Evidence map›Paper›PMID 38984567›Full record

ArticleAnti-cancer agents in medicinal chemistry2024

The Growth Inhibitory Effect of Resveratrol and Gallic Acid on Prostate Cancer Cell Lines through the Alteration of Oxidative Stress Balance: The Interplay between

Delaram Moghadam, Reza Zarei, Amirabbas Rostami, Mohammad Samare-Najaf, Rozita Ghojoghi, Amir Savardashtaki, Morteza Jafarinia, Sina Vakili, Cambyz Irajie

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Article in Anti-cancer agents in medicinal chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. 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

9 authors.

Delaram MoghadamAutophagy Research Center, Department of Biochemistry, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.ORCID 0000-0001-9593-3919
Reza ZareiAutophagy Research Center, Department of Biochemistry, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.ORCID 0000-0002-6830-0750
Amirabbas RostamiDepartment of Internal Medicine, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Mohammad Samare-NajafAutophagy Research Center, Department of Biochemistry, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.ORCID 0000-0002-1741-503X
Rozita GhojoghiDepartment of Bacteriology and Virology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Amir SavardashtakiDepartment of Medical Biotechnology, School of Advanced Medical Sciences and Technologies, Shiraz University of Medical Sciences, Shiraz, Iran.ORCID 0000-0003-1700-9426
Morteza JafariniaShiraz Neuroscience Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.ORCID 0000-0002-3272-448X
Sina VakiliInfertility Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.ORCID 0000-0002-5472-8350
Cambyz IrajieDepartment of Medical Biotechnology, School of Advanced Medical Sciences and Technologies, Shiraz University of Medical Sciences, Shiraz, Iran.ORCID 0000-0001-8438-2146

Funding

Shiraz University of Medical Sciences 23985,23985
6 · The paper itself

Abstract

backgroundThe association between oxidative stress and prostate cancer (PC) has been demonstrated both epidemiologically and experimentally. Balance in reactive oxygen species (ROS) levels depends on multiple factors, such as the expression of

objectiveThe present study investigated the possible effects of GA and RSV on the oxidative profiles of PC3 and DU145 cells, as well as

methodsPC3 and DU145 cells were treated with ascending concentrations of RSV and GA for 72 h. Then cell growth and mRNA expression of

resultsRSV and GA significantly decreased the growth of PC3 and DU145 cells compared to the control group in a concentration-dependent manner. RSV and GA also decreased ROS production in PC3 cells, but in DU145 cells, only the latter polyphenol significantly decreased ROS content. In addition, RSV and GA had ameliorating effects on SOD, GR, GPX, and CAT activities and GSH levels in both cell lines. Also, RSV and GA induced HO- 1 and Nrf2 gene expression in both cell lines. BACH1 gene expression was induced by RSV only at lower concentrations, in contrast to GA in both cell lines.

conclusionOur data suggest that RSV and GA can prevent the growth of prostate cancer cells by disrupting oxidative stress-related pathways, such as changes in

Indexed as

Basic-Leucine Zipper Transcription FactorsCell ProliferationDose-Response Relationship, DrugGallic AcidNF-E2-Related Factor 2Oxidative StressProstatic NeoplasmsResveratrolAntineoplastic AgentsCell SurvivalDrug Screening Assays, AntitumorHeme Oxygenase-1HumansMaleMolecular StructureReactive Oxygen SpeciesAntineoplastic AgentsBACH1 protein, humanBasic-Leucine Zipper Transcription FactorsGallic AcidHeme Oxygenase-1HMOX1 protein, humanNFE2L2 protein, humanNF-E2-Related Factor 2Reactive Oxygen SpeciesResveratrolBACH1.HO-1Nrf2oxidative stresspolyphenolsProstate cancer

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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.