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Leukemia Inhibitory Factor: A Potential Biomarker and Therapeutic Target in Pancreatic Cancer
Pancreatic ductal adenocarcinoma (PDAC) is a highly aggressive, treatment-resistant cancer. Five-year survival rate is about 9%, one of the lowest among all solid tumors. Such a poor outcome is partly due to the limited knowledge of tumor biology, and the resulting lack of effective treatment option...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7907038/ https://www.ncbi.nlm.nih.gov/pubmed/33630157 http://dx.doi.org/10.1007/s00005-021-00605-w |
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author | Wrona, Ewa Potemski, Piotr Sclafani, Francesco Borowiec, Maciej |
author_facet | Wrona, Ewa Potemski, Piotr Sclafani, Francesco Borowiec, Maciej |
author_sort | Wrona, Ewa |
collection | PubMed |
description | Pancreatic ductal adenocarcinoma (PDAC) is a highly aggressive, treatment-resistant cancer. Five-year survival rate is about 9%, one of the lowest among all solid tumors. Such a poor outcome is partly due to the limited knowledge of tumor biology, and the resulting lack of effective treatment options and robust predictive biomarkers. The leukemia inhibitory factor (LIF) has recently emerged as a potential biomarker and therapeutic target for PDAC. Accumulating evidence has suggested that LIF plays a role in supporting cancer evolution as a regulator of cell differentiation, renewal and survival. Interestingly, it can be detected in the serum of PDAC patients at higher concentrations than healthy individuals, this supporting its potential value as diagnostic biomarker. Furthermore, preliminary data indicate that testing for LIF serum concentration or tissue expression may help with treatment response monitoring and prognostication. Finally, studies in PDAC mouse models have also shown that LIF may be a valuable therapeutic target, and first-in-human clinical trial is currently ongoing. This article aims to review the available data on the role of LIF in PDAC promotion, and to discuss the evidence supporting its potential role as a biomarker and target of effective anti-cancer therapy in this setting. |
format | Online Article Text |
id | pubmed-7907038 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-79070382021-03-09 Leukemia Inhibitory Factor: A Potential Biomarker and Therapeutic Target in Pancreatic Cancer Wrona, Ewa Potemski, Piotr Sclafani, Francesco Borowiec, Maciej Arch Immunol Ther Exp (Warsz) Review Pancreatic ductal adenocarcinoma (PDAC) is a highly aggressive, treatment-resistant cancer. Five-year survival rate is about 9%, one of the lowest among all solid tumors. Such a poor outcome is partly due to the limited knowledge of tumor biology, and the resulting lack of effective treatment options and robust predictive biomarkers. The leukemia inhibitory factor (LIF) has recently emerged as a potential biomarker and therapeutic target for PDAC. Accumulating evidence has suggested that LIF plays a role in supporting cancer evolution as a regulator of cell differentiation, renewal and survival. Interestingly, it can be detected in the serum of PDAC patients at higher concentrations than healthy individuals, this supporting its potential value as diagnostic biomarker. Furthermore, preliminary data indicate that testing for LIF serum concentration or tissue expression may help with treatment response monitoring and prognostication. Finally, studies in PDAC mouse models have also shown that LIF may be a valuable therapeutic target, and first-in-human clinical trial is currently ongoing. This article aims to review the available data on the role of LIF in PDAC promotion, and to discuss the evidence supporting its potential role as a biomarker and target of effective anti-cancer therapy in this setting. Springer International Publishing 2021-02-25 2021 /pmc/articles/PMC7907038/ /pubmed/33630157 http://dx.doi.org/10.1007/s00005-021-00605-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Wrona, Ewa Potemski, Piotr Sclafani, Francesco Borowiec, Maciej Leukemia Inhibitory Factor: A Potential Biomarker and Therapeutic Target in Pancreatic Cancer |
title | Leukemia Inhibitory Factor: A Potential Biomarker and Therapeutic Target in Pancreatic Cancer |
title_full | Leukemia Inhibitory Factor: A Potential Biomarker and Therapeutic Target in Pancreatic Cancer |
title_fullStr | Leukemia Inhibitory Factor: A Potential Biomarker and Therapeutic Target in Pancreatic Cancer |
title_full_unstemmed | Leukemia Inhibitory Factor: A Potential Biomarker and Therapeutic Target in Pancreatic Cancer |
title_short | Leukemia Inhibitory Factor: A Potential Biomarker and Therapeutic Target in Pancreatic Cancer |
title_sort | leukemia inhibitory factor: a potential biomarker and therapeutic target in pancreatic cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7907038/ https://www.ncbi.nlm.nih.gov/pubmed/33630157 http://dx.doi.org/10.1007/s00005-021-00605-w |
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