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Osimertinib regressed an EGFR-mutant lung-adenocarcinoma bone-metastasis mouse model and increased long-term survival
Bone is one of the most frequent metastatic sites in non-small cell lung cancer (NSCLC). Osimertinib, with and without bevacizumab (BV), has been investigated on advanced NSCLC patients. However, the efficacy of those drugs on bone metastasis of NSCLC has not been investigated. The human NSCLC cell...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Neoplasia Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7356269/ https://www.ncbi.nlm.nih.gov/pubmed/32659740 http://dx.doi.org/10.1016/j.tranon.2020.100826 |
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author | Higuchi, Takashi Sugisawa, Norihiko Park, Jun Ho Sun, Yu Zhu, Guangwei Yamamoto, Norio Hayashi, Katsuhiro Kimura, Hiroaki Miwa, Shinji Igarashi, Kentaro Bouvet, Michael Singh, Shree Ram Tsuchiya, Hiroyuki Hoffman, Robert M. |
author_facet | Higuchi, Takashi Sugisawa, Norihiko Park, Jun Ho Sun, Yu Zhu, Guangwei Yamamoto, Norio Hayashi, Katsuhiro Kimura, Hiroaki Miwa, Shinji Igarashi, Kentaro Bouvet, Michael Singh, Shree Ram Tsuchiya, Hiroyuki Hoffman, Robert M. |
author_sort | Higuchi, Takashi |
collection | PubMed |
description | Bone is one of the most frequent metastatic sites in non-small cell lung cancer (NSCLC). Osimertinib, with and without bevacizumab (BV), has been investigated on advanced NSCLC patients. However, the efficacy of those drugs on bone metastasis of NSCLC has not been investigated. The human NSCLC cell line H1975, expressing red fluorescent protein (H1975-RFP), was orthotopically injected to the tibia of nude mice. The established mouse models were randomized into four treatment groups of nine mice: Control; BV alone; osimertinib alone; osimertinib and BV combination. The tumors were observed by non-invasive fluorescence imaging. Osimertinib, with or without BV, caused tumor regression, increased mouse survival, and bone remodeling in the bone metastasis models. These results suggest that osimertinib is a promising clinical option for NSCLS patients with bone metastasis. |
format | Online Article Text |
id | pubmed-7356269 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Neoplasia Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-73562692020-07-20 Osimertinib regressed an EGFR-mutant lung-adenocarcinoma bone-metastasis mouse model and increased long-term survival Higuchi, Takashi Sugisawa, Norihiko Park, Jun Ho Sun, Yu Zhu, Guangwei Yamamoto, Norio Hayashi, Katsuhiro Kimura, Hiroaki Miwa, Shinji Igarashi, Kentaro Bouvet, Michael Singh, Shree Ram Tsuchiya, Hiroyuki Hoffman, Robert M. Transl Oncol Original article Bone is one of the most frequent metastatic sites in non-small cell lung cancer (NSCLC). Osimertinib, with and without bevacizumab (BV), has been investigated on advanced NSCLC patients. However, the efficacy of those drugs on bone metastasis of NSCLC has not been investigated. The human NSCLC cell line H1975, expressing red fluorescent protein (H1975-RFP), was orthotopically injected to the tibia of nude mice. The established mouse models were randomized into four treatment groups of nine mice: Control; BV alone; osimertinib alone; osimertinib and BV combination. The tumors were observed by non-invasive fluorescence imaging. Osimertinib, with or without BV, caused tumor regression, increased mouse survival, and bone remodeling in the bone metastasis models. These results suggest that osimertinib is a promising clinical option for NSCLS patients with bone metastasis. Neoplasia Press 2020-07-10 /pmc/articles/PMC7356269/ /pubmed/32659740 http://dx.doi.org/10.1016/j.tranon.2020.100826 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original article Higuchi, Takashi Sugisawa, Norihiko Park, Jun Ho Sun, Yu Zhu, Guangwei Yamamoto, Norio Hayashi, Katsuhiro Kimura, Hiroaki Miwa, Shinji Igarashi, Kentaro Bouvet, Michael Singh, Shree Ram Tsuchiya, Hiroyuki Hoffman, Robert M. Osimertinib regressed an EGFR-mutant lung-adenocarcinoma bone-metastasis mouse model and increased long-term survival |
title | Osimertinib regressed an EGFR-mutant lung-adenocarcinoma bone-metastasis mouse model and increased long-term survival |
title_full | Osimertinib regressed an EGFR-mutant lung-adenocarcinoma bone-metastasis mouse model and increased long-term survival |
title_fullStr | Osimertinib regressed an EGFR-mutant lung-adenocarcinoma bone-metastasis mouse model and increased long-term survival |
title_full_unstemmed | Osimertinib regressed an EGFR-mutant lung-adenocarcinoma bone-metastasis mouse model and increased long-term survival |
title_short | Osimertinib regressed an EGFR-mutant lung-adenocarcinoma bone-metastasis mouse model and increased long-term survival |
title_sort | osimertinib regressed an egfr-mutant lung-adenocarcinoma bone-metastasis mouse model and increased long-term survival |
topic | Original article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7356269/ https://www.ncbi.nlm.nih.gov/pubmed/32659740 http://dx.doi.org/10.1016/j.tranon.2020.100826 |
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