Evidence map›Paper›PMID 36539682›Full record

ArticleHuman cell2023

Heterophyllin B inhibits the malignant phenotypes of gastric cancer cells via CXCR4.

Yunhai Wei, Lei Yin, Jinyu Zhang, Jianing Tang, Xiaofeng Yu, Zhongxin Wu, Yuhai Gao

Abstract read
PubMed Publisher
In one paragraph

Article in Human cell, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 32% 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

6 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Differences in Chemical Components and Antioxidant Ability Analysis ofInternational journal of molecular sciences · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Review
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 2 institutions in 1 country.

Yunhai WeiDepartment of Gastrointestinal Surgery, Huzhou Central Hospital, Affiliated Central Hospital Huzhou University, No.1558, Sanhuan North Road, Wuxing District, Huzhou, 313000, Zhejiang Province, China. weiyunhai1976@126.com.
Lei YinDepartment of Gastrointestinal Surgery, Huzhou Central Hospital, Affiliated Central Hospital Huzhou University, No.1558, Sanhuan North Road, Wuxing District, Huzhou, 313000, Zhejiang Province, China.
Jinyu ZhangDepartment of Gastrointestinal Surgery, Huzhou Central Hospital, Affiliated Central Hospital Huzhou University, No.1558, Sanhuan North Road, Wuxing District, Huzhou, 313000, Zhejiang Province, China.
Jianing TangDepartment of Gastrointestinal Surgery, Huzhou Central Hospital, Affiliated Central Hospital Huzhou University, No.1558, Sanhuan North Road, Wuxing District, Huzhou, 313000, Zhejiang Province, China.
Xiaofeng YuDepartment of General Surgery, Deqing Hospital of Traditional Chinese Medicine, Huzhou, 313299, Zhejiang Province, China.
Zhongxin WuDepartment of Gastrointestinal Surgery, Huzhou Central Hospital, Affiliated Central Hospital Huzhou University, No.1558, Sanhuan North Road, Wuxing District, Huzhou, 313000, Zhejiang Province, China.
Yuhai GaoDepartment of Gastrointestinal Surgery, Huzhou Central Hospital, Affiliated Central Hospital Huzhou University, No.1558, Sanhuan North Road, Wuxing District, Huzhou, 313000, Zhejiang Province, China.
Huzhou Central Hospital · CNHuzhou University · CN

Funding

Basic Public Welfare Research Program of Zhejiang Province LGF21H030002Huzhou Science and Technology Plan Project 2020GY53Huzhou Science and Technology Plan Project 2020GZ39Zhejiang Medical and Health Science and Technology Plan Project 2019ZD050
6 · The paper itself

Abstract

Heterophyllin B (HB) is a cyclic lipopeptide that has been shown to have anticancer effects. This study intended to further explore the effects and modulatory mechanism of HB in gastric cancer (GC) cells. The binding relationship between HB and CXCR4 was investigated by network pharmacological analysis, molecular docking, and cellular thermal shift assay (CETSA)-WB assay. Cellular assays revealed that HB could restrain GC cell viability, proliferation, invasion and migration by binding to CXCR4. Further studies presented that HB could suppress PI3K/AKT signaling pathway via binding to CXCR4, thus repressing PD-L1 expression. In vivo experiments in nude mice demonstrated that HB constrained PI3K/AKT signaling pathway to suppress GC cell metastasis and PD-L1 expression. In summary, the key target of HB in GC treatment was CXCR4. Cell experiments were employed for the investigation of the mechanism by which HB repressed GC cells. The results confirmed that HB could constrain the malignant progression of GC by the binding of HB into CXCR4 and suppressed PD-L1 expression via hampering PI3K/AKT signaling pathway.

Indexed as

Stomach NeoplasmsAnimalsB7-H1 AntigenCell Line, TumorCell MovementCell ProliferationGene Expression Regulation, NeoplasticMiceMice, NudeMolecular Docking SimulationPeptides, CyclicPhenotypePhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSignal TransductionB7-H1 Antigenheterophyllin BPeptides, CyclicPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktCXCR4Gastric cancerHeterophyllin BNetwork pharmacologyPD-L1

Identifiers

PMID36539682
OpenAlexW4312032772

What OpenQuestion holds

Textmetadata
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.