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成纤维细胞生长因子受体(FGFR)抑制剂联合白蛋白结合型紫杉醇——一种治疗非小细胞肺癌和克服耐药性的有前景的策略。

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

作者信息

Ma Feng, Zhu Xinhai, Niu Yuchun, Nai Aitao, Bashir Shoaib, Xiong Yan, Dong Yunlong, Li Yin, Song Jian, Xu Meng

机构信息

Department of Oncology, The First Affiliated Hospital of Jinan University, Jinan University, Guangzhou, China.

Department of Oncology, The First Affiliated Hospital of Hebei North University, Zhangjiakou, China.

出版信息

Front Oncol. 2023 Feb 10;13:1088444. doi: 10.3389/fonc.2023.1088444. eCollection 2023.

DOI:10.3389/fonc.2023.1088444
PMID:36845692
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9950728/
Abstract

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 and . 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. and 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.

摘要

肺癌在全球范围内具有较高的发病率和死亡率,非小细胞肺癌(NSCLC)占所有肺癌病例的85%。尽管靶向治疗和免疫治疗有所发展,但许多NSCLC患者对治疗没有有效的反应,迫切需要新的治疗策略。FGFR信号通路的异常激活与肿瘤的发生和发展密切相关。AZD4547是一种FGFR 1 - 3的选择性抑制剂,可抑制FGFR表达失调的肿瘤细胞的生长。然而,需要进一步探索AZD4547在FGFR表达未失调的肿瘤细胞中是否能发挥抗增殖作用。我们研究了AZD4547对FGFR表达未失调的NSCLC细胞的抗增殖作用。实验表明,AZD4547对FGFR表达未失调的NSCLC细胞具有较弱的抗增殖作用,但它显著增强了NSCLC细胞对白蛋白结合型紫杉醇的敏感性。我们发现,AZD4547与白蛋白结合型紫杉醇联合使用可抑制MAPK信号通路的磷酸化,导致细胞周期停滞在G2/M期,促进细胞凋亡,并且比单独使用白蛋白结合型紫杉醇更能显著抑制细胞增殖。这些发现为FGFR抑制剂的合理使用和NSCLC患者的个性化治疗提供了思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/731b/9950728/f83962e4e53b/fonc-13-1088444-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/731b/9950728/aadca172db88/fonc-13-1088444-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/731b/9950728/f83962e4e53b/fonc-13-1088444-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/731b/9950728/aadca172db88/fonc-13-1088444-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/731b/9950728/7a1312a7bd7e/fonc-13-1088444-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/731b/9950728/45579a9d4401/fonc-13-1088444-g003.jpg
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