Evidence map›Paper›PMID 31438640›Full record

ArticleCells2019

Fisetin Suppresses the Proliferation and Metastasis of Renal Cell Carcinoma through Upregulation of MEK/ERK-Targeting CTSS and ADAM9.

Min-Hong Hsieh, Jen-Pi Tsai, Shun-Fa Yang, Hui-Ling Chiou, Chia-Liang Lin, Yi-Hsien Hsieh, Horng-Rong Chang

Open access · goldAbstract read
In one paragraph

Article in Cells, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 6% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

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  13. Pharmaceuticals (Basel, Switzerland) · 2022
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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

7 authors at 3 institutions in 1 country.

Min-Hong HsiehInstitute of Medicine, Chung Shan Medical University, Taichung 40201, Taiwan.
Jen-Pi TsaiSchool of Medicine, Tzu Chi University, Hualien 97071, Taiwan.
Shun-Fa YangInstitute of Medicine, Chung Shan Medical University, Taichung 40201, Taiwan.
Hui-Ling ChiouSchool of Medical Laboratory and Biotechnology, Chung Shan Medical University, Taichung 40201, Taiwan.
Chia-Liang LinDepartment of Biochemistry, School of Medicine, Chung Shan Medical University, Taichung 40201, Taiwan.
Yi-Hsien HsiehDepartment of Biochemistry, School of Medicine, Chung Shan Medical University, Taichung 40201, Taiwan. hyhsien@csmu.edu.tw.
Horng-Rong ChangInstitute of Medicine, Chung Shan Medical University, Taichung 40201, Taiwan. chr@csmu.edu.tw.
Chung Shan Medical University · TWChung Shan Medical University Hospital · TWTzu Chi University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fisetin, a natural flavonoid, is known to have anticarcinogenic effects against several cancers, but its role in mediating renal cell carcinoma (RCC) progression has not been delineated. Cell viability, cytotoxicity, and cell cycle distribution were measured using the 3-(4,5-cimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide assay and propidium iodide staining with flow cytometry. The in vitro migration and invasion assay was used to examine in vivo cell migration and invasion. Human protease antibody array analysis was conducted with cell migration/invasion-related proteins. Western blotting and quantitative reverse transcription polymerase chain reaction were used for assessing protein expression related to the cell cycle, cell invasion, and mitogen-activated protein kinase (MAPK) signaling pathway. We found that fisetin significantly inhibited cell viability through cell cycle arrest in the G2/M phase, in addition to downregulating cyclin D1 and upregulating p21/p27. Fisetin inhibited the migration and invasion of human RCC cells through the downregulation of CTSS and a disintegrin and metalloproteinase 9 (ADAM9). Fisetin also upregulated ERK phosphorylation in 786-O and Caki-1 cells. Furthermore, treatment with a MEK inhibitor (UO126) reduced the inhibitory effects of fisetin on the metastasis of RCC cells through the ERK/CTSS/ADAM9 pathway. Fisetin inhibits proliferation and metastasis of RCC cells by downregulating CTSS and ADAM9 through the MEK/ERK signaling pathway. These findings indicate that fisetin is a promising antitumor agent against RCC.

Indexed as

ADAM ProteinsAntineoplastic AgentsCarcinoma, Renal CellCathepsinsCell MovementCell ProliferationCell SurvivalDose-Response Relationship, DrugDrug Screening Assays, AntitumorFlavonoidsFlavonolsHumansKidney NeoplasmsMAP Kinase Signaling SystemMembrane ProteinsMolecular StructureADAM9 protein, humanADAM ProteinsAntineoplastic Agentscathepsin SCathepsinsfisetinFlavonoidsFlavonolsMembrane ProteinsADAM9CTSSfisetininvasionmigrationproliferationrenal cell carcinoma

Identifiers

PMID31438640
PMCPMC6770737
OpenAlexW2969347269

What OpenQuestion holds

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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.