Evidence map›Paper›PMID 35269887›Full record

ReviewInternational journal of molecular sciences2022

MSCs as Tumor-Specific Vectors for the Delivery of Anticancer Agents-A Potential Therapeutic Strategy in Cancer Diseases: Perspectives for Quinazoline Derivatives.

Monika Szewc, Elżbieta Radzikowska-Bűchner, Paulina Wdowiak, Joanna Kozak, Piotr Kuszta, Ewa Niezabitowska, Joanna Matysiak, Konrad Kubiński, Maciej Masłyk

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

15 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Frontiers in cell and developmental biology · 2025
    Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Design, synthesis,Heliyon · 2024
    Article
  12. Article
  13. Review
  14. Article
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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 at 4 institutions in 1 country.

Monika SzewcDepartment of Human Anatomy, Medical University of Lublin, 20-090 Lublin, Poland.
Elżbieta Radzikowska-BűchnerDepartment of Plastic, Reconstructive and Maxillary Surgery, Central Clinical Hospital MSWiA, 02-507 Warsaw, Poland.
Paulina WdowiakDepartment of Human Anatomy, Medical University of Lublin, 20-090 Lublin, Poland.ORCID 0000-0003-4007-7646
Joanna KozakDepartment of Human Anatomy, Medical University of Lublin, 20-090 Lublin, Poland.ORCID 0000-0002-2004-3732
Piotr KusztaDepartment of Human Anatomy, Medical University of Lublin, 20-090 Lublin, Poland.
Ewa NiezabitowskaDepartment of Urology and Urological Oncology, Multidisciplinary Hospital in Lublin, 20-400 Lublin, Poland.
Joanna MatysiakDepartment of Chemistry, University of Life Sciences in Lublin, 20-950 Lublin, Poland.ORCID 0000-0002-0363-4450
Konrad KubińskiDepartment of Molecular Biology, The John Paul II Catholic University of Lublin, 20-708 Lublin, Poland.ORCID 0000-0001-6870-845X
Maciej MasłykDepartment of Molecular Biology, The John Paul II Catholic University of Lublin, 20-708 Lublin, Poland.ORCID 0000-0003-0516-3231
Medical University of Lublin · PLJohn Paul II Catholic University of Lublin · PLCentral Clinical Hospital · PLUniversity of Life Sciences in Lublin · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal stem cells (MSCs) are considered to be a powerful tool in the treatment of various diseases. Scientists are particularly interested in the possibility of using MSCs in cancer therapy. The research carried out so far has shown that MSCs possess both potential pro-oncogenic and anti-oncogenic properties. It has been confirmed that MSCs can regulate tumor cell growth through a paracrine mechanism, and molecules secreted by MSCs can promote or block a variety of signaling pathways. These findings may be crucial in the development of new MSC-based cell therapeutic strategies. The abilities of MSCs such as tumor tropism, deep migration and immune evasion have evoked considerable interest in their use as tumor-specific vectors for small-molecule anticancer agents. Studies have shown that MSCs can be successfully loaded with chemotherapeutic drugs such as gemcitabine and paclitaxel, and can release them at the site of primary and metastatic neoplasms. The inhibitory effect of MSCs loaded with anti-cancer agents on the proliferation of cancer cells has also been observed. However, not all known chemotherapeutic agents can be used in this approach, mainly due to their cytotoxicity towards MSCs and insufficient loading and release capacity. Quinazoline derivatives appear to be an attractive choice for this therapeutic solution due to their biological and pharmacological properties. There are several quinazolines that have been approved for clinical use as anticancer drugs by the US Food and Drug Administration (FDA). It gives hope that the synthesis of new quinazoline derivatives and the development of methods of their application may contribute to the establishment of highly effective therapies for oncological patients. However, a deeper understanding of interactions between MSCs and tumor cells, and the exploration of the possibilities of using quinazoline derivatives in MSC-based therapy is necessary to achieve this goal. The aim of this review is to discuss the prospects for using MSC-based cell therapy in cancer treatment and the potential use of quinazolines in this procedure.

Indexed as

Antineoplastic AgentsMesenchymal Stem CellsNeoplasmsDrug Delivery SystemsHumansQuinazolinesAntineoplastic AgentsQuinazolinescancer treatmentmesenchymal stem cellsMSC-based cell therapyquinazoline derivatives

Identifiers

PMID35269887
PMCPMC8911180
OpenAlexW4214917277

What OpenQuestion holds

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LicenceCC BY
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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.