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RanBP1: A Potential Therapeutic Target for Cancer Stem Cells in Lung Cancer and Glioma
Cancer stem cells (CSCs) are known to be one of the factors that make cancer treatment difficult. Many researchers are thus conducting research to efficiently destroy CSCs. Therefore, we sought to suggest a new target that can efficiently suppress CSCs. In this study, we observed a high expression o...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10095367/ https://www.ncbi.nlm.nih.gov/pubmed/37047826 http://dx.doi.org/10.3390/ijms24076855 |
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author | Kahm, Yeon-Jee Kim, In-Gyu Kim, Rae-Kwon |
author_facet | Kahm, Yeon-Jee Kim, In-Gyu Kim, Rae-Kwon |
author_sort | Kahm, Yeon-Jee |
collection | PubMed |
description | Cancer stem cells (CSCs) are known to be one of the factors that make cancer treatment difficult. Many researchers are thus conducting research to efficiently destroy CSCs. Therefore, we sought to suggest a new target that can efficiently suppress CSCs. In this study, we observed a high expression of Ran-binding protein 1 (RanBP1) in lung cancer stem cells (LCSCs) and glioma stem cells (GSCs). Upregulated RanBP1 expression is strongly associated with the expression of CSC marker proteins and CSC regulators. In addition, an elevated RanBP1 expression is strongly associated with a poor patient prognosis. CSCs have the ability to resist radiation, and RanBP1 regulates this ability. RanBP1 also affects the metastasis-associated epithelial–mesenchymal transition (EMT) phenomenon. EMT marker proteins and regulatory proteins are affected by RanBP1 expression, and cell motility was regulated according to RanBP1 expression. The cancer microenvironment influences cancer growth, metastasis, and cancer treatment. RanBP1 can modulate the cancer microenvironment by regulating the cytokine IL-18. Secreted IL-18 acts on cancer cells and promotes cancer malignancy. Our results reveal, for the first time, that RanBP1 is an important regulator in LCSCs and GSCs, suggesting that it holds potential for use as a potential therapeutic target. |
format | Online Article Text |
id | pubmed-10095367 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-100953672023-04-13 RanBP1: A Potential Therapeutic Target for Cancer Stem Cells in Lung Cancer and Glioma Kahm, Yeon-Jee Kim, In-Gyu Kim, Rae-Kwon Int J Mol Sci Article Cancer stem cells (CSCs) are known to be one of the factors that make cancer treatment difficult. Many researchers are thus conducting research to efficiently destroy CSCs. Therefore, we sought to suggest a new target that can efficiently suppress CSCs. In this study, we observed a high expression of Ran-binding protein 1 (RanBP1) in lung cancer stem cells (LCSCs) and glioma stem cells (GSCs). Upregulated RanBP1 expression is strongly associated with the expression of CSC marker proteins and CSC regulators. In addition, an elevated RanBP1 expression is strongly associated with a poor patient prognosis. CSCs have the ability to resist radiation, and RanBP1 regulates this ability. RanBP1 also affects the metastasis-associated epithelial–mesenchymal transition (EMT) phenomenon. EMT marker proteins and regulatory proteins are affected by RanBP1 expression, and cell motility was regulated according to RanBP1 expression. The cancer microenvironment influences cancer growth, metastasis, and cancer treatment. RanBP1 can modulate the cancer microenvironment by regulating the cytokine IL-18. Secreted IL-18 acts on cancer cells and promotes cancer malignancy. Our results reveal, for the first time, that RanBP1 is an important regulator in LCSCs and GSCs, suggesting that it holds potential for use as a potential therapeutic target. MDPI 2023-04-06 /pmc/articles/PMC10095367/ /pubmed/37047826 http://dx.doi.org/10.3390/ijms24076855 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kahm, Yeon-Jee Kim, In-Gyu Kim, Rae-Kwon RanBP1: A Potential Therapeutic Target for Cancer Stem Cells in Lung Cancer and Glioma |
title | RanBP1: A Potential Therapeutic Target for Cancer Stem Cells in Lung Cancer and Glioma |
title_full | RanBP1: A Potential Therapeutic Target for Cancer Stem Cells in Lung Cancer and Glioma |
title_fullStr | RanBP1: A Potential Therapeutic Target for Cancer Stem Cells in Lung Cancer and Glioma |
title_full_unstemmed | RanBP1: A Potential Therapeutic Target for Cancer Stem Cells in Lung Cancer and Glioma |
title_short | RanBP1: A Potential Therapeutic Target for Cancer Stem Cells in Lung Cancer and Glioma |
title_sort | ranbp1: a potential therapeutic target for cancer stem cells in lung cancer and glioma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10095367/ https://www.ncbi.nlm.nih.gov/pubmed/37047826 http://dx.doi.org/10.3390/ijms24076855 |
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