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FGFR inhibitors combined with nab-paclitaxel - A promising strategy to treat non-small cell lung cancer and overcome resistance

Lung cancer has high morbidity and mortality rates worldwide, and NSCLC accounts for 85% of all lung cancer cases. Despite the development of targeted therapies and immunotherapy, many NSCLC patients do not effectively respond to treatment, and new treatment strategies are urgently needed. Aberrant...

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Autores principales: Ma, Feng, Zhu, Xinhai, Niu, Yuchun, Nai, Aitao, Bashir, Shoaib, Xiong, Yan, Dong, Yunlong, Li, Yin, Song, Jian, Xu, Meng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9950728/
https://www.ncbi.nlm.nih.gov/pubmed/36845692
http://dx.doi.org/10.3389/fonc.2023.1088444
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author Ma, Feng
Zhu, Xinhai
Niu, Yuchun
Nai, Aitao
Bashir, Shoaib
Xiong, Yan
Dong, Yunlong
Li, Yin
Song, Jian
Xu, Meng
author_facet Ma, Feng
Zhu, Xinhai
Niu, Yuchun
Nai, Aitao
Bashir, Shoaib
Xiong, Yan
Dong, Yunlong
Li, Yin
Song, Jian
Xu, Meng
author_sort Ma, Feng
collection PubMed
description Lung cancer has high morbidity and mortality rates worldwide, and NSCLC accounts for 85% of all lung cancer cases. Despite the development of targeted therapies and immunotherapy, many NSCLC patients do not effectively respond to treatment, and new treatment strategies are urgently needed. Aberrant activation of the FGFR signaling pathway is closely related to the initiation and progression of tumors. AZD4547, which is a selective inhibitor of FGFR 1-3, can suppress the growth of tumor cells with deregulated FGFR expression in vivo and in vitro. However, further exploration is needed to determine whether AZD4547 can play an antiproliferative role in tumor cells without deregulated FGFR expression. We investigated the antiproliferative effect of AZD4547 on NSCLC cells without deregulated FGFR expression. In vivo and in vitro experiments showed that AZD4547 exerted a weak antiproliferative effect on NSCLC cells without deregulated FGFR expression, but it significantly enhanced the sensitivity of NSCLC cells to nab-paclitaxel. We found that AZD4547 combined with nab-paclitaxel suppressed the phosphorylation of the MAPK signaling pathway, led to cell cycle arrest in the G2/M phase, promoted apoptosis, and inhibited cell proliferation more substantially than nab-paclitaxel alone. These findings provide insight into the rational use of FGFR inhibitors and personalized treatment of NSCLC patients.
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spelling pubmed-99507282023-02-25 FGFR inhibitors combined with nab-paclitaxel - A promising strategy to treat non-small cell lung cancer and overcome resistance Ma, Feng Zhu, Xinhai Niu, Yuchun Nai, Aitao Bashir, Shoaib Xiong, Yan Dong, Yunlong Li, Yin Song, Jian Xu, Meng Front Oncol Oncology Lung cancer has high morbidity and mortality rates worldwide, and NSCLC accounts for 85% of all lung cancer cases. Despite the development of targeted therapies and immunotherapy, many NSCLC patients do not effectively respond to treatment, and new treatment strategies are urgently needed. Aberrant activation of the FGFR signaling pathway is closely related to the initiation and progression of tumors. AZD4547, which is a selective inhibitor of FGFR 1-3, can suppress the growth of tumor cells with deregulated FGFR expression in vivo and in vitro. However, further exploration is needed to determine whether AZD4547 can play an antiproliferative role in tumor cells without deregulated FGFR expression. We investigated the antiproliferative effect of AZD4547 on NSCLC cells without deregulated FGFR expression. In vivo and in vitro experiments showed that AZD4547 exerted a weak antiproliferative effect on NSCLC cells without deregulated FGFR expression, but it significantly enhanced the sensitivity of NSCLC cells to nab-paclitaxel. We found that AZD4547 combined with nab-paclitaxel suppressed the phosphorylation of the MAPK signaling pathway, led to cell cycle arrest in the G2/M phase, promoted apoptosis, and inhibited cell proliferation more substantially than nab-paclitaxel alone. These findings provide insight into the rational use of FGFR inhibitors and personalized treatment of NSCLC patients. Frontiers Media S.A. 2023-02-10 /pmc/articles/PMC9950728/ /pubmed/36845692 http://dx.doi.org/10.3389/fonc.2023.1088444 Text en Copyright © 2023 Ma, Zhu, Niu, Nai, Bashir, Xiong, Dong, Li, Song and Xu 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
Ma, Feng
Zhu, Xinhai
Niu, Yuchun
Nai, Aitao
Bashir, Shoaib
Xiong, Yan
Dong, Yunlong
Li, Yin
Song, Jian
Xu, Meng
FGFR inhibitors combined with nab-paclitaxel - A promising strategy to treat non-small cell lung cancer and overcome resistance
title FGFR inhibitors combined with nab-paclitaxel - A promising strategy to treat non-small cell lung cancer and overcome resistance
title_full FGFR inhibitors combined with nab-paclitaxel - A promising strategy to treat non-small cell lung cancer and overcome resistance
title_fullStr FGFR inhibitors combined with nab-paclitaxel - A promising strategy to treat non-small cell lung cancer and overcome resistance
title_full_unstemmed FGFR inhibitors combined with nab-paclitaxel - A promising strategy to treat non-small cell lung cancer and overcome resistance
title_short FGFR inhibitors combined with nab-paclitaxel - A promising strategy to treat non-small cell lung cancer and overcome resistance
title_sort fgfr inhibitors combined with nab-paclitaxel - a promising strategy to treat non-small cell lung cancer and overcome resistance
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9950728/
https://www.ncbi.nlm.nih.gov/pubmed/36845692
http://dx.doi.org/10.3389/fonc.2023.1088444
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