Evidence map›Paper›PMID 32566617›Full record

ArticleAnnals of translational medicine2020

The anti-tumor effect of taxifolin on lung cancer via suppressing stemness and epithelial-mesenchymal transition

Ronghua Wang, Xianjun Zhu, Qing Wang, Xiaoqing Li, Enling Wang, Qianqian Zhao, Qianqian Wang, Hongmei Cao

Open access · diamondAbstract read
In one paragraph

Article in Annals of translational medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.4field-weighted citation impact, top 5% 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

30 citing papers in PubMed, 61 citations in OpenAlex.

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  13. In-vitro and ex-vivo antidiabetic, and antioxidant activities of Box-Behnken design optimizedSaudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2023
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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

8 authors at 1 institution in 1 country.

Ronghua WangDepartment of Cardiothoracic Surgery, People's Hospital of Zhangqiu, Jinan 250200, China.
Xianjun ZhuDepartment of Oncology, People's Hospital of Zhangqiu, Jinan 250200, China.
Qing WangDepartment of Radiology, People's Hospital of Zhangqiu, Jinan 250200, China.
Xiaoqing LiDepartment of Rehabilitation, People's Hospital of Zhangqiu, Jinan 250200, China.
Enling WangDepartment of Respiration, People's Hospital of Zhangqiu, Jinan 250200, China.
Qianqian ZhaoDepartment of Pharmacy Intravenous Admixture Services, People's Hospital of Zhangqiu, Jinan 250200, China.
Qianqian WangDepartment of Pharmacy Intravenous Admixture Services, People's Hospital of Zhangqiu, Jinan 250200, China.
Hongmei CaoDepartment of Out-patient, People's Hospital of Zhangqiu, Jinan 250200, China.
Zhangqiu City People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTaxifolin is a natural flavonoid with anti-oxidant and anti-proliferative properties. In this study, we investigated the stemness-related inhibitory effects of taxifolin in two lung cancer cell lines, A549 and H1975, as well as in A549 xenografts.

methodsA549 and H1975 cells, as well as A549 xenograft BALB/c mice were treated with taxifolin. Cell viability, stemness, mobility and protein expression were tested with Cell counting kit-8 (CCK-8), Colony formation assay, Flow cytometry, Transwell, Western blot and Immunohistochemistry, respectively.

resultsCCK-8 exhibited an obvious toxicity of taxifolin to both cell lines at higher dose. Then taxifolin of 0, 25, 50, and 100 µM/L were subsequently used. Taxifolin exhibited inhibitory effects on stemness and sphere formation, reduced protein expression of SOX2 and OCT4, and reduced CD133-positive cells. Furthermore, taxifolin decreased invasive cells, reduced N-cadherin and vimentin while increased E-cadherin expression, indicating that epithelial-mesenchymal transition (EMT) was inhibited. All of the effects observed were exhibited in a dose-dependent manner, and A549 cells proved to be more sensitive to taxifolin than H1975 cells. Taxifolin inactivated PI3K and TCF4 protein phosphorylation; however, taxifolin was not observed to have an effect on NF-κB P65 or STAT3. Taxifolin also suppressed tumor growth in A549 xenograft BALB/c mice, with decreased SOX2 and OCT4 expression and inhibited PI3K and TCF4.

conclusionsIn summary, taxifolin inhibited stemness and EMT in lung cancer cells possibly via the inactivation of PI3K and OCT4. Taxifolin could be a potential prodrug or serve as an adjuvant in lung cancer treatment.

Indexed as

epithelial-mesenchymal transition (EMT)non-small cell lung cancer (NSCLC)stem-like propertyTaxifolin

Identifiers

PMID32566617
PMCPMC7290558
OpenAlexW3024240367

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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.