Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Neoplasia Press 2020
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
_version_ 1783558461616816128
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
work_keys_str_mv AT higuchitakashi osimertinibregressedanegfrmutantlungadenocarcinomabonemetastasismousemodelandincreasedlongtermsurvival
AT sugisawanorihiko osimertinibregressedanegfrmutantlungadenocarcinomabonemetastasismousemodelandincreasedlongtermsurvival
AT parkjunho osimertinibregressedanegfrmutantlungadenocarcinomabonemetastasismousemodelandincreasedlongtermsurvival
AT sunyu osimertinibregressedanegfrmutantlungadenocarcinomabonemetastasismousemodelandincreasedlongtermsurvival
AT zhuguangwei osimertinibregressedanegfrmutantlungadenocarcinomabonemetastasismousemodelandincreasedlongtermsurvival
AT yamamotonorio osimertinibregressedanegfrmutantlungadenocarcinomabonemetastasismousemodelandincreasedlongtermsurvival
AT hayashikatsuhiro osimertinibregressedanegfrmutantlungadenocarcinomabonemetastasismousemodelandincreasedlongtermsurvival
AT kimurahiroaki osimertinibregressedanegfrmutantlungadenocarcinomabonemetastasismousemodelandincreasedlongtermsurvival
AT miwashinji osimertinibregressedanegfrmutantlungadenocarcinomabonemetastasismousemodelandincreasedlongtermsurvival
AT igarashikentaro osimertinibregressedanegfrmutantlungadenocarcinomabonemetastasismousemodelandincreasedlongtermsurvival
AT bouvetmichael osimertinibregressedanegfrmutantlungadenocarcinomabonemetastasismousemodelandincreasedlongtermsurvival
AT singhshreeram osimertinibregressedanegfrmutantlungadenocarcinomabonemetastasismousemodelandincreasedlongtermsurvival
AT tsuchiyahiroyuki osimertinibregressedanegfrmutantlungadenocarcinomabonemetastasismousemodelandincreasedlongtermsurvival
AT hoffmanrobertm osimertinibregressedanegfrmutantlungadenocarcinomabonemetastasismousemodelandincreasedlongtermsurvival