Evidence map›Paper›PMID 36831131›Full record

ArticleBiomedicines2023

Mesenchymal Stem Cells Genetically Modified by Lentivirus-Express Soluble TRAIL and Interleukin-12 Inhibit Growth and Reduced Metastasis-Relate Changes in Lymphoma Mice Model.

Adriana G Quiroz-Reyes, Carlos A Gonzalez-Villarreal, Alberto Y Limon-Flores, Paulina Delgado-Gonzalez, Herminia G Martinez-Rodriguez, Salvador L Said-Fernandez, Adolfo Soto-Dominguez, Ana M Rivas-Estilla, Jose F Islas, Juan F Molina-De la Garza and 1 more

Abstract read
In one paragraph

Article in Biomedicines, 2023. 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
–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

7 citing papers in PubMed.

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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

11 authors.

Adriana G Quiroz-ReyesDepartment of Biochemistry and Molecular Medicine, School of Medicine, Autonomous University of Nuevo Leon (UANL), Monterrey 64460, Mexico.
Carlos A Gonzalez-VillarrealDepartment of Basic Sciences, Laboratory of Molecular Genetics, University of Monterrey (UDEM), Monterrey 66238, Mexico.
Alberto Y Limon-FloresDepartment and Service of Immunology, School of Medicine, Autonomous University of Nuevo Leon (UANL), San Nicolás de los Garza 64460, Mexico.
Paulina Delgado-GonzalezDepartment of Biochemistry and Molecular Medicine, School of Medicine, Autonomous University of Nuevo Leon (UANL), Monterrey 64460, Mexico.
Herminia G Martinez-RodriguezDepartment of Biochemistry and Molecular Medicine, School of Medicine, Autonomous University of Nuevo Leon (UANL), Monterrey 64460, Mexico.
Salvador L Said-FernandezDepartment of Biochemistry and Molecular Medicine, School of Medicine, Autonomous University of Nuevo Leon (UANL), Monterrey 64460, Mexico.
Adolfo Soto-DominguezDepartment of Histology, School of Medicine, Autonomous University of Nuevo Leon (UANL), San Nicolás de los Garza 64460, Mexico.
Ana M Rivas-EstillaDepartment of Biochemistry and Molecular Medicine, School of Medicine, Autonomous University of Nuevo Leon (UANL), Monterrey 64460, Mexico.
Jose F IslasDepartment of Biochemistry and Molecular Medicine, School of Medicine, Autonomous University of Nuevo Leon (UANL), Monterrey 64460, Mexico.ORCID 0000-0002-0337-9912
Juan F Molina-De la GarzaDepartment of Biochemistry and Molecular Medicine, School of Medicine, Autonomous University of Nuevo Leon (UANL), Monterrey 64460, Mexico.ORCID 0000-0001-6287-0042
Elsa N Garza-TreviñoDepartment of Biochemistry and Molecular Medicine, School of Medicine, Autonomous University of Nuevo Leon (UANL), Monterrey 64460, Mexico.ORCID 0000-0002-1042-4603

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCancer treatment has many side effects; therefore, more efficient treatments are needed. Mesenchymal stem cells (MSC) have immunoregulatory properties, tumor site migration and can be genetically modified. Some proteins, such as soluble TRAIL (sTRAIL) and interleukin-12 (IL-12), have shown antitumoral potential, thus its combination in solid tumors could increase their activity. MATERIALS AND

methodsLentiviral transduction of bone marrow MSC with green fluorescent protein (GFP) and transgenes (sTRAIL and IL-12) was confirmed by fluorescence microscopy and Western blot. Soluble TRAIL levels were quantified by ELISA. Lymphoma L5178Y cells express a reporter gene (GFP/mCherry), and TRAIL receptor (DR5).

resultsAn in vivo model showed that combined treatment with MSC expressing sTRAIL+IL-12 or IL-12 alone significantly reduced tumor volume and increased survival in BALB/c mice (

conclusionsMSC expressing IL-12, is or combination with BM-MSC expressing sTRAIL represents an antitumor strategy for lymphoma tumors since they increase survival and reduce tumor development. However, the combination did not show significative additive effect. The localized application did not inhibit metastasis but reduced morphological alterations of tissue associated with liver metastasis.

Indexed as

interleulin-12 4lymphoma 2mesenchymal stem cells 1sTRAIL 5TNF-related apoptosis-inducing ligand 3

Identifiers

PMID36831131
PMCPMC9953195

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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.