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Tocilizumab (monoclonal anti-IL-6R antibody) reverses anlotinib resistance in osteosarcoma
PURPOSE: Anlotinib, a tyrosine kinase inhibitor (TKI) has been in clinical application to inhibit malignant cell growth and lung metastasis in osteosarcoma (OS). However, a variety of drug resistance phenomena have been observed in the treatment. We aim to explore the new target to reverse anlotinib...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10315670/ https://www.ncbi.nlm.nih.gov/pubmed/37404767 http://dx.doi.org/10.3389/fonc.2023.1192472 |
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author | Xu, Jiuhui Chen, Chenglong Sun, Kunkun Shi, Qianyu Wang, Boyang Huang, Yi Ren, Tingting Tang, Xiaodong |
author_facet | Xu, Jiuhui Chen, Chenglong Sun, Kunkun Shi, Qianyu Wang, Boyang Huang, Yi Ren, Tingting Tang, Xiaodong |
author_sort | Xu, Jiuhui |
collection | PubMed |
description | PURPOSE: Anlotinib, a tyrosine kinase inhibitor (TKI) has been in clinical application to inhibit malignant cell growth and lung metastasis in osteosarcoma (OS). However, a variety of drug resistance phenomena have been observed in the treatment. We aim to explore the new target to reverse anlotinib resistance in OS. MATERIALS AND METHODS: In this study, we established four OS anlotinib-resistant cell lines, and RNA-sequence was performed to evaluate differentially expressed genes. We verified the results of RNA-sequence by PCR, western blot and ELISA assay. We further explored the effects of tocilizumab (anti- IL-6 receptor), either alone or in combined with anlotinib, on the inhibition of anlotinib-resistant OS cells malignant viability by CCK8, EDU, colony formation, apoptosis, transwell, wound healing, Cytoskeletal stain assays, and xenograft nude mouse model. The expression of IL-6 in 104 osteosarcoma samples was tested by IHC. RESULTS: We found IL-6 and its downstream pathway STAT3 were activated in anlotinib-resistant osteosarcoma. Tocilizumab impaired the tumor progression of anlotinib-resistant OS cells, and combined treatment with anlotinib augmented these effects by inhibiting STAT3 expressions. IL-6 was highly expressed in patients with OS and correlated with poor prognosis. CONCLUSION: Tocilizumab could reverse anlotinib resistance in OS by IL-6/STAT3 pathway and the combination treatment with anlotinib rationalized further studies and clinical treatment of OS. |
format | Online Article Text |
id | pubmed-10315670 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-103156702023-07-04 Tocilizumab (monoclonal anti-IL-6R antibody) reverses anlotinib resistance in osteosarcoma Xu, Jiuhui Chen, Chenglong Sun, Kunkun Shi, Qianyu Wang, Boyang Huang, Yi Ren, Tingting Tang, Xiaodong Front Oncol Oncology PURPOSE: Anlotinib, a tyrosine kinase inhibitor (TKI) has been in clinical application to inhibit malignant cell growth and lung metastasis in osteosarcoma (OS). However, a variety of drug resistance phenomena have been observed in the treatment. We aim to explore the new target to reverse anlotinib resistance in OS. MATERIALS AND METHODS: In this study, we established four OS anlotinib-resistant cell lines, and RNA-sequence was performed to evaluate differentially expressed genes. We verified the results of RNA-sequence by PCR, western blot and ELISA assay. We further explored the effects of tocilizumab (anti- IL-6 receptor), either alone or in combined with anlotinib, on the inhibition of anlotinib-resistant OS cells malignant viability by CCK8, EDU, colony formation, apoptosis, transwell, wound healing, Cytoskeletal stain assays, and xenograft nude mouse model. The expression of IL-6 in 104 osteosarcoma samples was tested by IHC. RESULTS: We found IL-6 and its downstream pathway STAT3 were activated in anlotinib-resistant osteosarcoma. Tocilizumab impaired the tumor progression of anlotinib-resistant OS cells, and combined treatment with anlotinib augmented these effects by inhibiting STAT3 expressions. IL-6 was highly expressed in patients with OS and correlated with poor prognosis. CONCLUSION: Tocilizumab could reverse anlotinib resistance in OS by IL-6/STAT3 pathway and the combination treatment with anlotinib rationalized further studies and clinical treatment of OS. Frontiers Media S.A. 2023-06-19 /pmc/articles/PMC10315670/ /pubmed/37404767 http://dx.doi.org/10.3389/fonc.2023.1192472 Text en Copyright © 2023 Xu, Chen, Sun, Shi, Wang, Huang, Ren and Tang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Xu, Jiuhui Chen, Chenglong Sun, Kunkun Shi, Qianyu Wang, Boyang Huang, Yi Ren, Tingting Tang, Xiaodong Tocilizumab (monoclonal anti-IL-6R antibody) reverses anlotinib resistance in osteosarcoma |
title | Tocilizumab (monoclonal anti-IL-6R antibody) reverses anlotinib resistance in osteosarcoma |
title_full | Tocilizumab (monoclonal anti-IL-6R antibody) reverses anlotinib resistance in osteosarcoma |
title_fullStr | Tocilizumab (monoclonal anti-IL-6R antibody) reverses anlotinib resistance in osteosarcoma |
title_full_unstemmed | Tocilizumab (monoclonal anti-IL-6R antibody) reverses anlotinib resistance in osteosarcoma |
title_short | Tocilizumab (monoclonal anti-IL-6R antibody) reverses anlotinib resistance in osteosarcoma |
title_sort | tocilizumab (monoclonal anti-il-6r antibody) reverses anlotinib resistance in osteosarcoma |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10315670/ https://www.ncbi.nlm.nih.gov/pubmed/37404767 http://dx.doi.org/10.3389/fonc.2023.1192472 |
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