Fe3O4 nanoparticles containing gambogic acid inhibit metastasis in colorectal cancer via the RORB/EMILIN1 axis.

IF 3.3 3区 生物学 Q3 CELL BIOLOGY
Cell Adhesion & Migration Pub Date : 2024-12-01 Epub Date: 2024-11-13 DOI:10.1080/19336918.2024.2427585
Xiaodong Fan, Chunyang Lv, Meiling Xue, Peng Meng, Xiaoping Qian
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引用次数: 0

Abstract

This research aims to study the effect of magnetic nanoparticles of Fe3O4 (MNP Fe3O4) containing gambogic acid (GA-MNP Fe3O4) on colorectal cancer (CRC). MNP Fe3O4 enhanced the antitumor effect of GA by inhibiting the malignant behavior of CRC cells. RORB was a target of GA, and GA activated RORB expression to inhibit metastasis of CRC. Knockdown of RORB impaired the effect of GA-MNP Fe3O4 on CRC metastasis. EMILIN1 was a target of RORB, and RORB promoted transcription of EMILIN1. Overexpression of EMILIN1 reversed the effect of knockdown of RORB on GA-MNP Fe3O4 and inhibited metastasis in CRC. These findings revealed that MNP Fe3O4 enhanced the antitumor effect of GA and activated RORB to promote EMILIN1 transcription and inhibit CRC metastasis.

含有甘草酸的Fe3O4纳米粒子通过RORB/EMILIN1轴抑制结直肠癌转移
本研究旨在探讨含有甘草酸的磁性纳米颗粒Fe3O4(MNP Fe3O4)(GA-MNP Fe3O4)对结直肠癌(CRC)的影响。MNP Fe3O4通过抑制CRC细胞的恶性行为增强了GA的抗肿瘤作用。RORB是GA的靶点,GA激活RORB的表达以抑制CRC的转移。敲除RORB会削弱GA-MNP Fe3O4对CRC转移的影响。EMILIN1是RORB的靶标,RORB促进EMILIN1的转录。EMILIN1的过表达逆转了RORB敲除对GA-MNP Fe3O4的影响,并抑制了CRC的转移。这些研究结果表明,MNP Fe3O4增强了GA的抗肿瘤作用,并激活了RORB,促进了EMILIN1的转录,抑制了CRC的转移。
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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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