FGFR1在FGFR1扩增的肺癌中通过靶向CCND1调控增殖和转移。

IF 3.3 3区 生物学 Q3 CELL BIOLOGY
Ying Yang, Tingting Lu, Ziming Li, Shun Lu
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引用次数: 23

摘要

目的:通过对在线数据库的分析,发现CCND1表达与LSCC预后不良相关。我们旨在探讨CCND1在LSCC肿瘤进展中的功能。主要方法:采用qRT-PCR法检测mRNA的表达。Western blot检测蛋白表达。transwell法检测细胞迁移和侵袭。关键发现:肺癌患者中CCND1与FGFR1共过表达。CCND1过表达促进LSCC细胞增殖和转移。FGFR1在FGFR1扩增细胞系中靶向CCND1,通过AKT/MAPK信号通路促进EMT过程。总之,我们的研究证明了CCND1和FGFR1在FGFR1扩增的LSCC中的调控机制。共同靶向CCND1和FGFR1可以提供更大的临床益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

FGFR1 regulates proliferation and metastasis by targeting CCND1 in FGFR1 amplified lung cancer.

FGFR1 regulates proliferation and metastasis by targeting CCND1 in FGFR1 amplified lung cancer.

FGFR1 regulates proliferation and metastasis by targeting CCND1 in FGFR1 amplified lung cancer.

FGFR1 regulates proliferation and metastasis by targeting CCND1 in FGFR1 amplified lung cancer.

Aims: The analysis of the online databases revealed that CCND1 expression is correlated with poor prognosis in LSCC. We aimed to explore the function of CCND1 in tumor progression in LSCC.Main methods: The expression of mRNA was measured using qRT-PCR. Protein expression was assessed by Western blot. Cell migration and invasion were assessed by transwell assay.Key findings: CCND1 was co-overexpressed with FGFR1 in lung cancer patients. Overexpression of CCND1 promoted LSCC cell proliferation and metastasis. FGFR1 promoted the processes of EMT through AKT/MAPK signaling by targeting CCND1 in FGFR1-amplification cell lines.Significance: IIn conclusion, our study demonstrated the regulatory mechanism between CCND1 and FGFR1 in FGFR1 amplified LSCC. Co-targeting CCND1 and FGFR1 could provide greater clinical benefits.

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来源期刊
CiteScore
6.40
自引率
0.00%
发文量
7
审稿时长
53 weeks
期刊介绍: Cell Adhesion & Migration is a multi-disciplinary, peer reviewed open access journal that focuses on the biological or pathological implications of cell-cell and cell-microenvironment interactions. The main focus of this journal is fundamental science. The journal strives to serve a broad readership by regularly publishing review articles covering specific disciplines within the field, and by publishing focused issues that provide an overview on specific topics of interest within the field. Cell Adhesion & Migration publishes relevant and timely original research, as well as authoritative overviews, commentaries, and perspectives, providing context for the work presented in Cell Adhesion & Migration and for key results published elsewhere. Original research papers may cover all topics important in the field of cell-cell and cell-matrix interactions. Cell Adhesion & Migration also publishes articles related to cell biomechanics, biomaterial, and development of related imaging technologies.
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