Evidence map›Paper›PMID 41839532›Full record

ArticlePhytotherapy research : PTR2026

Epigallocatechin-3-Gallate Suppresses Glioma by Targeting Integrin αvβ3/FAK/ERK Signaling Axis and Matrix Metalloproteinases.

Rui Sun, Yonghan Pan, Ning Yang, Bing Kang, Hong Xiao, Xianglong Tang, Taiping Li, Mengjie Zhao

Abstract read
In one paragraph

Article in Phytotherapy research : PTR, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Rui SunNeuro-Psychiatric Institute, Nanjing Brain Hospital Affiliated to Nanjing Medical University, Nanjing, China.
Yonghan PanDepartment of Neurosurgery, Nanjing Brain Hospital Affiliated to Nanjing Medical University, Nanjing, China.
Ning YangDepartment of Traditional Chinese Medicine, Nanjing Brain Hospital Affiliated to Nanjing Medical University, Nanjing, China.
Bing KangDepartment of Traditional Chinese Medicine, Nanjing Brain Hospital Affiliated to Nanjing Medical University, Nanjing, China.
Hong XiaoNeuro-Psychiatric Institute, Nanjing Brain Hospital Affiliated to Nanjing Medical University, Nanjing, China.
Xianglong TangNeuro-Psychiatric Institute, Nanjing Brain Hospital Affiliated to Nanjing Medical University, Nanjing, China.
Taiping LiNeuro-Psychiatric Institute, Nanjing Brain Hospital Affiliated to Nanjing Medical University, Nanjing, China.ORCID https://orcid.org/0000-0001-8217-989X
Mengjie ZhaoNeuro-Psychiatric Institute, Nanjing Brain Hospital Affiliated to Nanjing Medical University, Nanjing, China.

Funding

Nanjing Health Science and Technology Development Special Fund Project YKK23141the National Natural Science Foundation of China 82403956the National Natural Science Foundation of China 82473394The Young Talent Training Project for Traditional Chinese Medicine of Nanjing ZYQ20070The Young Talent Training Project for Traditional Chinese Medicine of Nanjing ZYQ20071
6 · The paper itself

Abstract

Epigallocatechin-3-gallate (EGCG), the most abundant and biologically active catechin in green tea, has been widely reported to exhibit anti-cancer properties in various tumor types. However, its therapeutic potential and underlying mechanisms on glioma remain ambiguous. This study aimed to investigate the in vitro and in vivo effects of EGCG on glioma, with a specific focus on elucidating its molecular mechanisms, particularly the modulation of integrin-mediated signaling pathways and matrix metalloproteinases' (MMPs) expressions. The anti-proliferative effects of EGCG were evaluated in human glioma cell lines (U87, U251, and LN229) using CCK-8, EdU, and colony formation assays. Cell migration and invasion were assessed by wound healing and transwell assays, while apoptosis was analyzed via flow cytometry. The potential molecular mechanisms underlying the inhibitory effects of EGCG on integrin αvβ3/FAK/ERK signaling pathway and MMP-2/MMP-9 were explored by western blotting analyses. In vivo antitumor efficacy of EGCG was evaluated using an intracranial xenograft model in nude mice, with or without co-administration of temozolomide (TMZ). Toxicity was monitored through body weight changes and histopathological examination. EGCG inhibited cell proliferation with IC

Indexed as

Brain NeoplasmsCatechinGliomaIntegrin alphaVbeta3MAP Kinase Signaling SystemAnimalsApoptosisCell Line, TumorCell MovementCell ProliferationDacarbazineFocal Adhesion Kinase 1HumansMatrix Metalloproteinase 2Matrix Metalloproteinase 9MiceCatechinDacarbazineepigallocatechin gallateFocal Adhesion Kinase 1Integrin alphaVbeta3Matrix Metalloproteinase 2Matrix Metalloproteinase 9PTK2 protein, humanTemozolomideEGCGgliomaMMP‐2/9temozolomideαvβ3/FAK/ERK axis

Identifiers

PMID41839532
PMCPMC13254006

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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.