Evidence map›Paper›PMID 32409692›Full record

ArticleScientific reports2020

Fisetin induces apoptosis in uterine leiomyomas through multiple pathways.

Jin-Woo Lee, Hyuck Jai Choi, Eun-Jin Kim, Woo Yeon Hwang, Min-Hyung Jung, Kyung Sook Kim

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 17% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Pharmacological Approaches to Decelerate Aging: A Promising Path.Oxidative medicine and cellular longevity · 2022
    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

6 authors at 2 institutions in 1 country.

Jin-Woo LeeMedical Science Research Institute, Kyung Hee University Medical Center, Seoul, 02447, Korea.
Hyuck Jai ChoiEast-West Medical Research Institute, Kyung Hee University Medical Center, Seoul, 02447, Korea.
Eun-Jin KimEast-West Medical Research Institute, Kyung Hee University Medical Center, Seoul, 02447, Korea.
Woo Yeon HwangDepartment of Obstetrics & Gynecology, School of Medicine, Kyung Hee University, Kyung Hee University Medical Center, Seoul, 02447, Korea.
Min-Hyung Jung *Department of Obstetrics & Gynecology, School of Medicine, Kyung Hee University, Kyung Hee University Medical Center, Seoul, 02447, Korea. webhospital@naver.com.ORCID http://orcid.org/0000-0002-1263-8533
Kyung Sook Kim *Department of Biomedical Engineering, College of Medicine, Kyung Hee University, Seoul, 02447, Korea. moosou94@khu.ac.kr.
Kyung Hee University Medical Center · KRKyung Hee University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although uterine leiomyomas are the most common benign uterine tumors in women, there is no effective therapy that can also preserve the uterus and maintain fertility. The work aimed to work was to discover a potential natural agent that has pharmacological activities on uterine leiomyomas with fewer adverse effects. We chose Rhus verniciflua Stokes (RVS) as a candidate after primary cytotoxicity testing, and analyzed the RVS components that showed pharmacological activity. Leiomyoma cells and myometrium cells were cultured from uterine tissues obtained from patients, and were treated with RVS at varying concentrations. RVS was cytotoxic in both leiomyoma and myometrium cells; however, the effects were more prominent in the leiomyoma cells. Among the bioactive components of RVS, fisetin showed significant pharmacological effects on leiomyoma cells. Fisetin showed excellent leiomyoma cell cytotoxicity and induced apoptotic cell death with cell cycle arrest. The apoptotic cell death appeared to involve not one specific pathway but multichannel pathways (intrinsic, extrinsic, MARK, and p53-mediated pathways), and autophagy. The multichannel apoptosis pathways were activated with a low concentration of fisetin (<IC

Indexed as

ApoptosisAutophagic Cell DeathBiological ProductsCell SurvivalFlavonoidsFlavonolsHumansLeiomyomaModels, BiologicalSignal TransductionBiological ProductsfisetinFlavonoidsFlavonols

Identifiers

PMID32409692
PMCPMC7224361
OpenAlexW3024223854

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.