

ApoptosisCurcuminERGGlycolysisProstatic neoplasms

Identifiers

PMID41266092
PMCPMC12800555

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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.