Evidence map›Paper›PMID 36434592›Full record

ArticleBMC women's health2022

Pentamidine inhibits proliferation, migration and invasion in endometrial cancer via the PI3K/AKT signaling pathway.

Lin Lin, Yunan Gao, Xiaochen Hu, Jiabao Ouyang, Chunbo Liu

Open access · goldAbstract read
In one paragraph

Article in BMC women's health, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 29% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. TetronicPharmaceutics · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Copper homeostasis and cuproptosis in gynecological cancers.Frontiers in cell and developmental biology · 2024
    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

5 authors at 2 institutions in 1 country.

Lin LinDepartment of Nuclear Medicine, The First Affiliated Hospital of Harbin Medical University, Harbin City, 150001, Heilongjiang Province, People's Republic of China. linlyn1986@hrbmu.edu.cn.
Yunan GaoDepartment of Cardiology, The Fourth Affiliated Hospital of Harbin Medical University, Harbin City, 150001, Heilongjiang Province, People's Republic of China.
Xiaochen HuDepartment of Respiratory Medicine, The First Affiliated Hospital of Harbin Medical University, Harbin city, 150001, Heilongjiang Province, People's Republic of China.
Jiabao OuyangUltrasound Department, The First Affiliated Hospital of Harbin Medical University, Harbin city, 150001, Heilongjiang Province, People's Republic of China.
Chunbo LiuUltrasound Department, The First Affiliated Hospital of Harbin Medical University, Harbin city, 150001, Heilongjiang Province, People's Republic of China.
Harbin Medical University · CNFirst Affiliated Hospital of Harbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPentamidine has been reported to have many pharmacological effects including anti- protozoal, anti-inflammatory, and anti-tumor activities. The aim of this study is to investigate the potential therapeutic role of Pentamidine and molecular mechanisms of Pentamidine on PI3K/AKT signaling pathway underlying the anti-tumor properties in endometrial cancer.

methodsOur study was carried out in the central laboratory of Harbin Medical University from 2019 to 2021. Human endometrial cancer cell lines Ishikawa and HEC-1A were treated with Pentamidine. The proliferation ability of cells was investigated by MTS and colony formation assays. The cell cycle distribution was detected by flow cytometry. Cell migration and invasion were analyzed by using the wound healing assay and Transwell assay. Western blotting was performed to measure the levels of AKT, p-AKT, MMP-2, and MMP-9.

resultsOur results revealed that treatment of Pentamidine inhibited proliferation, migration and invasion of Ishikawa and HEC-1A endometrial cancer cells. Mechanistic investigation showed that Pentamidine inhibited PI3K/AKT signaling pathway and also reduced the expression of MMP-2 and MMP-9. In addition, co-treatment with PI3K kinase inhibitor LY294002 and Pentamidine leaded to increased repression of cell viability and the protein expression of p-AKT in Ishikawa cells.

conclusionsPentamidine suppresses PI3K/AKT signaling pathway, and inhibits proliferation, migration and invasion of EC cells. These findings suggested that Pentamidine might be a potential candidate for treating EC through PI3K/AKT pathway.

Indexed as

Endometrial NeoplasmsPhosphatidylinositol 3-KinasesCell ProliferationFemaleHumansMatrix Metalloproteinase 2Matrix Metalloproteinase 9PentamidineProto-Oncogene Proteins c-aktSignal TransductionMatrix Metalloproteinase 2Matrix Metalloproteinase 9PentamidinePhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktEndometrial cancerLY294002PentamidinePI3K/AKT pathway

Identifiers

PMID36434592
PMCPMC9700983
OpenAlexW4310052258

What OpenQuestion holds

Textmetadata
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.