Evidence map›Paper›PMID 34725795›Full record

ArticleBreast cancer (Tokyo, Japan)2022

Effect of Apatinib plus melatonin on vasculogenic mimicry formation by cancer stem cells from breast cancer cell line.

Nazila Fathi Maroufi, Mohsen Rashidi, Vahid Vahedian, Raheleh Jahanbazi, Sahar Mostafaei, Maryam Akbarzadeh, Hamid Kazemzadeh, Hamid-Reza Nejabati, Alireza Isazadeh, Mohammad-Reza Rashidi and 1 more

Abstract read
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In one paragraph

Article in Breast cancer (Tokyo, Japan), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

12 citing papers in PubMed, 34 citations in OpenAlex.

  1. Effect ofCancer science · 2023
    Trial
  2. Review
  3. Article
  4. Melatonin and Breast Cancer: A Review Article.Chonnam medical journal · 2025
    Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. 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

11 authors at 5 institutions in 2 countries.

Nazila Fathi MaroufiStem Cell and Regenerative Medicine Institute, Tabriz University of Medical Sciences, Tabriz, Iran.
Mohsen RashidiDepartment of Pharmacology, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Vahid VahedianResearchers Club of Tums Preclinical Core Facility (TPCF), Tehran University of Medical Science (TUMS), Tehran, Iran.
Raheleh JahanbaziDepartment of Biology, Faculty of Science, Islamic Azad University, Falavarjan branch, Isfahan, Iran.
Sahar MostafaeiUrmia University of Medical Sciences, Urmia, Iran.
Maryam AkbarzadehDepartment of Biochemistry, Erasmus University Medical Center, Rotterdam, the Netherlands.
Hamid KazemzadehImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Hamid-Reza NejabatiDepartment of Biochemistry and Clinical Laboratories, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.
Alireza IsazadehImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Mohammad-Reza RashidiStem Cell and Regenerative Medicine Institute, Tabriz University of Medical Sciences, Tabriz, Iran. Rashidi@tbzmed.ac.ir.ORCID http://orcid.org/0000-0001-9206-9336
Mohammad NouriStem Cell and Regenerative Medicine Institute, Tabriz University of Medical Sciences, Tabriz, Iran. nourimd@yahoo.com.ORCID http://orcid.org/0000-0002-5367-9956
Tabriz University of Medical Sciences · IRErasmus MC · NLIslamic Azad University of Falavarjan · IRUniversity of Tehran · IRUrmia University · IR

Funding

tabriz university of medical sciences 59577
6 · The paper itself

Abstract

BACKGROUND AND

aimVasculogenic mimicry (VM) is one of the most important causes of breast cancer metastasis and resistance against drugs. The cancer stem cells (CSCs) are known as essential factors for VM formation. In this study, the effects of melatonin, Apatinib, and a combination of Apatinib/melatonin on VM formation were investigated by breast CSCs from breast cancer cell line. MATERIALS AND

methodsThe percentage of CSCs was determined in two breast cancer cell lines (MCF-7 and MDA-MB-231) by flow cytometry. The effects of Apatinib, melatonin, and a combination of Apatinib/melatonin were evaluated on proliferation and viability, migration and invasion, apoptosis, and VM formation in MDA-MB-231 cells. Moreover, expression levels of the involved proteins in cancer cell proliferation and viability, CSCs, migration and invasion, and VM formation were evaluated by real-time polymerase chain reaction (RT-PCR) and western blotting methods.

resultsResults of the present study showed that melatonin and Apatinib reduced survival rate of CSCs in a dose- and time-dependent manner. Apatinib, melatonin, and a combination of Apatinib/melatonin inhibited proliferation of breast CSCs (P ≤ 0.001). Formation of VM was decreased in the MDA-MB-231 cancer cell line treated with Apatinib and combination of Apatinib/melatonin. Apatinib and combination of Apatinib/melatonin reduced invasion of breast CSCs (P ≤ 0.0001). Expression of vascular endothelial VE-cadherin, ephrinA2 receptor (EPHA2), p-PI3K/phosphoinositide-3 kinase (PI3K) and phospho-AKT (p-AKT)/AKT ratios was decreased under the influence of Apatinib and a combination of Apatinib/melatonin (P ≤ 0.01).

conclusionApatinib or a combination of Apatinib/melatonin may be used to manage patients with breast cancer. However, further studies are needed to identify anti-cancer mechanisms of melatonin and Apatinib for better management of the patients with breast cancer.

Indexed as

Breast NeoplasmsMelatoninCell Line, TumorFemaleHumansMCF-7 CellsNeoplastic Stem CellsNeovascularization, PathologicPyridinesapatinibMelatoninPyridinesApatinibBreast cancerCancer stem cellsMelatoninVasculogenic mimicry

Identifiers

PMID34725795
OpenAlexW3211138231

What OpenQuestion holds

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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.