The Potential of Induced Pluripotent Stem Cells to Advance the Treatment of Pancreatic Ductal Adenocarcinoma
Advances in the treatment of pancreatic ductal adenocarcinoma (PDAC) using neoadjuvant chemoradiotherapy, chemotherapy, and immunotherapy have had minimal impact on the overall survival of patients. A general lack of immunogenic features and a complex tumor microenvironment (TME) are likely culprits...
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MDPI AG
2021
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oai:doaj.org-article:c4d760c6828849d491c2f1224e656a402021-11-25T17:04:01ZThe Potential of Induced Pluripotent Stem Cells to Advance the Treatment of Pancreatic Ductal Adenocarcinoma10.3390/cancers132257892072-6694https://doaj.org/article/c4d760c6828849d491c2f1224e656a402021-11-01T00:00:00Zhttps://www.mdpi.com/2072-6694/13/22/5789https://doaj.org/toc/2072-6694Advances in the treatment of pancreatic ductal adenocarcinoma (PDAC) using neoadjuvant chemoradiotherapy, chemotherapy, and immunotherapy have had minimal impact on the overall survival of patients. A general lack of immunogenic features and a complex tumor microenvironment (TME) are likely culprits for therapy refractoriness in PDAC. Induced pluripotent stem cells (iPSCs) should be explored as a means to advance the treatment options for PDAC, by providing representative in vitro models of pancreatic cancer development. In addition, iPSCs could be used for tailor-made cellular immunotherapies or as a source of tumor-associated antigens in the context of vaccination.Ricki T. KrogNoel F. C. C. de MirandaAlexander L. VahrmeijerNigel G. KooremanMDPI AGarticlepancreatic ductal adenocarcinomaPDACinduced pluripotent stem cellsiPSCscancer modelscancer vaccineNeoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENCancers, Vol 13, Iss 5789, p 5789 (2021) |
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DOAJ |
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pancreatic ductal adenocarcinoma PDAC induced pluripotent stem cells iPSCs cancer models cancer vaccine Neoplasms. Tumors. Oncology. Including cancer and carcinogens RC254-282 |
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pancreatic ductal adenocarcinoma PDAC induced pluripotent stem cells iPSCs cancer models cancer vaccine Neoplasms. Tumors. Oncology. Including cancer and carcinogens RC254-282 Ricki T. Krog Noel F. C. C. de Miranda Alexander L. Vahrmeijer Nigel G. Kooreman The Potential of Induced Pluripotent Stem Cells to Advance the Treatment of Pancreatic Ductal Adenocarcinoma |
description |
Advances in the treatment of pancreatic ductal adenocarcinoma (PDAC) using neoadjuvant chemoradiotherapy, chemotherapy, and immunotherapy have had minimal impact on the overall survival of patients. A general lack of immunogenic features and a complex tumor microenvironment (TME) are likely culprits for therapy refractoriness in PDAC. Induced pluripotent stem cells (iPSCs) should be explored as a means to advance the treatment options for PDAC, by providing representative in vitro models of pancreatic cancer development. In addition, iPSCs could be used for tailor-made cellular immunotherapies or as a source of tumor-associated antigens in the context of vaccination. |
format |
article |
author |
Ricki T. Krog Noel F. C. C. de Miranda Alexander L. Vahrmeijer Nigel G. Kooreman |
author_facet |
Ricki T. Krog Noel F. C. C. de Miranda Alexander L. Vahrmeijer Nigel G. Kooreman |
author_sort |
Ricki T. Krog |
title |
The Potential of Induced Pluripotent Stem Cells to Advance the Treatment of Pancreatic Ductal Adenocarcinoma |
title_short |
The Potential of Induced Pluripotent Stem Cells to Advance the Treatment of Pancreatic Ductal Adenocarcinoma |
title_full |
The Potential of Induced Pluripotent Stem Cells to Advance the Treatment of Pancreatic Ductal Adenocarcinoma |
title_fullStr |
The Potential of Induced Pluripotent Stem Cells to Advance the Treatment of Pancreatic Ductal Adenocarcinoma |
title_full_unstemmed |
The Potential of Induced Pluripotent Stem Cells to Advance the Treatment of Pancreatic Ductal Adenocarcinoma |
title_sort |
potential of induced pluripotent stem cells to advance the treatment of pancreatic ductal adenocarcinoma |
publisher |
MDPI AG |
publishDate |
2021 |
url |
https://doaj.org/article/c4d760c6828849d491c2f1224e656a40 |
work_keys_str_mv |
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