Evidence map›Paper›PMID 34712379›Full record

ArticleOxidative medicine and cellular longevity2021

Berberine Suppresses EMT in Liver and Gastric Carcinoma Cells through Combination with TGF

Haiyan Du, Jiangyong Gu, Qin Peng, Xiaolan Wang, Lei Liu, Xuanyu Shu, Qiuying He, Yuhui Tan

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

28 citing papers in PubMed, 49 citations in OpenAlex.

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  8. A novel HVEM-Fc recombinant protein for lung cancer immunotherapy.Journal of experimental & clinical cancer research : CR · 2025
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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.

Haiyan DuDepartment of Biochemistry and Molecular Biology School of Basic Medical Sciences, Guangzhou University of Chinese Medicine, Guangzhou, 510006 Guangdong, China.
Jiangyong GuDepartment of Biochemistry and Molecular Biology School of Basic Medical Sciences, Guangzhou University of Chinese Medicine, Guangzhou, 510006 Guangdong, China.
Qin PengDepartment of Biochemistry and Molecular Biology School of Basic Medical Sciences, Guangzhou University of Chinese Medicine, Guangzhou, 510006 Guangdong, China.
Xiaolan WangDepartment of Biochemistry and Molecular Biology School of Basic Medical Sciences, Guangzhou University of Chinese Medicine, Guangzhou, 510006 Guangdong, China.
Lei LiuDepartment of Biochemistry and Molecular Biology School of Basic Medical Sciences, Guangzhou University of Chinese Medicine, Guangzhou, 510006 Guangdong, China.
Xuanyu ShuDepartment of Biochemistry and Molecular Biology School of Basic Medical Sciences, Guangzhou University of Chinese Medicine, Guangzhou, 510006 Guangdong, China.
Qiuying HeDepartment of Biochemistry and Molecular Biology School of Basic Medical Sciences, Guangzhou University of Chinese Medicine, Guangzhou, 510006 Guangdong, China.
Yuhui TanDepartment of Biochemistry and Molecular Biology School of Basic Medical Sciences, Guangzhou University of Chinese Medicine, Guangzhou, 510006 Guangdong, China.ORCID https://orcid.org/0000-0001-8203-0630
Guangzhou University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Berberine (BBR), a natural alkaloid derived from Coptis, has anticancer activity. Some researchers have found that it could restrain epithelial-mesenchymal transition (EMT) of melanoma, neuroblastoma, and other tumor cells. However, it is unclear whether BBR can reverse EMT in hepatocellular carcinoma (HCC) and gastric carcinoma (GC). In our study, BBR inhibited the migration and invasion of HepG2, MGC803, and SGC7901 cells in a dose-dependent manner. Transcription sequencing assays showed that Vimentin, MMP, and Smad3 were downregulated, but Smad2, Smad6, TAB2, ZO-1, and claudin 7 were upregulated when treated with BBR. GO Enrichment analysis of KEGG pathway showed that BBR significantly inhibited TGF-

Indexed as

Antineoplastic Agents, PhytogenicBerberineCell MovementCell ProliferationEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticHep G2 CellsHumansLiver NeoplasmsNeoplasm InvasivenessPhosphatidylinositol 3-KinasePhosphorylationProto-Oncogene Proteins c-aktReceptor, Transforming Growth Factor-beta Type IReceptor, Transforming Growth Factor-beta Type IISignal TransductionAntineoplastic Agents, PhytogenicBerberinePhosphatidylinositol 3-KinaseProto-Oncogene Proteins c-aktReceptor, Transforming Growth Factor-beta Type IReceptor, Transforming Growth Factor-beta Type IISmad2 ProteinSMAD2 protein, humanSmad3 ProteinSMAD3 protein, humanTGFBR1 protein, humanTGFBR2 protein, human

Identifiers

PMID34712379
PMCPMC8548148
OpenAlexW3205916516

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.