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α-Catulin promotes cancer stemness by antagonizing WWP1-mediated KLF5 degradation in lung cancer
Background: The cytoskeletal linker protein α-Catulin has been shown to be important for tumor progression in various cancers. However, its role in the regulation of cancer stemness remains unclear. Methods: Phenotypic effects of α-Catulin on the cancer stem cell (CSC)-like properties and metastasis...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8771551/ https://www.ncbi.nlm.nih.gov/pubmed/35154481 http://dx.doi.org/10.7150/thno.63627 |
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author | Tung, Chia-Hao Huang, Meng-Fan Liang, Chen-Hsien Wu, Yi-Ying Wu, Jia-En Hsu, Cheng-Lung Chen, Yuh-Ling Hong, Tse-Ming |
author_facet | Tung, Chia-Hao Huang, Meng-Fan Liang, Chen-Hsien Wu, Yi-Ying Wu, Jia-En Hsu, Cheng-Lung Chen, Yuh-Ling Hong, Tse-Ming |
author_sort | Tung, Chia-Hao |
collection | PubMed |
description | Background: The cytoskeletal linker protein α-Catulin has been shown to be important for tumor progression in various cancers. However, its role in the regulation of cancer stemness remains unclear. Methods: Phenotypic effects of α-Catulin on the cancer stem cell (CSC)-like properties and metastasis were examined by in vitro sphere formation assay, migration assay, invasion assay, and in vivo xenografted animal models. Yeast two-hybrid assay, co-immunoprecipitation assay, and cycloheximide chase assay were performed to confirm the effect of α-Catulin on the WWP1-mediated degradation of KLF5. CPTAC and TCGA database were analyzed to determine the clinical association of α-Catulin, KLF5, and stemness-associated signatures in lung adenocarcinoma. Results: We report that α-Catulin increases cancer stem-like properties in non-small cell lung cancer (NSCLC). The expression of α-Catulin is elevated in tumor spheres compared to sphere-derived adherent cells and promotes the acquisition of cancer stemness characteristics in vitro and in vivo. Mechanistically, the interaction of α-Catulin and the C-terminal region of Kruppel-like transcription factor KLF5 results in the inhibition of WWP1-mediated degradation of KLF5. Accordingly, increased protein expression of KLF5 is observed in clinical specimens of lung adenocarcinoma with high expression of α-Catulin compared to specimens with low α-Catulin-expression. Knockdown of KLF5 abrogates α-Catulin-driven cancer stemness. α-Catulin is known to interact with integrin-linked kinase (ILK). Notably, an ILK inhibitor disrupts the α-Catulin-KLF5 interaction, promotes the degradation of KLF5, and decreases α-Catulin-driven cancer stemness. Importantly, we identify a CTNNAL1/ILK/KLF5 three-gene signature for predicting poor overall survival in patients with lung adenocarcinoma. Conclusions: These findings reveal a molecular basis of α-Catulin-enhanced KLF5 signaling and highlight a role for α-Catulin in promoting cancer stemness. |
format | Online Article Text |
id | pubmed-8771551 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-87715512022-02-10 α-Catulin promotes cancer stemness by antagonizing WWP1-mediated KLF5 degradation in lung cancer Tung, Chia-Hao Huang, Meng-Fan Liang, Chen-Hsien Wu, Yi-Ying Wu, Jia-En Hsu, Cheng-Lung Chen, Yuh-Ling Hong, Tse-Ming Theranostics Research Paper Background: The cytoskeletal linker protein α-Catulin has been shown to be important for tumor progression in various cancers. However, its role in the regulation of cancer stemness remains unclear. Methods: Phenotypic effects of α-Catulin on the cancer stem cell (CSC)-like properties and metastasis were examined by in vitro sphere formation assay, migration assay, invasion assay, and in vivo xenografted animal models. Yeast two-hybrid assay, co-immunoprecipitation assay, and cycloheximide chase assay were performed to confirm the effect of α-Catulin on the WWP1-mediated degradation of KLF5. CPTAC and TCGA database were analyzed to determine the clinical association of α-Catulin, KLF5, and stemness-associated signatures in lung adenocarcinoma. Results: We report that α-Catulin increases cancer stem-like properties in non-small cell lung cancer (NSCLC). The expression of α-Catulin is elevated in tumor spheres compared to sphere-derived adherent cells and promotes the acquisition of cancer stemness characteristics in vitro and in vivo. Mechanistically, the interaction of α-Catulin and the C-terminal region of Kruppel-like transcription factor KLF5 results in the inhibition of WWP1-mediated degradation of KLF5. Accordingly, increased protein expression of KLF5 is observed in clinical specimens of lung adenocarcinoma with high expression of α-Catulin compared to specimens with low α-Catulin-expression. Knockdown of KLF5 abrogates α-Catulin-driven cancer stemness. α-Catulin is known to interact with integrin-linked kinase (ILK). Notably, an ILK inhibitor disrupts the α-Catulin-KLF5 interaction, promotes the degradation of KLF5, and decreases α-Catulin-driven cancer stemness. Importantly, we identify a CTNNAL1/ILK/KLF5 three-gene signature for predicting poor overall survival in patients with lung adenocarcinoma. Conclusions: These findings reveal a molecular basis of α-Catulin-enhanced KLF5 signaling and highlight a role for α-Catulin in promoting cancer stemness. Ivyspring International Publisher 2022-01-01 /pmc/articles/PMC8771551/ /pubmed/35154481 http://dx.doi.org/10.7150/thno.63627 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Tung, Chia-Hao Huang, Meng-Fan Liang, Chen-Hsien Wu, Yi-Ying Wu, Jia-En Hsu, Cheng-Lung Chen, Yuh-Ling Hong, Tse-Ming α-Catulin promotes cancer stemness by antagonizing WWP1-mediated KLF5 degradation in lung cancer |
title | α-Catulin promotes cancer stemness by antagonizing WWP1-mediated KLF5 degradation in lung cancer |
title_full | α-Catulin promotes cancer stemness by antagonizing WWP1-mediated KLF5 degradation in lung cancer |
title_fullStr | α-Catulin promotes cancer stemness by antagonizing WWP1-mediated KLF5 degradation in lung cancer |
title_full_unstemmed | α-Catulin promotes cancer stemness by antagonizing WWP1-mediated KLF5 degradation in lung cancer |
title_short | α-Catulin promotes cancer stemness by antagonizing WWP1-mediated KLF5 degradation in lung cancer |
title_sort | α-catulin promotes cancer stemness by antagonizing wwp1-mediated klf5 degradation in lung cancer |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8771551/ https://www.ncbi.nlm.nih.gov/pubmed/35154481 http://dx.doi.org/10.7150/thno.63627 |
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