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Pseudotime dynamics of T cells in pancreatic ductal adenocarcinoma inform distinct functional states within the regulatory and cytotoxic T cells
Pancreatic ductal adenocarcinoma (PDAC) is among the deadliest types of cancer and has a 5-year survival of less than 8% owing to its complex biology. As PDAC is refractory to immunotherapy, we need to understand the functional dynamics of T cells in the PDAC microenvironment to develop alternative...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10034436/ https://www.ncbi.nlm.nih.gov/pubmed/36968070 http://dx.doi.org/10.1016/j.isci.2023.106324 |
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author | Jainarayanan, Ashwin Mouroug-Anand, Nithishwer Arbe-Barnes, Edward H. Bush, Adam J. Bashford-Rogers, Rachael Frampton, Adam Heij, Lara Middleton, Mark Dustin, Michael L. Abu-Shah, Enas Sivakumar, Shivan |
author_facet | Jainarayanan, Ashwin Mouroug-Anand, Nithishwer Arbe-Barnes, Edward H. Bush, Adam J. Bashford-Rogers, Rachael Frampton, Adam Heij, Lara Middleton, Mark Dustin, Michael L. Abu-Shah, Enas Sivakumar, Shivan |
author_sort | Jainarayanan, Ashwin |
collection | PubMed |
description | Pancreatic ductal adenocarcinoma (PDAC) is among the deadliest types of cancer and has a 5-year survival of less than 8% owing to its complex biology. As PDAC is refractory to immunotherapy, we need to understand the functional dynamics of T cells in the PDAC microenvironment to develop alternative therapeutic strategies. In this study, we performed RNA velocity-based pseudotime analysis on a scRNA-seq dataset from surgically resected human PDAC specimens to gain insight into temporal gene expression patterns that best characterize the cell fates. The tumor microenvironment was seen to encompass a range of terminal states for the T cell trajectories with suppressive and non-tumor-responsive T cells dominating them. However, the results also reveal the existence of a functional branch of the T cell population that was not transitioning to exhausted and senescent states. These findings reveal various microenvironmental signals driving T cell patterns which can be useful in identifying new therapeutic avenues. |
format | Online Article Text |
id | pubmed-10034436 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-100344362023-03-24 Pseudotime dynamics of T cells in pancreatic ductal adenocarcinoma inform distinct functional states within the regulatory and cytotoxic T cells Jainarayanan, Ashwin Mouroug-Anand, Nithishwer Arbe-Barnes, Edward H. Bush, Adam J. Bashford-Rogers, Rachael Frampton, Adam Heij, Lara Middleton, Mark Dustin, Michael L. Abu-Shah, Enas Sivakumar, Shivan iScience Article Pancreatic ductal adenocarcinoma (PDAC) is among the deadliest types of cancer and has a 5-year survival of less than 8% owing to its complex biology. As PDAC is refractory to immunotherapy, we need to understand the functional dynamics of T cells in the PDAC microenvironment to develop alternative therapeutic strategies. In this study, we performed RNA velocity-based pseudotime analysis on a scRNA-seq dataset from surgically resected human PDAC specimens to gain insight into temporal gene expression patterns that best characterize the cell fates. The tumor microenvironment was seen to encompass a range of terminal states for the T cell trajectories with suppressive and non-tumor-responsive T cells dominating them. However, the results also reveal the existence of a functional branch of the T cell population that was not transitioning to exhausted and senescent states. These findings reveal various microenvironmental signals driving T cell patterns which can be useful in identifying new therapeutic avenues. Elsevier 2023-03-07 /pmc/articles/PMC10034436/ /pubmed/36968070 http://dx.doi.org/10.1016/j.isci.2023.106324 Text en Crown Copyright © 2023. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Jainarayanan, Ashwin Mouroug-Anand, Nithishwer Arbe-Barnes, Edward H. Bush, Adam J. Bashford-Rogers, Rachael Frampton, Adam Heij, Lara Middleton, Mark Dustin, Michael L. Abu-Shah, Enas Sivakumar, Shivan Pseudotime dynamics of T cells in pancreatic ductal adenocarcinoma inform distinct functional states within the regulatory and cytotoxic T cells |
title | Pseudotime dynamics of T cells in pancreatic ductal adenocarcinoma inform distinct functional states within the regulatory and cytotoxic T cells |
title_full | Pseudotime dynamics of T cells in pancreatic ductal adenocarcinoma inform distinct functional states within the regulatory and cytotoxic T cells |
title_fullStr | Pseudotime dynamics of T cells in pancreatic ductal adenocarcinoma inform distinct functional states within the regulatory and cytotoxic T cells |
title_full_unstemmed | Pseudotime dynamics of T cells in pancreatic ductal adenocarcinoma inform distinct functional states within the regulatory and cytotoxic T cells |
title_short | Pseudotime dynamics of T cells in pancreatic ductal adenocarcinoma inform distinct functional states within the regulatory and cytotoxic T cells |
title_sort | pseudotime dynamics of t cells in pancreatic ductal adenocarcinoma inform distinct functional states within the regulatory and cytotoxic t cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10034436/ https://www.ncbi.nlm.nih.gov/pubmed/36968070 http://dx.doi.org/10.1016/j.isci.2023.106324 |
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