Engineered Mesenchymal Stem Cells as Treatment for Cancers: Opportunities, Clinical Applications and Challenges

The insufficient and unspecific target of classical chemotherapies often leads to therapy resistance and cancer recurrence. Over the past decades, discoveries about mesenchymal stem cell (MSC) biology have provided new potential approaches to improve cancer therapy. Researchers have utilised the mul...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The Malaysian journal of medical sciences 2024-10, Vol.31 (5), p.56-82
Hauptverfasser: Shamsul Kamal, Aishah Amirah, Fakiruddin, Kamal Shaik, Bobbo, Khadijat Abubakar, Ling, King Hwa, Vidyadaran, Sharmili, Abdullah, Syahril
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 82
container_issue 5
container_start_page 56
container_title The Malaysian journal of medical sciences
container_volume 31
creator Shamsul Kamal, Aishah Amirah
Fakiruddin, Kamal Shaik
Bobbo, Khadijat Abubakar
Ling, King Hwa
Vidyadaran, Sharmili
Abdullah, Syahril
description The insufficient and unspecific target of classical chemotherapies often leads to therapy resistance and cancer recurrence. Over the past decades, discoveries about mesenchymal stem cell (MSC) biology have provided new potential approaches to improve cancer therapy. Researchers have utilised the multipotent, regenerative and immunosuppressive qualities of MSCs and tropisms towards inflammatory, hypoxic and malignant sites in various therapeutic applications. Although MSC-based therapies have generally been demonstrated safe, their effectiveness remains limited when these cells are used alone. However, through genetic engineering, researchers have proven that MSCs can be modified to have specialised delivery roles to increase their therapeutic efficacy in cancer treatment. They can be made to overexpress therapeutic proteins through viral or non-viral genetic modification, which enhances their innate properties. Nevertheless, these engineering strategies must be optimised to increase therapeutic efficacy and targeting effectiveness while minimising any loss of MSC function. This review underscores the cutting-edge methods for engineering MSCs, discusses their promise and the difficulties in translating them into clinical settings, and offers some prospective suggestions for the future on achieving their full therapeutic potential.
doi_str_mv 10.21315/mjms2024.31.5.5
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_11477465</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3117620136</sourcerecordid><originalsourceid>FETCH-LOGICAL-c280t-b6131999b70fd93fa4ae175abfcbfa9d2e78440575f0591668e95014a757585d3</originalsourceid><addsrcrecordid>eNpVUU1P3DAQtVAr2ELvnJCPPZDFn3HMpUIR_ZCoOECl3iwnmewaOXaws0j8e9zyoXKa0cy8N2_mIXRMyZpRTuXZdDdlRphYc7qWa7mHVow2pBKc8A9oRbkWFdXyzwH6lPMdIVyyutlHB6VOa8XZCsXLsHEBIMGAf0GG0G8fJ-vxzQITbsH7jG3GtwnsMkFY8BgTbm3oIeVzfD3PMS274BYH-RS33gXXF_DFPPuSLC6GAg8DbrfWewgbyEfo42h9hs8v8RD9_nZ52_6orq6__2wvrqqeNWSpurqcp7XuFBkHzUcrLFAlbTf23Wj1wEA1QhCp5EikpnXdgJaECqtKqZEDP0Rfn3nnXTfB0BftyXozJzfZ9GiideZ9J7it2cQHQ6lQStSyMHx5YUjxfgd5MZPLffmIDRB32XBKVc0I5XUZJc-jfYo5Jxjf9lBi_hllXo0qMCPNX_aT__W9AV6d4U_GzJGE</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3117620136</pqid></control><display><type>article</type><title>Engineered Mesenchymal Stem Cells as Treatment for Cancers: Opportunities, Clinical Applications and Challenges</title><source>DOAJ Directory of Open Access Journals</source><source>Bioline International</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>Shamsul Kamal, Aishah Amirah ; Fakiruddin, Kamal Shaik ; Bobbo, Khadijat Abubakar ; Ling, King Hwa ; Vidyadaran, Sharmili ; Abdullah, Syahril</creator><creatorcontrib>Shamsul Kamal, Aishah Amirah ; Fakiruddin, Kamal Shaik ; Bobbo, Khadijat Abubakar ; Ling, King Hwa ; Vidyadaran, Sharmili ; Abdullah, Syahril ; Haematology Unit, Cancer Research Centre, Institute for Medical Research, National Institutes of Health, Ministry of Health Malaysia, Selangor, Malaysia ; Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Selangor, Malaysia ; Malaysia Genome and Vaccine Institute, National Institutes of Biotechnology Malaysia, Selangor, Malaysia ; UPM-MAKNA Cancer Research Laboratory, Institute of Bioscience, Universiti Putra Malaysia, Selangor, Malaysia ; Department of Pathology, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Selangor, Malaysia ; Malaysian Research Institute on Ageing, Universiti Putra Malaysia, Selangor, Malaysia</creatorcontrib><description>The insufficient and unspecific target of classical chemotherapies often leads to therapy resistance and cancer recurrence. Over the past decades, discoveries about mesenchymal stem cell (MSC) biology have provided new potential approaches to improve cancer therapy. Researchers have utilised the multipotent, regenerative and immunosuppressive qualities of MSCs and tropisms towards inflammatory, hypoxic and malignant sites in various therapeutic applications. Although MSC-based therapies have generally been demonstrated safe, their effectiveness remains limited when these cells are used alone. However, through genetic engineering, researchers have proven that MSCs can be modified to have specialised delivery roles to increase their therapeutic efficacy in cancer treatment. They can be made to overexpress therapeutic proteins through viral or non-viral genetic modification, which enhances their innate properties. Nevertheless, these engineering strategies must be optimised to increase therapeutic efficacy and targeting effectiveness while minimising any loss of MSC function. This review underscores the cutting-edge methods for engineering MSCs, discusses their promise and the difficulties in translating them into clinical settings, and offers some prospective suggestions for the future on achieving their full therapeutic potential.</description><identifier>ISSN: 1394-195X</identifier><identifier>EISSN: 2180-4303</identifier><identifier>DOI: 10.21315/mjms2024.31.5.5</identifier><identifier>PMID: 39416732</identifier><language>eng</language><publisher>Malaysia: Penerbit Universiti Sains Malaysia</publisher><subject>Review</subject><ispartof>The Malaysian journal of medical sciences, 2024-10, Vol.31 (5), p.56-82</ispartof><rights>Penerbit Universiti Sains Malaysia, 2024.</rights><rights>Penerbit Universiti Sains Malaysia, 2024 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11477465/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11477465/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39416732$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shamsul Kamal, Aishah Amirah</creatorcontrib><creatorcontrib>Fakiruddin, Kamal Shaik</creatorcontrib><creatorcontrib>Bobbo, Khadijat Abubakar</creatorcontrib><creatorcontrib>Ling, King Hwa</creatorcontrib><creatorcontrib>Vidyadaran, Sharmili</creatorcontrib><creatorcontrib>Abdullah, Syahril</creatorcontrib><creatorcontrib>Haematology Unit, Cancer Research Centre, Institute for Medical Research, National Institutes of Health, Ministry of Health Malaysia, Selangor, Malaysia</creatorcontrib><creatorcontrib>Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Selangor, Malaysia</creatorcontrib><creatorcontrib>Malaysia Genome and Vaccine Institute, National Institutes of Biotechnology Malaysia, Selangor, Malaysia</creatorcontrib><creatorcontrib>UPM-MAKNA Cancer Research Laboratory, Institute of Bioscience, Universiti Putra Malaysia, Selangor, Malaysia</creatorcontrib><creatorcontrib>Department of Pathology, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Selangor, Malaysia</creatorcontrib><creatorcontrib>Malaysian Research Institute on Ageing, Universiti Putra Malaysia, Selangor, Malaysia</creatorcontrib><title>Engineered Mesenchymal Stem Cells as Treatment for Cancers: Opportunities, Clinical Applications and Challenges</title><title>The Malaysian journal of medical sciences</title><addtitle>Malays J Med Sci</addtitle><description>The insufficient and unspecific target of classical chemotherapies often leads to therapy resistance and cancer recurrence. Over the past decades, discoveries about mesenchymal stem cell (MSC) biology have provided new potential approaches to improve cancer therapy. Researchers have utilised the multipotent, regenerative and immunosuppressive qualities of MSCs and tropisms towards inflammatory, hypoxic and malignant sites in various therapeutic applications. Although MSC-based therapies have generally been demonstrated safe, their effectiveness remains limited when these cells are used alone. However, through genetic engineering, researchers have proven that MSCs can be modified to have specialised delivery roles to increase their therapeutic efficacy in cancer treatment. They can be made to overexpress therapeutic proteins through viral or non-viral genetic modification, which enhances their innate properties. Nevertheless, these engineering strategies must be optimised to increase therapeutic efficacy and targeting effectiveness while minimising any loss of MSC function. This review underscores the cutting-edge methods for engineering MSCs, discusses their promise and the difficulties in translating them into clinical settings, and offers some prospective suggestions for the future on achieving their full therapeutic potential.</description><subject>Review</subject><issn>1394-195X</issn><issn>2180-4303</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNpVUU1P3DAQtVAr2ELvnJCPPZDFn3HMpUIR_ZCoOECl3iwnmewaOXaws0j8e9zyoXKa0cy8N2_mIXRMyZpRTuXZdDdlRphYc7qWa7mHVow2pBKc8A9oRbkWFdXyzwH6lPMdIVyyutlHB6VOa8XZCsXLsHEBIMGAf0GG0G8fJ-vxzQITbsH7jG3GtwnsMkFY8BgTbm3oIeVzfD3PMS274BYH-RS33gXXF_DFPPuSLC6GAg8DbrfWewgbyEfo42h9hs8v8RD9_nZ52_6orq6__2wvrqqeNWSpurqcp7XuFBkHzUcrLFAlbTf23Wj1wEA1QhCp5EikpnXdgJaECqtKqZEDP0Rfn3nnXTfB0BftyXozJzfZ9GiideZ9J7it2cQHQ6lQStSyMHx5YUjxfgd5MZPLffmIDRB32XBKVc0I5XUZJc-jfYo5Jxjf9lBi_hllXo0qMCPNX_aT__W9AV6d4U_GzJGE</recordid><startdate>20241001</startdate><enddate>20241001</enddate><creator>Shamsul Kamal, Aishah Amirah</creator><creator>Fakiruddin, Kamal Shaik</creator><creator>Bobbo, Khadijat Abubakar</creator><creator>Ling, King Hwa</creator><creator>Vidyadaran, Sharmili</creator><creator>Abdullah, Syahril</creator><general>Penerbit Universiti Sains Malaysia</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20241001</creationdate><title>Engineered Mesenchymal Stem Cells as Treatment for Cancers: Opportunities, Clinical Applications and Challenges</title><author>Shamsul Kamal, Aishah Amirah ; Fakiruddin, Kamal Shaik ; Bobbo, Khadijat Abubakar ; Ling, King Hwa ; Vidyadaran, Sharmili ; Abdullah, Syahril</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c280t-b6131999b70fd93fa4ae175abfcbfa9d2e78440575f0591668e95014a757585d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Review</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shamsul Kamal, Aishah Amirah</creatorcontrib><creatorcontrib>Fakiruddin, Kamal Shaik</creatorcontrib><creatorcontrib>Bobbo, Khadijat Abubakar</creatorcontrib><creatorcontrib>Ling, King Hwa</creatorcontrib><creatorcontrib>Vidyadaran, Sharmili</creatorcontrib><creatorcontrib>Abdullah, Syahril</creatorcontrib><creatorcontrib>Haematology Unit, Cancer Research Centre, Institute for Medical Research, National Institutes of Health, Ministry of Health Malaysia, Selangor, Malaysia</creatorcontrib><creatorcontrib>Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Selangor, Malaysia</creatorcontrib><creatorcontrib>Malaysia Genome and Vaccine Institute, National Institutes of Biotechnology Malaysia, Selangor, Malaysia</creatorcontrib><creatorcontrib>UPM-MAKNA Cancer Research Laboratory, Institute of Bioscience, Universiti Putra Malaysia, Selangor, Malaysia</creatorcontrib><creatorcontrib>Department of Pathology, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Selangor, Malaysia</creatorcontrib><creatorcontrib>Malaysian Research Institute on Ageing, Universiti Putra Malaysia, Selangor, Malaysia</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Malaysian journal of medical sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shamsul Kamal, Aishah Amirah</au><au>Fakiruddin, Kamal Shaik</au><au>Bobbo, Khadijat Abubakar</au><au>Ling, King Hwa</au><au>Vidyadaran, Sharmili</au><au>Abdullah, Syahril</au><aucorp>Haematology Unit, Cancer Research Centre, Institute for Medical Research, National Institutes of Health, Ministry of Health Malaysia, Selangor, Malaysia</aucorp><aucorp>Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Selangor, Malaysia</aucorp><aucorp>Malaysia Genome and Vaccine Institute, National Institutes of Biotechnology Malaysia, Selangor, Malaysia</aucorp><aucorp>UPM-MAKNA Cancer Research Laboratory, Institute of Bioscience, Universiti Putra Malaysia, Selangor, Malaysia</aucorp><aucorp>Department of Pathology, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Selangor, Malaysia</aucorp><aucorp>Malaysian Research Institute on Ageing, Universiti Putra Malaysia, Selangor, Malaysia</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Engineered Mesenchymal Stem Cells as Treatment for Cancers: Opportunities, Clinical Applications and Challenges</atitle><jtitle>The Malaysian journal of medical sciences</jtitle><addtitle>Malays J Med Sci</addtitle><date>2024-10-01</date><risdate>2024</risdate><volume>31</volume><issue>5</issue><spage>56</spage><epage>82</epage><pages>56-82</pages><issn>1394-195X</issn><eissn>2180-4303</eissn><abstract>The insufficient and unspecific target of classical chemotherapies often leads to therapy resistance and cancer recurrence. Over the past decades, discoveries about mesenchymal stem cell (MSC) biology have provided new potential approaches to improve cancer therapy. Researchers have utilised the multipotent, regenerative and immunosuppressive qualities of MSCs and tropisms towards inflammatory, hypoxic and malignant sites in various therapeutic applications. Although MSC-based therapies have generally been demonstrated safe, their effectiveness remains limited when these cells are used alone. However, through genetic engineering, researchers have proven that MSCs can be modified to have specialised delivery roles to increase their therapeutic efficacy in cancer treatment. They can be made to overexpress therapeutic proteins through viral or non-viral genetic modification, which enhances their innate properties. Nevertheless, these engineering strategies must be optimised to increase therapeutic efficacy and targeting effectiveness while minimising any loss of MSC function. This review underscores the cutting-edge methods for engineering MSCs, discusses their promise and the difficulties in translating them into clinical settings, and offers some prospective suggestions for the future on achieving their full therapeutic potential.</abstract><cop>Malaysia</cop><pub>Penerbit Universiti Sains Malaysia</pub><pmid>39416732</pmid><doi>10.21315/mjms2024.31.5.5</doi><tpages>27</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1394-195X
ispartof The Malaysian journal of medical sciences, 2024-10, Vol.31 (5), p.56-82
issn 1394-195X
2180-4303
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_11477465
source DOAJ Directory of Open Access Journals; Bioline International; EZB-FREE-00999 freely available EZB journals; PubMed Central
subjects Review
title Engineered Mesenchymal Stem Cells as Treatment for Cancers: Opportunities, Clinical Applications and Challenges
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T07%3A38%3A40IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Engineered%20Mesenchymal%20Stem%20Cells%20as%20Treatment%20for%20Cancers:%20Opportunities,%20Clinical%20Applications%20and%20Challenges&rft.jtitle=The%20Malaysian%20journal%20of%20medical%20sciences&rft.au=Shamsul%20Kamal,%20Aishah%20Amirah&rft.aucorp=Haematology%20Unit,%20Cancer%20Research%20Centre,%20Institute%20for%20Medical%20Research,%20National%20Institutes%20of%20Health,%20Ministry%20of%20Health%20Malaysia,%20Selangor,%20Malaysia&rft.date=2024-10-01&rft.volume=31&rft.issue=5&rft.spage=56&rft.epage=82&rft.pages=56-82&rft.issn=1394-195X&rft.eissn=2180-4303&rft_id=info:doi/10.21315/mjms2024.31.5.5&rft_dat=%3Cproquest_pubme%3E3117620136%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=3117620136&rft_id=info:pmid/39416732&rfr_iscdi=true