Evidence map›Paper›PMID 31847250›Full record

ArticleToxins2019

The Cytotoxicity Effect of Resveratrol: Cell Cycle Arrest and Induced Apoptosis of Breast Cancer 4T1 Cells.

Hong Wu, Liang Chen, Feifei Zhu, Xu Han, Lindan Sun, Keping Chen

Open access · goldAbstract read
In one paragraph

Article in Toxins, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 86 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
86citing papers in PubMed, 3 pooled it
8.0field-weighted citation impact, top 1% 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

86 citing papers in PubMed, 3 syntheses or guidelines pooled it, 184 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. The Invasive SpeciesFrontiers in pharmacology · 2022
    Pooled it
  4. Review
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  9. Review
  10. Astragaloside IV AlleviatesAntioxidants (Basel, Switzerland) · 2026
    Article
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  14. Review
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  17. Article
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26 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

6 authors at 1 institution in 1 country.

Hong WuInstitute of Life Sciences, Jiangsu University, 301 Xuefu Road, Zhenjiang 212013, China.
Liang ChenInstitute of Life Sciences, Jiangsu University, 301 Xuefu Road, Zhenjiang 212013, China.
Feifei ZhuInstitute of Life Sciences, Jiangsu University, 301 Xuefu Road, Zhenjiang 212013, China.
Xu HanInstitute of Life Sciences, Jiangsu University, 301 Xuefu Road, Zhenjiang 212013, China.
Lindan SunInstitute of Life Sciences, Jiangsu University, 301 Xuefu Road, Zhenjiang 212013, China.
Keping ChenInstitute of Life Sciences, Jiangsu University, 301 Xuefu Road, Zhenjiang 212013, China.ORCID 0000-0001-5254-2299
Jiangsu University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Resveratrol, a natural polyterpenoid, can scavenge reactive oxygen species in vivo to carry out the functions of antioxidation and antiaging. Resveratrol's anti-cancer capability has attracted widespread attention, but its molecular mechanism has not been systematically explained. In this study, by comparing the activity of normal cell lines and cancer cell lines after treating with resveratrol, it was found that resveratrol has more significant cytotoxicity in cancer cell lines. Resveratrol could play a toxic role through inducing apoptosis of the cancer cell in a time- and concentration-dependent manner. A total of 330 significantly differential genes were identified through large-scale transcriptome sequencing, among which 103 genes were upregulated and 227 genes were downregulated. Transcriptome and qRT-PCR data proved that a large number of genes related to cell cycle were differentially expressed after the treatment of resveratrol. The changes of cell cycle phases at different time points after treating with resveratrol were further detected, and it was found that the cells were arrested in the S phase because of the percentage of cells in S phase increased and cells in G1/G0 phase decreased. In conclusion, resveratrol can inhibit the proliferation of 4T1 cancer cells by inhibiting cell cycle and inducing apoptosis.

Indexed as

Antineoplastic AgentsApoptosisBreast NeoplasmsCell Cycle CheckpointsCell LineGene Expression ProfilingGene Expression Regulation, NeoplasticHumansResveratrolAntineoplastic AgentsResveratrolapoptosiscell cyclecytotoxicityresveratrolRNA-seq

Identifiers

PMID31847250
PMCPMC6950385
OpenAlexW2999534237

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.