Evidence map›Paper›PMID 32110802›Full record

ArticleBioscience reports2020

Schizandrin A exhibits potent anticancer activity in colorectal cancer cells by inhibiting heat shock factor 1.

Bing-Chen Chen, Shi-Liang Tu, Bo-An Zheng, Quan-Jin Dong, Zi-Ang Wan, Qiao-Qiong Dai

Open access · goldAbstract read
In one paragraph

Article in Bioscience reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. HSF1 Activation Mechanisms, Disease Roles, and Small Molecule Therapeutics.International journal of biological sciences · 2025
    Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Heat Shock Proteins and HSF1 in Cancer.Frontiers in oncology · 2022
    Review
  12. Article
  13. Article
  14. Article
  15. 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

6 authors at 1 institution in 1 country.

Bing-Chen ChenThe Surgical Department of Coloproctology, Zhejiang Provincial People's Hospital, Hangzhou 310014, Zhejiang Province, China.
Shi-Liang TuThe Surgical Department of Coloproctology, Zhejiang Provincial People's Hospital, Hangzhou 310014, Zhejiang Province, China.
Bo-An ZhengThe Surgical Department of Coloproctology, Zhejiang Provincial People's Hospital, Hangzhou 310014, Zhejiang Province, China.
Quan-Jin DongThe Surgical Department of Coloproctology, Zhejiang Provincial People's Hospital, Hangzhou 310014, Zhejiang Province, China.
Zi-Ang WanThe Surgical Department of Coloproctology, Zhejiang Provincial People's Hospital, Hangzhou 310014, Zhejiang Province, China.
Qiao-Qiong DaiThe Surgical Department of Coloproctology, Zhejiang Provincial People's Hospital, Hangzhou 310014, Zhejiang Province, China.
Zhejiang Provincial People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Heat shock factor 1 (HSF1) is a powerful multifaceted oncogenic modifier that plays a role in maintaining the protein balance of cancer cells under various stresses. In recent studies, there have been reports of increased expression of HSF1 in colorectal cancer (CRC) cells, and the depletion of the HSF1 gene knockdown has inhibited colon cancer growth both in vivo and in vitro. Therefore, HSF1 is a promising target for colon cancer treatment and chemoprevention. In the present study, we found that Schizandrin A (Sch A) significantly inhibited the growth of CRC cell lines by inducing cell cycle arrest, apoptosis and death. Through HSE luciferase reporter assay and quantitative PCR (qPCR), we identified Sch A as a novel HSF1 inhibitor. In addition, Sch A could effectively inhibit the induction of HSF1 target proteins such as heat-shock protein (HSP) 70 (HSP70) and HSP27, whether in heat shock or normal temperature culture. In the Surface Plasmon Resonance (SPR) experiment, Sch A showed moderate affinity with HSF1, further confirming that Sch A might be a direct HSF1 inhibitor. The molecular docking and molecular dynamic simulation results of HSF1/Sch A suggested that Sch A formed key hydrogen bond and hydrophobic interactions with HSF1, which may contribute to its potent HSF1 inhibition. These findings provide clues for the design of novel HSF1 inhibitors and drug candidates for colon cancer treatment.

Indexed as

ApoptosisCell CycleCell Line, TumorChinaColonic NeoplasmsColorectal NeoplasmsCyclooctanesDNA-Binding ProteinsHeat Shock Transcription FactorsHSP27 Heat-Shock ProteinsHSP70 Heat-Shock ProteinsHumansLignansMolecular Docking SimulationPolycyclic CompoundsTranscription FactorsCyclooctanesDNA-Binding ProteinsHeat Shock Transcription FactorsHSF1 protein, humanHSP27 Heat-Shock ProteinsHSP70 Heat-Shock ProteinsLignansPolycyclic Compoundsschizandrin ATranscription FactorsCRCHSF1molecular docking and molecular dynamic simulationSch A

Identifiers

PMID32110802
PMCPMC7069920
OpenAlexW3007618199

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.