Evidence map›Paper›PMID 38797895›Full record

ReviewCurrent topics in medicinal chemistry2025

Revolutionizing Cancer Treatment: Harnessing the Power of Mesenchymal Stem Cells for Precise Targeted Therapy in the Tumor Microenvironment.

Shahram Taeb, Davoud Rostamzadeh, Seyed Mohammad Amini, Mohammad Rahmati, Mostafa Golshekan, Mahmoud Abedinzade, Elham Ahmadi, Singh Neha, Masoud Najafi

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current topics in medicinal chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
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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.

Shahram TaebDepartment of Radiology, School of Paramedical Sciences, Guilan University of Medical Sciences, Rasht, Iran.
Davoud RostamzadehDepartment of Immunology, University of Connecticut Health Center, Farmington, CT 06030, Connecticut, USA.
Seyed Mohammad AminiRadiation Biology Research center, Iran University of Medical Sciences, Tehran, Iran.
Mohammad RahmatiDepartment of Medical Biotechnology, Faculty of Paramedicine, Guilan University of Medical Sciences, Rasht, Iran.
Mostafa GolshekanGuilan Road Trauma Research Center, Guilan University of Medical Sciences, Rasht, Iran.
Mahmoud AbedinzadeDepartment of Medical Physiology, School of Medicine, Guilan University of Medical Sciences, Rasht, Iran.
Elham AhmadiDepartment of Immunology, University of Connecticut Health Center, Farmington, CT 06030, Connecticut, USA.
Singh NehaDepartment of Immunology, University of Connecticut Health Center, Farmington, CT 06030, Connecticut, USA.
Masoud NajafiMedical Technology Research Center, Institute of Health Technology, Kermanshah University of Medical Sciences, Kermanshah, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In recent years, mesenchymal stem cells (MSCs) have emerged as promising anti-- cancer mediators with the potential to treat several cancers. MSCs have been modified to produce anti-proliferative, pro-apoptotic, and anti-angiogenic molecules that could be effective against a variety of malignancies. Additionally, customizing MSCs with cytokines that stimulate pro-tumorigenic immunity or using them as vehicles for traditional chemical molecules with anti-cancer characteristics. Even though the specific function of MSCs in tumors is still challenged, promising outcomes from preclinical investigations of MSC-based gene therapy for a variety of cancers inspire the beginning of clinical trials. In addition, the tumor microenvironment (TME) could have a substantial influence on normal tissue stem cells, which can affect the treatment outcomes. To overcome the complications of TME in cancer development, MSCs could provide some signs of hope for converting TME into unequivocal therapeutic tools. Hence, this review focuses on engineered MSCs (En-MSCs) as a promising approach to overcoming the complications of TME.

Indexed as

Antineoplastic AgentsMesenchymal Stem CellsMesenchymal Stem Cell TransplantationNeoplasmsTumor MicroenvironmentAnimalsHumansAntineoplastic AgentsAngiogenesis.CancerCytokinesEngineered MSCs (En-MSCs)Mesenchymal stem cells (MSCs)Stem cellsTumor microenvironment (TME)

Identifiers

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.