Evidence map›Paper›PMID 31464618›Full record

ArticleBMC complementary and alternative medicine2019

Resveratrol induces apoptosis of benign prostatic hyperplasia epithelial cell line (BPH-1) through p38 MAPK-FOXO3a pathway.

Chao Li, Wan-Li Hu, Meng-Xin Lu, Guan-Fa Xiao

Open access · goldAbstract read
In one paragraph

Article in BMC complementary and alternative medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

19 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Review
  3. Food science & nutrition · 2026
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  7. Article
  8. Article
  9. Nutrients · 2023
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  10. Review
  11. Effects of red ginseng oil(KGC11Journal of ginseng research · 2022
    Article
  12. Article
  13. FOXO3a and Its Regulators in Prostate Cancer.International journal of molecular sciences · 2021
    Review
  14. Article
  15. Review
  16. Review
  17. Anti-Inflammatory Action and Mechanisms of Resveratrol.Molecules (Basel, Switzerland) · 2021
    Review
  18. Article
  19. Emerging Roles of SIRT1 in Alcoholic Liver Disease.International journal of biological sciences · 2020
    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

4 authors at 2 institutions in 1 country.

Chao LiDepartment of Urology, Zhongnan Hospital of Wuhan University, No. 169 DongHu Road, WuChang District, Wuhan, 430000, Hubei, People's Republic of China.
Wan-Li HuDepartment of Urology, Zhongnan Hospital of Wuhan University, No. 169 DongHu Road, WuChang District, Wuhan, 430000, Hubei, People's Republic of China. huwanli_urology@163.com.
Meng-Xin LuDepartment of Urology, Zhongnan Hospital of Wuhan University, No. 169 DongHu Road, WuChang District, Wuhan, 430000, Hubei, People's Republic of China.
Guan-Fa XiaoDepartment of Urology, Zhongnan Hospital of Wuhan University, No. 169 DongHu Road, WuChang District, Wuhan, 430000, Hubei, People's Republic of China.
Wuhan University · CNZhongnan Hospital of Wuhan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundResveratrol is reported to inhibit the growth of prostate, which is characteristic of benign prostatic hyperplasia (BPH) condition. However, the mechanism remains unclear. This study aimed to identify the effects and probable mechanism of resveratrol on BPH.

methodsWe used the BPH epithelial cell line BPH-1 to investigate the effect of resveratrol. Cells were treated with various concentrations of resveratrol, and its effects on cells viability, apoptosis, ROS accumulation, and cell cycle were assessed. Western blot was used to examine activation of p38 MAPK and protein levels of FOXO3a, Bcl2, Bcl-XL, and caspase3. Cells were also co-treated with the p38 MAPK inhibitor SB203580 or ROS scavenger N-Acetyl-L-cysteine (NAC) to further investigate the mechanism.

resultsResveratrol treatment inhibited the growth of BPH-1 and increased apoptosis of cells. In addition, levels of phosphorylated p38 MAPK level was elevated and FOXO3a repression was observed. Concomitantly, ROS was accumulated. All of these resveratrol-mediated effects were suppressed by additional treatment with SB203580 or NAC. Resveratrol was also found to induce cell cycle arrest at S phase.

conclusionsResveratrol can activate p38 MAPK and repress FOXO3a, thereby causing repression of SOD2, catalase, and increase of ROS accumulation, leading to apoptosis in BPH-1 cells.

Indexed as

ApoptosisCell CycleCell Line, TumorForkhead Box Protein O3HumansMalep38 Mitogen-Activated Protein KinasesProstatic HyperplasiaReactive Oxygen SpeciesResveratrolSignal TransductionForkhead Box Protein O3FOXO3 protein, humanp38 Mitogen-Activated Protein KinasesReactive Oxygen SpeciesResveratrolApoptosisBenign prostatic hyperplasiaFOXO3ap38 MAPKReactive oxygen speciesResveratrol

Identifiers

PMID31464618
PMCPMC6714439
OpenAlexW2970095821

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.