Evidence map›Paper›PMID 36575321›Full record

ArticleMolecular biology reports2023

TLR3 stimulation improves the migratory potency of adipose-derived mesenchymal stem cells through the stress response pathway in the melanoma mouse model.

Fatemeh Eskandari, Samira Zolfaghari, Ayna Yazdanpanah, Rima Manafi Shabestari, Motahareh Rajabi Fomeshi, Peiman B Milan, Jafar Kiani, Mina Soufi Zomorrod, Majid Safa

Abstract read
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In one paragraph

Article in Molecular biology reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 38% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. Review
  3. 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

9 authors at 2 institutions in 1 country.

Fatemeh EskandariCellular and Molecular Research Centre, Iran University of Medical Sciences, Tehran, Iran.
Samira ZolfaghariCellular and Molecular Research Centre, Iran University of Medical Sciences, Tehran, Iran.
Ayna YazdanpanahCellular and Molecular Research Centre, Iran University of Medical Sciences, Tehran, Iran.
Rima Manafi ShabestariDepartment of Hematology and Blood Banking, Faculty of Allied Medicine, Iran University of Medical Sciences, Tehran, Iran.
Motahareh Rajabi FomeshiCellular and Molecular Research Centre, Iran University of Medical Sciences, Tehran, Iran.
Peiman B MilanCellular and Molecular Research Centre, Iran University of Medical Sciences, Tehran, Iran.
Jafar KianiOncopathology Research Center, Iran University of Medical Sciences, Tehran, Iran.
Mina Soufi ZomorrodApplied cell Sciences Department, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.
Majid SafaCellular and Molecular Research Centre, Iran University of Medical Sciences, Tehran, Iran. majidsafa@gmail.com.
Iran University of Medical Sciences · IRTarbiat Modares University · IR

Funding

Iran University of Medical Sciences 13206
6 · The paper itself

Abstract

backgroundMesenchymal stem cells (MSCs) are utilized as a carrier of anti-tumor agents in targeted anti-cancer therapy. Despite the improvements in this area, there are still some unsolved issues in determining the appropriate dose, method of administration and biodistribution of MSCs. The current study aimed to determine the influence of toll-like receptor 3 (TLR3) stimulation on the potential of MSCs migration to the neoplasm environment in the mouse melanoma model. METHODS AND

resultsAdipose-derived MSCs (ADMSCs) were isolated from the GFP

conclusionThis research identified that TLR3 activation might improve the migration via the stimulation of stress response in the cells and depending on the agonist concentration and time exposure, this activated pathway drives the migratory behavior of MSCs.

Indexed as

MelanomaMesenchymal Stem CellsAnimalsDisease Models, AnimalIntegrinsMiceMice, Inbred C57BLTissue DistributionToll-Like Receptor 3IntegrinsTLR3 protein, mouseToll-Like Receptor 3Adipose-derived mesenchymal stem cells (ADMSCs)Melanoma mouse modelStress responseToll-like receptor 3 (TLR3)Tumor tropism

Identifiers

PMID36575321
OpenAlexW4312212518

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.