Evidence map›Paper›PMID 31028200›Full record

ArticleIn vivo (Athens, Greece)

Fisetin Suppresses Human Osteosarcoma U-2 OS Cell Migration and Invasion

Jr-Kai Chen, Shu-Fen Peng, Kuang Chi Lai, Hsin-Chung Liu, Yi-Ping Huang, Chin-Chung Lin, An-Cheng Huang, Fu-Shin Chueh, Jing-Gung Chung

Open access · diamondAbstract read
In one paragraph

Article in In vivo (Athens, Greece). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.1field-weighted citation impact, top 15% 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

14 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  10. Implications of flavonoids as potential modulators of cancer neovascularity.Journal of cancer research and clinical oncology · 2020
    Review
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  12. Article
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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

9 authors at 3 institutions in 1 country.

Jr-Kai ChenAttending Physician of Orthopaedadics, Department of Chang Bing Show-Chwan Memorial Hospital, Changhua, Taiwan, R.O.C.
Shu-Fen PengDepartment of Biological Science and Technology, China Medical University, Taichung, Taiwan, R.O.C.
Kuang Chi LaiDepartment of Medical Laboratory Science and Biotechnology, College of Medicine and Life Science, Chung Hwa University of Medical Technology, Tainan, Taiwan, R.O.C.
Hsin-Chung LiuDepartment of Biological Science and Technology, China Medical University, Taichung, Taiwan, R.O.C.
Yi-Ping HuangDepartment of Physiology, College of Medicine, China Medical University, Taichung, Taiwan, R.O.C.
Chin-Chung LinDepartment of Chinese Medicine, Feng-Yuan Hospital, Ministry of Health and Welfare, Executive Yuan, Taichung, Taiwan, R.O.C.
An-Cheng HuangDepartment of Nursing, St. Mary's Junior College of Medicine, Nursing and Management, Yilan, Taiwan, R.O.C.
Fu-Shin Chueh *Department of Food Nutrition and Health Biotechnology, Asia University, Taichung, Taiwan, R.O.C. jgchung@mail.cmu.edu.tw fushin@asia.edu.tw.
Jing-Gung Chung *Department of Biological Science and Technology, China Medical University, Taichung, Taiwan, R.O.C. jgchung@mail.cmu.edu.tw fushin@asia.edu.tw.
Asia University · TWChina Medical University · TWTaichung Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimEvidence has indicated that fisetin induces cytotoxic effects in human cancer cell lines, including the inhibition of cell migration and invasion, however, the exact molecular mechanism of action of fisetin in human osteosarcoma cells remains unclear. MATERIALS AND

methodsThe anti-metastatic mechanisms of fisetin in human osteosarcoma U-2 OS cells were investigated in vitro.

resultsFisetin reduced the viability of cells at different concentrations (2.5, 5 and 10 μM) as measured by flow cytometric assay. Fisetin suppressed cell mobility, migration and invasion of U-2 OS cells, as shown by wound healing assay and transwell filter chambers, respectively. The gelatin zymography assay showed that fisetin inhibited MMP-2 activity in U-2 OS cells. Results from western blotting indicated that fisetin reduced the levels of pEGFR, SOS-1, GRB2, Ras, PKC, p-ERK1/2, p-JNK, p-p-38, VEGF, FAK, RhoA, PI3K, p-AKT, NF-ĸB, uPA, MMP-7, MMP-9, and MMP-13, but increased GSK3β and E-cadherin in U-2 OS cells after 48 h of treatment.

conclusionFisetin can be used in the future, as a target for the treatment of metastasis of human osteosarcoma cells.

Indexed as

Bone NeoplasmsCell Line, TumorCell MovementCell SurvivalFlavonoidsFlavonolsFocal Adhesion Kinase 1HumansModels, BiologicalNF-kappa BOsteosarcomaSignal TransductionUrokinase-Type Plasminogen ActivatorfisetinFlavonoidsFlavonolsFocal Adhesion Kinase 1NF-kappa BPTK2 protein, humanUrokinase-Type Plasminogen ActivatorFisetinhuman osteosarcoma U-2 OS cellinvasionmetastasismigration

Identifiers

PMID31028200
PMCPMC6559886
OpenAlexW2941508413

What OpenQuestion holds

Textmetadata
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.