Enhancement of the Therapeutic Capacity of Mesenchymal Stem Cells by Genetic Modification: A Systematic Review
BackgroundThe therapeutic capacity of mesenchymal stem cells (also known as mesenchymal stromal cells/MSCs) depends on their ability to respond to the need of the damaged tissue by secreting beneficial paracrine factors. MSCs can be genetically engineered to express certain beneficial factors. The a...
Main Authors: | , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2020-10-01
|
Series: | Frontiers in Cell and Developmental Biology |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fcell.2020.587776/full |
id |
doaj-e70e04a7afdf457db828ff3cf456b874 |
---|---|
record_format |
Article |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jeanne Adiwinata Pawitan Jeanne Adiwinata Pawitan Jeanne Adiwinata Pawitan Thuy Anh Bui Wildan Mubarok Radiana Dhewayani Antarianto Radiana Dhewayani Antarianto Retno Wahyu Nurhayati Retno Wahyu Nurhayati Ismail Hadisoebroto Dilogo Ismail Hadisoebroto Dilogo Ismail Hadisoebroto Dilogo Delvac Oceandy Delvac Oceandy |
spellingShingle |
Jeanne Adiwinata Pawitan Jeanne Adiwinata Pawitan Jeanne Adiwinata Pawitan Thuy Anh Bui Wildan Mubarok Radiana Dhewayani Antarianto Radiana Dhewayani Antarianto Retno Wahyu Nurhayati Retno Wahyu Nurhayati Ismail Hadisoebroto Dilogo Ismail Hadisoebroto Dilogo Ismail Hadisoebroto Dilogo Delvac Oceandy Delvac Oceandy Enhancement of the Therapeutic Capacity of Mesenchymal Stem Cells by Genetic Modification: A Systematic Review Frontiers in Cell and Developmental Biology engineered MSCs tumor cancer metastasis bone defect animal models |
author_facet |
Jeanne Adiwinata Pawitan Jeanne Adiwinata Pawitan Jeanne Adiwinata Pawitan Thuy Anh Bui Wildan Mubarok Radiana Dhewayani Antarianto Radiana Dhewayani Antarianto Retno Wahyu Nurhayati Retno Wahyu Nurhayati Ismail Hadisoebroto Dilogo Ismail Hadisoebroto Dilogo Ismail Hadisoebroto Dilogo Delvac Oceandy Delvac Oceandy |
author_sort |
Jeanne Adiwinata Pawitan |
title |
Enhancement of the Therapeutic Capacity of Mesenchymal Stem Cells by Genetic Modification: A Systematic Review |
title_short |
Enhancement of the Therapeutic Capacity of Mesenchymal Stem Cells by Genetic Modification: A Systematic Review |
title_full |
Enhancement of the Therapeutic Capacity of Mesenchymal Stem Cells by Genetic Modification: A Systematic Review |
title_fullStr |
Enhancement of the Therapeutic Capacity of Mesenchymal Stem Cells by Genetic Modification: A Systematic Review |
title_full_unstemmed |
Enhancement of the Therapeutic Capacity of Mesenchymal Stem Cells by Genetic Modification: A Systematic Review |
title_sort |
enhancement of the therapeutic capacity of mesenchymal stem cells by genetic modification: a systematic review |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Cell and Developmental Biology |
issn |
2296-634X |
publishDate |
2020-10-01 |
description |
BackgroundThe therapeutic capacity of mesenchymal stem cells (also known as mesenchymal stromal cells/MSCs) depends on their ability to respond to the need of the damaged tissue by secreting beneficial paracrine factors. MSCs can be genetically engineered to express certain beneficial factors. The aim of this systematic review is to compile and analyze published scientific literatures that report the use of engineered MSCs for the treatment of various diseases/conditions, to discuss the mechanisms of action, and to assess the efficacy of engineered MSC treatment.MethodsWe retrieved all published studies in PubMed/MEDLINE and Cochrane Library on July 27, 2019, without time restriction using the following keywords: “engineered MSC” and “therapy” or “manipulated MSC” and “therapy.” In addition, relevant articles that were found during full text search were added. We identified 85 articles that were reviewed in this paper.ResultsOf the 85 articles reviewed, 51 studies reported the use of engineered MSCs to treat tumor/cancer/malignancy/metastasis, whereas the other 34 studies tested engineered MSCs in treating non-tumor conditions. Most of the studies reported the use of MSCs in animal models, with only one study reporting a trial in human subjects. Thirty nine studies showed that the expression of beneficial paracrine factors would significantly enhance the therapeutic effects of the MSCs, whereas thirty three studies showed moderate effects, and one study in humans reported no effect. The mechanisms of action for MSC-based cancer treatment include the expression of “suicide genes,” induction of tumor cell apoptosis, and delivery of cytokines to induce an immune response against cancer cells. In the context of the treatment of non-cancerous diseases, the mechanism described in the reviewed papers included the expression of angiogenic, osteogenic, and growth factors.ConclusionThe therapeutic capacity of MSCs can be enhanced by inducing the expression of certain paracrine factors by genetic modification. Genetically engineered MSCs have been used successfully in various animal models of diseases. However, the results should be interpreted cautiously because animal models might not perfectly represent real human diseases. Therefore, further studies are needed to explore the translational potential of genetically engineered MSCs. |
topic |
engineered MSCs tumor cancer metastasis bone defect animal models |
url |
https://www.frontiersin.org/articles/10.3389/fcell.2020.587776/full |
work_keys_str_mv |
AT jeanneadiwinatapawitan enhancementofthetherapeuticcapacityofmesenchymalstemcellsbygeneticmodificationasystematicreview AT jeanneadiwinatapawitan enhancementofthetherapeuticcapacityofmesenchymalstemcellsbygeneticmodificationasystematicreview AT jeanneadiwinatapawitan enhancementofthetherapeuticcapacityofmesenchymalstemcellsbygeneticmodificationasystematicreview AT thuyanhbui enhancementofthetherapeuticcapacityofmesenchymalstemcellsbygeneticmodificationasystematicreview AT wildanmubarok enhancementofthetherapeuticcapacityofmesenchymalstemcellsbygeneticmodificationasystematicreview AT radianadhewayaniantarianto enhancementofthetherapeuticcapacityofmesenchymalstemcellsbygeneticmodificationasystematicreview AT radianadhewayaniantarianto enhancementofthetherapeuticcapacityofmesenchymalstemcellsbygeneticmodificationasystematicreview AT retnowahyunurhayati enhancementofthetherapeuticcapacityofmesenchymalstemcellsbygeneticmodificationasystematicreview AT retnowahyunurhayati enhancementofthetherapeuticcapacityofmesenchymalstemcellsbygeneticmodificationasystematicreview AT ismailhadisoebrotodilogo enhancementofthetherapeuticcapacityofmesenchymalstemcellsbygeneticmodificationasystematicreview AT ismailhadisoebrotodilogo enhancementofthetherapeuticcapacityofmesenchymalstemcellsbygeneticmodificationasystematicreview AT ismailhadisoebrotodilogo enhancementofthetherapeuticcapacityofmesenchymalstemcellsbygeneticmodificationasystematicreview AT delvacoceandy enhancementofthetherapeuticcapacityofmesenchymalstemcellsbygeneticmodificationasystematicreview AT delvacoceandy enhancementofthetherapeuticcapacityofmesenchymalstemcellsbygeneticmodificationasystematicreview |
_version_ |
1725044068352786432 |
spelling |
doaj-e70e04a7afdf457db828ff3cf456b8742020-11-25T01:40:42ZengFrontiers Media S.A.Frontiers in Cell and Developmental Biology2296-634X2020-10-01810.3389/fcell.2020.587776587776Enhancement of the Therapeutic Capacity of Mesenchymal Stem Cells by Genetic Modification: A Systematic ReviewJeanne Adiwinata Pawitan0Jeanne Adiwinata Pawitan1Jeanne Adiwinata Pawitan2Thuy Anh Bui3Wildan Mubarok4Radiana Dhewayani Antarianto5Radiana Dhewayani Antarianto6Retno Wahyu Nurhayati7Retno Wahyu Nurhayati8Ismail Hadisoebroto Dilogo9Ismail Hadisoebroto Dilogo10Ismail Hadisoebroto Dilogo11Delvac Oceandy12Delvac Oceandy13Department of Histology, Faculty of Medicine, Universitas Indonesia, Jakarta, IndonesiaStem Cell Medical Technology Integrated Service Unit, Dr. Cipto Mangunkusumo General Hospital, Faculty of Medicine, Universitas Indonesia, Jakarta, IndonesiaStem Cell and Tissue Engineering Research Center, Indonesia Medical Education and Research Institute, Faculty of Medicine, Universitas Indonesia, Jakarta, IndonesiaDivision of Cardiovascular Sciences, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, The University of Manchester, Manchester, United KingdomDivision of Chemical Engineering, Department of Materials Engineering Science, Graduate School of Engineering Science, Osaka University, Toyonaka, JapanDepartment of Histology, Faculty of Medicine, Universitas Indonesia, Jakarta, IndonesiaStem Cell and Tissue Engineering Research Center, Indonesia Medical Education and Research Institute, Faculty of Medicine, Universitas Indonesia, Jakarta, IndonesiaStem Cell and Tissue Engineering Research Center, Indonesia Medical Education and Research Institute, Faculty of Medicine, Universitas Indonesia, Jakarta, IndonesiaDepartment of Biochemistry and Molecular Biology, Faculty of Medicine, Universitas Indonesia, Jakarta, IndonesiaStem Cell Medical Technology Integrated Service Unit, Dr. Cipto Mangunkusumo General Hospital, Faculty of Medicine, Universitas Indonesia, Jakarta, IndonesiaStem Cell and Tissue Engineering Research Center, Indonesia Medical Education and Research Institute, Faculty of Medicine, Universitas Indonesia, Jakarta, IndonesiaDepartment of Orthopaedic and Traumatology, Dr. Cipto Mangunkusumo General Hospital, Faculty of Medicine, Universitas Indonesia, Jakarta, IndonesiaDivision of Cardiovascular Sciences, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, The University of Manchester, Manchester, United KingdomDepartment of Biomedical Science, Faculty of Medicine, Universitas Airlangga, Surabaya, IndonesiaBackgroundThe therapeutic capacity of mesenchymal stem cells (also known as mesenchymal stromal cells/MSCs) depends on their ability to respond to the need of the damaged tissue by secreting beneficial paracrine factors. MSCs can be genetically engineered to express certain beneficial factors. The aim of this systematic review is to compile and analyze published scientific literatures that report the use of engineered MSCs for the treatment of various diseases/conditions, to discuss the mechanisms of action, and to assess the efficacy of engineered MSC treatment.MethodsWe retrieved all published studies in PubMed/MEDLINE and Cochrane Library on July 27, 2019, without time restriction using the following keywords: “engineered MSC” and “therapy” or “manipulated MSC” and “therapy.” In addition, relevant articles that were found during full text search were added. We identified 85 articles that were reviewed in this paper.ResultsOf the 85 articles reviewed, 51 studies reported the use of engineered MSCs to treat tumor/cancer/malignancy/metastasis, whereas the other 34 studies tested engineered MSCs in treating non-tumor conditions. Most of the studies reported the use of MSCs in animal models, with only one study reporting a trial in human subjects. Thirty nine studies showed that the expression of beneficial paracrine factors would significantly enhance the therapeutic effects of the MSCs, whereas thirty three studies showed moderate effects, and one study in humans reported no effect. The mechanisms of action for MSC-based cancer treatment include the expression of “suicide genes,” induction of tumor cell apoptosis, and delivery of cytokines to induce an immune response against cancer cells. In the context of the treatment of non-cancerous diseases, the mechanism described in the reviewed papers included the expression of angiogenic, osteogenic, and growth factors.ConclusionThe therapeutic capacity of MSCs can be enhanced by inducing the expression of certain paracrine factors by genetic modification. Genetically engineered MSCs have been used successfully in various animal models of diseases. However, the results should be interpreted cautiously because animal models might not perfectly represent real human diseases. Therefore, further studies are needed to explore the translational potential of genetically engineered MSCs.https://www.frontiersin.org/articles/10.3389/fcell.2020.587776/fullengineered MSCstumorcancermetastasisbone defectanimal models |