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Are ovarian cancer stem cells the target for innovative immunotherapy?
Cancer stem cells (CSCs), a subpopulation of cancer cells with the ability of self-renewal and differentiation, are believed to be responsible for tumor generation, progression, metastasis, and relapse. Ovarian cancer, the most malignant gynecological cancer, has consistent pathology behavior with C...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5951213/ https://www.ncbi.nlm.nih.gov/pubmed/29780254 http://dx.doi.org/10.2147/OTT.S155458 |
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author | Wang, Liang Xu, Tianmin Cui, Manhua |
author_facet | Wang, Liang Xu, Tianmin Cui, Manhua |
author_sort | Wang, Liang |
collection | PubMed |
description | Cancer stem cells (CSCs), a subpopulation of cancer cells with the ability of self-renewal and differentiation, are believed to be responsible for tumor generation, progression, metastasis, and relapse. Ovarian cancer, the most malignant gynecological cancer, has consistent pathology behavior with CSC model, which suggests that therapies based on ovarian cancer stem cells (OCSCs) can gain a more successful prognosis. Much evidence has proved that epigenetic mechanism played an important role in tumor formation and sustainment. Since CSCs are generally resistant to conventional therapies (chemotherapy and radiotherapy), immunotherapy is a more effective method that has been implemented in the clinic. Chimeric antigen receptor (CAR)-T cell, an adoptive cellular immunotherapy, which results in apparent elimination of tumor in both hematologic and solid cancers, could be used for ovarian cancer. This review covers the basic conception of CSCs and OCSCs, the implication of epigenetic mechanism underlying cancer evolution considering CSC model, the immunotherapies reported for ovarian cancer targeting OCSCs currently, and the relationship between immune system and hierarchy cancer organized by CSCs. Particularly, the promising prospects and potential pitfalls of targeting OCSC surface markers to design CAR-T cellular immunotherapy are discussed here. |
format | Online Article Text |
id | pubmed-5951213 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-59512132018-05-18 Are ovarian cancer stem cells the target for innovative immunotherapy? Wang, Liang Xu, Tianmin Cui, Manhua Onco Targets Ther Review Cancer stem cells (CSCs), a subpopulation of cancer cells with the ability of self-renewal and differentiation, are believed to be responsible for tumor generation, progression, metastasis, and relapse. Ovarian cancer, the most malignant gynecological cancer, has consistent pathology behavior with CSC model, which suggests that therapies based on ovarian cancer stem cells (OCSCs) can gain a more successful prognosis. Much evidence has proved that epigenetic mechanism played an important role in tumor formation and sustainment. Since CSCs are generally resistant to conventional therapies (chemotherapy and radiotherapy), immunotherapy is a more effective method that has been implemented in the clinic. Chimeric antigen receptor (CAR)-T cell, an adoptive cellular immunotherapy, which results in apparent elimination of tumor in both hematologic and solid cancers, could be used for ovarian cancer. This review covers the basic conception of CSCs and OCSCs, the implication of epigenetic mechanism underlying cancer evolution considering CSC model, the immunotherapies reported for ovarian cancer targeting OCSCs currently, and the relationship between immune system and hierarchy cancer organized by CSCs. Particularly, the promising prospects and potential pitfalls of targeting OCSC surface markers to design CAR-T cellular immunotherapy are discussed here. Dove Medical Press 2018-05-08 /pmc/articles/PMC5951213/ /pubmed/29780254 http://dx.doi.org/10.2147/OTT.S155458 Text en © 2018 Wang et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Review Wang, Liang Xu, Tianmin Cui, Manhua Are ovarian cancer stem cells the target for innovative immunotherapy? |
title | Are ovarian cancer stem cells the target for innovative immunotherapy? |
title_full | Are ovarian cancer stem cells the target for innovative immunotherapy? |
title_fullStr | Are ovarian cancer stem cells the target for innovative immunotherapy? |
title_full_unstemmed | Are ovarian cancer stem cells the target for innovative immunotherapy? |
title_short | Are ovarian cancer stem cells the target for innovative immunotherapy? |
title_sort | are ovarian cancer stem cells the target for innovative immunotherapy? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5951213/ https://www.ncbi.nlm.nih.gov/pubmed/29780254 http://dx.doi.org/10.2147/OTT.S155458 |
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