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Gastrointestinal cancer stem cells as targets for innovative immunotherapy
The role of cancer stem cells in gastrointestinal cancer-associated death has been widely recognized. Gastrointestinal cancer stem cells (GCSCs) are considered to be responsible for tumor initiation, growth, resistance to cytotoxic therapies, recurrence and metastasis due to their unique properties....
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7167409/ https://www.ncbi.nlm.nih.gov/pubmed/32327907 http://dx.doi.org/10.3748/wjg.v26.i14.1580 |
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author | Chivu-Economescu, Mihaela Necula, Laura G Matei, Lilia Dragu, Denisa Laura Neagu, Ana I Alexiu, Irina Bleotu, Coralia Diaconu, Carmen Cristina |
author_facet | Chivu-Economescu, Mihaela Necula, Laura G Matei, Lilia Dragu, Denisa Laura Neagu, Ana I Alexiu, Irina Bleotu, Coralia Diaconu, Carmen Cristina |
author_sort | Chivu-Economescu, Mihaela |
collection | PubMed |
description | The role of cancer stem cells in gastrointestinal cancer-associated death has been widely recognized. Gastrointestinal cancer stem cells (GCSCs) are considered to be responsible for tumor initiation, growth, resistance to cytotoxic therapies, recurrence and metastasis due to their unique properties. These properties make the current therapeutic trials against GCSCs ineffective. Moreover, recent studies have shown that targeting stem cell surface markers or stemness associated pathways might have an additional off-target effect on the immune system. Recent advances in oncology and precision medicine have opened alternative therapeutic strategies in the form of cancer immunotherapy. This approach differs from classical anti-cancer therapy through its mechanism of action involving the activation and use of a functional immune system against tumor cells, instead of aiming physically destruction of cancer cells through radio- or chemotherapy. New immunological approaches for GCSCs targeting involve the use of different immune cells and various immune mechanisms like targeting specific surface antigens, using innate immune cells like the natural killer and T cells, T-cell chimeric antigen receptor technology, dendritic cell vaccine, or immune checkpoint inhibitors. In this respect, better understandings of immune regulatory mechanisms that govern anti-tumor response bring new hope in obtaining long-term remission for cancer therapy. |
format | Online Article Text |
id | pubmed-7167409 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-71674092020-04-23 Gastrointestinal cancer stem cells as targets for innovative immunotherapy Chivu-Economescu, Mihaela Necula, Laura G Matei, Lilia Dragu, Denisa Laura Neagu, Ana I Alexiu, Irina Bleotu, Coralia Diaconu, Carmen Cristina World J Gastroenterol Review The role of cancer stem cells in gastrointestinal cancer-associated death has been widely recognized. Gastrointestinal cancer stem cells (GCSCs) are considered to be responsible for tumor initiation, growth, resistance to cytotoxic therapies, recurrence and metastasis due to their unique properties. These properties make the current therapeutic trials against GCSCs ineffective. Moreover, recent studies have shown that targeting stem cell surface markers or stemness associated pathways might have an additional off-target effect on the immune system. Recent advances in oncology and precision medicine have opened alternative therapeutic strategies in the form of cancer immunotherapy. This approach differs from classical anti-cancer therapy through its mechanism of action involving the activation and use of a functional immune system against tumor cells, instead of aiming physically destruction of cancer cells through radio- or chemotherapy. New immunological approaches for GCSCs targeting involve the use of different immune cells and various immune mechanisms like targeting specific surface antigens, using innate immune cells like the natural killer and T cells, T-cell chimeric antigen receptor technology, dendritic cell vaccine, or immune checkpoint inhibitors. In this respect, better understandings of immune regulatory mechanisms that govern anti-tumor response bring new hope in obtaining long-term remission for cancer therapy. Baishideng Publishing Group Inc 2020-04-14 2020-04-14 /pmc/articles/PMC7167409/ /pubmed/32327907 http://dx.doi.org/10.3748/wjg.v26.i14.1580 Text en ©The Author(s) 2020. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Review Chivu-Economescu, Mihaela Necula, Laura G Matei, Lilia Dragu, Denisa Laura Neagu, Ana I Alexiu, Irina Bleotu, Coralia Diaconu, Carmen Cristina Gastrointestinal cancer stem cells as targets for innovative immunotherapy |
title | Gastrointestinal cancer stem cells as targets for innovative immunotherapy |
title_full | Gastrointestinal cancer stem cells as targets for innovative immunotherapy |
title_fullStr | Gastrointestinal cancer stem cells as targets for innovative immunotherapy |
title_full_unstemmed | Gastrointestinal cancer stem cells as targets for innovative immunotherapy |
title_short | Gastrointestinal cancer stem cells as targets for innovative immunotherapy |
title_sort | gastrointestinal cancer stem cells as targets for innovative immunotherapy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7167409/ https://www.ncbi.nlm.nih.gov/pubmed/32327907 http://dx.doi.org/10.3748/wjg.v26.i14.1580 |
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