Evidence map›Paper›PMID 39207449›Full record

ArticleAging2024

Treatment of tumor-associated macrophages with PD-1 monoclonal antibodies affects vascular generation in cervical cancer via the PD-1/IRE1α/SHP2/HIF1α signaling pathway.

Xiaohui Hao, Weiwei Zhao, Xianyu Zhang, Xiurong Lu, Cong Wang, Zhilin Zhang

Abstract read
In one paragraph

Article in Aging, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

6 authors.

Xiaohui HaoDepartment of Radiotherapy, The First Affiliated Hospital of Hebei North University, Zhangjiakou, Hebei, China.
Weiwei ZhaoDepartment of Radiotherapy, The First Affiliated Hospital of Hebei North University, Zhangjiakou, Hebei, China.
Xianyu ZhangDepartment of Radiotherapy, The First Affiliated Hospital of Hebei North University, Zhangjiakou, Hebei, China.
Xiurong LuDepartment of Radiotherapy, The First Affiliated Hospital of Hebei North University, Zhangjiakou, Hebei, China.
Cong WangDepartment of Radiotherapy, The First Affiliated Hospital of Hebei North University, Zhangjiakou, Hebei, China.
Zhilin ZhangDepartment of Radiotherapy, The First Affiliated Hospital of Hebei North University, Zhangjiakou, Hebei, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate the effect of PD-1 monoclonal antibodies in tumor-associated macrophages on angiogenesis in cervical cancer and its mechanism of action.

methodsThe effect of PD-1 monoclonal antibodies on the progression of cervical cancer was assessed using the nude mouse xenograft model and HE staining; the impact of PD-1 monoclonal antibodies on cervical cancer cell migration was evaluated using wound healing assay and Transwell assay; the effect on vascular formation in cervical cancer cells was examined using an angiogenesis assay; the impact on the expression of related proteins was tested using Western blotting.

resultsPD-1 monoclonal antibodies in tumor-associated macrophages can regulate and thus inhibit the progression of cervical cancer while promoting the expression of SHP2. Additionally, Sindilizumab inhibited the expression of tissue-type fibrinogen activator K and HIF1α through the PD-1/IRE1α/SHP2 signaling pathway, which inhibited the migration and neovascularization of cervical cancer cells.

conclusionsThis study discovered that PD-1 monoclonal antibodies in tumor-associated macrophages inhibit vascular generation inside cervical cancer by affecting the PD-1/IRE1α/SHP2/HIF1α signaling pathway, providing a new therapeutic target for the treatment of cervical cancer.

Indexed as

Hypoxia-Inducible Factor 1, alpha SubunitMice, NudeNeovascularization, PathologicProgrammed Cell Death 1 ReceptorSignal TransductionTumor-Associated MacrophagesUterine Cervical NeoplasmsAnimalsAntibodies, MonoclonalCell Line, TumorCell MovementFemaleHumansMiceProtein Tyrosine Phosphatase, Non-Receptor Type 11Xenograft Model Antitumor AssaysAntibodies, MonoclonalHypoxia-Inducible Factor 1, alpha SubunitProgrammed Cell Death 1 ReceptorProtein Tyrosine Phosphatase, Non-Receptor Type 11cervical cancerHIF1αIRE1αSHP2Sindilizumabtumor-associated macrophages

Identifiers

PMID39207449
PMCPMC11424572

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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.