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Lenvatinib Promotes the Antitumor Effect of Doxorubicin in Anaplastic Thyroid Cancer
PURPOSE: Anaplastic thyroid cancer (ATC) is a kind of rare thyroid cancer with very poor prognosis. Doxorubicin has been approved in ATC treatment as a single agent, but monotherapy still shows no improvement of the total survival in advanced ATC. Lenvatinib was investigated with encouraging results...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7646435/ https://www.ncbi.nlm.nih.gov/pubmed/33173310 http://dx.doi.org/10.2147/OTT.S278349 |
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author | Su, Xi Liu, Jiaxin Zhang, Haihong Gu, Qingqing Zhou, Xinrui Ji, Meiju Yao, Demao |
author_facet | Su, Xi Liu, Jiaxin Zhang, Haihong Gu, Qingqing Zhou, Xinrui Ji, Meiju Yao, Demao |
author_sort | Su, Xi |
collection | PubMed |
description | PURPOSE: Anaplastic thyroid cancer (ATC) is a kind of rare thyroid cancer with very poor prognosis. Doxorubicin has been approved in ATC treatment as a single agent, but monotherapy still shows no improvement of the total survival in advanced ATC. Lenvatinib was investigated with encouraging results in treating patients with radioiodine-refractory differentiated thyroid cancer (DTC). However, antitumor efficacy of combination therapy with lenvatinib and doxorubicin remains largely unclear. MATERIALS AND METHODS: The antitumor efficacy of combination therapy with lenvatinib and doxorubicin on ATC cell proliferation was assessed by the MTT assay and colony formation. Flow cytometry was employed to assess ATC cells’ apoptosis and cell cycle arrest in response to combination therapy. Transwell assay was used to test the migration and invasion in response to combination therapy. Xenograft models were used to test its in vivo antitumor activity. RESULTS: Lenvatinib monotherapy was less effective than doxorubicin in treating ATC cell lines and xenograft model. The combination therapy of lenvatinib and doxorubicin significantly inhibited ATC cell proliferation and tumor growth in nude mice, and induced cell apoptosis and cell cycle arrest as compared to lenvatinib or doxorubicin monotherapy. CONCLUSION: Lenvatinib promotes the antitumor effect of doxorubicin in ATC cell and xenograft model. The lenvatinib/doxorubicin combination may be a potential candidate therapeutic approach for anaplastic thyroid cancer. |
format | Online Article Text |
id | pubmed-7646435 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-76464352020-11-09 Lenvatinib Promotes the Antitumor Effect of Doxorubicin in Anaplastic Thyroid Cancer Su, Xi Liu, Jiaxin Zhang, Haihong Gu, Qingqing Zhou, Xinrui Ji, Meiju Yao, Demao Onco Targets Ther Original Research PURPOSE: Anaplastic thyroid cancer (ATC) is a kind of rare thyroid cancer with very poor prognosis. Doxorubicin has been approved in ATC treatment as a single agent, but monotherapy still shows no improvement of the total survival in advanced ATC. Lenvatinib was investigated with encouraging results in treating patients with radioiodine-refractory differentiated thyroid cancer (DTC). However, antitumor efficacy of combination therapy with lenvatinib and doxorubicin remains largely unclear. MATERIALS AND METHODS: The antitumor efficacy of combination therapy with lenvatinib and doxorubicin on ATC cell proliferation was assessed by the MTT assay and colony formation. Flow cytometry was employed to assess ATC cells’ apoptosis and cell cycle arrest in response to combination therapy. Transwell assay was used to test the migration and invasion in response to combination therapy. Xenograft models were used to test its in vivo antitumor activity. RESULTS: Lenvatinib monotherapy was less effective than doxorubicin in treating ATC cell lines and xenograft model. The combination therapy of lenvatinib and doxorubicin significantly inhibited ATC cell proliferation and tumor growth in nude mice, and induced cell apoptosis and cell cycle arrest as compared to lenvatinib or doxorubicin monotherapy. CONCLUSION: Lenvatinib promotes the antitumor effect of doxorubicin in ATC cell and xenograft model. The lenvatinib/doxorubicin combination may be a potential candidate therapeutic approach for anaplastic thyroid cancer. Dove 2020-11-02 /pmc/articles/PMC7646435/ /pubmed/33173310 http://dx.doi.org/10.2147/OTT.S278349 Text en © 2020 Su et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Su, Xi Liu, Jiaxin Zhang, Haihong Gu, Qingqing Zhou, Xinrui Ji, Meiju Yao, Demao Lenvatinib Promotes the Antitumor Effect of Doxorubicin in Anaplastic Thyroid Cancer |
title | Lenvatinib Promotes the Antitumor Effect of Doxorubicin in Anaplastic Thyroid Cancer |
title_full | Lenvatinib Promotes the Antitumor Effect of Doxorubicin in Anaplastic Thyroid Cancer |
title_fullStr | Lenvatinib Promotes the Antitumor Effect of Doxorubicin in Anaplastic Thyroid Cancer |
title_full_unstemmed | Lenvatinib Promotes the Antitumor Effect of Doxorubicin in Anaplastic Thyroid Cancer |
title_short | Lenvatinib Promotes the Antitumor Effect of Doxorubicin in Anaplastic Thyroid Cancer |
title_sort | lenvatinib promotes the antitumor effect of doxorubicin in anaplastic thyroid cancer |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7646435/ https://www.ncbi.nlm.nih.gov/pubmed/33173310 http://dx.doi.org/10.2147/OTT.S278349 |
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