Evidence map›Paper›PMID 31894337›Full record

ArticleMolecular medicine reports2020

Phellinus gilvus‑derived protocatechualdehyde induces G0/G1 phase arrest and apoptosis in murine B16‑F10 cells.

Shi Zhong, Qinshen Jin, Taihen Yu, Jianxun Zhu, Yougui Li

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. EngineeredFrontiers in bioengineering and biotechnology · 2022
    Article
  8. Article
  9. Article
  10. Aqueous extracts ofOncology letters · 2021
    Article
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

5 authors at 2 institutions in 1 country.

Shi ZhongSericultural Research Institute, Zhejiang Academy of Agricultural Sciences, Hangzhou, Zhejiang 310021, P.R. China.
Qinshen JinNanxun District Agricultural Technology Extension Service Center, Huzhou, Zhejiang 313009, P.R. China.
Taihen YuDepartment of Radiology, Zhejiang Provincial People's Hospital, Affiliated People's Hospital of Hangzhou Medical College, Hangzhou, Zhejiang 310014, P.R. China.
Jianxun ZhuSericultural Research Institute, Zhejiang Academy of Agricultural Sciences, Hangzhou, Zhejiang 310021, P.R. China.
Yougui LiSericultural Research Institute, Zhejiang Academy of Agricultural Sciences, Hangzhou, Zhejiang 310021, P.R. China.
Sericultural Research Institute · CNHangzhou Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protocatechualdehyde (PCA) is considered to be the main phenolic component of Phellinus gilvus responsible for its anticancer properties. Previous studies have demonstrated that PCA can have an anticancer effect on multiple cancer types, but little is known about the effect of PCA on melanoma cells. The present study investigated the inhibitory abilities and potential anticancer mechanisms of PCA on B16‑F10 cells using MTT assay. Cell apoptosis and cell cycle were assessed by flow cytometry using Annexin V‑FITC and propidium iodide staining. Whole‑transcriptome analysis was used to investigate the effects of PCA on gene expression. PCA significantly decreased cell viability, induced cell cycle arrest at G0/G1 phase and promoted apoptosis of B16‑F10 cells, suggesting that PCA could have anticancer effects against melanoma cells. Whole‑transcriptome analysis indicated that PCA treatment upregulated genes involved in histone modification and decreased the transcription of genes involved in DNA repair and replication. Kyoto Encyclopedia of Genes and Genomes analysis showed that PCA treatment enhanced the complement and coagulation cascades, and the p53 signaling pathway. The present results indicated that PCA could act as an antitumor agent in melanoma cells, which may provide experimental support for the development of novel therapies to treat melanoma.

Indexed as

AnimalsApoptosisBasidiomycotaBenzaldehydesCatecholsCell Cycle CheckpointsCell Line, TumorCell ProliferationCell SurvivalComputational BiologyG1 PhaseGene Expression ProfilingHumansMelanoma, ExperimentalMiceResting Phase, Cell CycleBenzaldehydesCatecholsprotocatechualdehydeTP53 protein, humanTumor Suppressor Protein p53apoptosisB16-F10 cellsmelanomap53 signaling pathwayprotocatechualdehyde

Identifiers

PMID31894337
PMCPMC7002996
OpenAlexW2995623212

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.