Evidence map›Paper›PMID 39549017›Full record

ArticleThe Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology2024

Scleromitrion diffusum (Willd.) R. J. Wang Inhibits Gastric Cancer via ERBB2/ERBB3/PI3K/AKT Pathway.

Wei Ye, Qiu Zhao, Peng Li, Tong Zhou

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Article in The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Wei YeDepartment of Oncology, Changzhou Cancer Hospital, Changzhou, China.
Qiu ZhaoDepartment of Oncology, Changzhou Cancer Hospital, Changzhou, China.
Peng LiDepartment of Oncology, Changzhou Cancer Hospital, Changzhou, China.
Tong ZhouDepartment of Oncology, Changzhou Cancer Hospital, Changzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/Aims: This study aimed to evaluate the anticarcinogenic potential of Scleromitrion diffusum (Willd.) R. J. Wang (SD) extracts in vitro, along with exploring the underlying compatibility mechanisms. Materials and Methods: Scleromitrion diffusum (Willd.) R. J. Wang extract was prepared and gastric cancer (GC) cells were treated to detect the half maximal inhibitory concentration (IC50)/proliferation and migration/invasion by MTS method and transwell assay. The compatibility mechanisms of SD were analyzed by systems pharmacology strategy, combined with cellular experimental validation. Results: Scleromitrion diffusum (Willd.) R. J. Wang extract showed inhibitory ability on the proliferation of the GC cell lines dose- and time-dependently. A total of 3 active ingredients are involved in anti-gastric cancer effects of SD, based on the top 50 pathways. The "herb-composition-target-pathway" network showed the multi-target and multi-pathway characteristics of SD. There were 52 related targets shared by SD and GC. The cellular experiments supported that SD significantly reduced ERBB2 and ERBB3 expression levels in GC cells. The overexpression of ERBB2 or ERBB3 partially offset the anti-tumor effects of SD. Conclusion: Scleromitrion diffusum (Willd.) R. J. Wang inhibited gastric cancer growth and metastasis in vitro, which may be related to the inhibition of the ERBB2/ERBB3/PI3K/AKT pathway.

Indexed as

Cell ProliferationErb-b2 Receptor Tyrosine KinasesPhosphatidylinositol 3-KinasesPlant ExtractsProto-Oncogene Proteins c-aktReceptor, ErbB-3Signal TransductionStomach NeoplasmsAntineoplastic Agents, PhytogenicCell Line, TumorCell MovementHumansAntineoplastic Agents, PhytogenicERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesERBB3 protein, humanPhosphatidylinositol 3-KinasesPlant ExtractsProto-Oncogene Proteins c-aktReceptor, ErbB-3antitumorgastric cancernetwork pharmacologyPI3K/AKT pathwayScleromitrion diffusum (Willd.) R. J. Wang

Identifiers

PMID39549017
PMCPMC11562600

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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.