NaV1.5 和 Rac1 对乳腺癌上皮-间质转化的影响

IF 1.8 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Zhuocen Zha, Fei Ge, Na Li, Shijun Zhang, Chenxi Wang, Fuhong Gong, Jingge Miao, Wenlin Chen
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引用次数: 0

摘要

乳腺癌是一种严重危害妇女健康的疾病。然而,由于出现转移和耐药,治疗困难。探讨乳腺癌的转移机制有助于找到合适的靶点。上皮-间质转化(EMT)是乳腺癌转移的重要机制。钠通道1.5(NaV1.5)和GTPase Rac1是影响乳腺肿瘤恶性程度的因素。NaV1.5的表达和Rac1的激活都参与了EMT的发生。此外,NaV1.5可以通过促进Na+的流入改变细胞膜电位(Vm),使细胞膜去极化,诱导Rac1的激活,产生一系列反应,导致乳腺癌细胞EMT;这一系列事件进一步诱导肿瘤细胞的运动、迁移和侵袭,影响乳腺癌患者的预后。本文就NaV1.5和Rac1在emt介导的乳腺癌进展中的作用进行综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of NaV1.5 and Rac1 on the Epithelial-Mesenchymal Transition in Breast Cancer.

Breast cancer is a disease that seriously endangers the health of women. However, it is difficult to treat due to the emergence of metastasis and drug resistance. Exploring the metastasis mechanism of breast cancer is helpful to aim for the appropriate target. The epithelial-mesenchymal transition (EMT) is an important mechanism of breast cancer metastasis. Sodium channel 1.5(NaV1.5) and the GTPase Rac1 are factors related to the degree of malignancy of breast tumors. The expression of NaV1.5 and the activation of Rac1 are both involved in EMT. In addition, NaV1.5 can change the plasma membrane potential (Vm) by promoting the inflow of Na+ to depolarize the cell membrane, induce the activation of Rac1 and produce a cascade of reactions that lead to EMT in breast cancer cells; this sequence of events further induces the movement, migration and invasion of tumor cells and affects the prognosis of breast cancer patients. In this paper, the roles of NaV1.5 and Rac1 in EMT-mediated breast cancer progression were reviewed.

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来源期刊
Cell Biochemistry and Biophysics
Cell Biochemistry and Biophysics 生物-生化与分子生物学
CiteScore
4.40
自引率
0.00%
发文量
72
审稿时长
7.5 months
期刊介绍: Cell Biochemistry and Biophysics (CBB) aims to publish papers on the nature of the biochemical and biophysical mechanisms underlying the structure, control and function of cellular systems The reports should be within the framework of modern biochemistry and chemistry, biophysics and cell physiology, physics and engineering, molecular and structural biology. The relationship between molecular structure and function under investigation is emphasized. Examples of subject areas that CBB publishes are: · biochemical and biophysical aspects of cell structure and function; · interactions of cells and their molecular/macromolecular constituents; · innovative developments in genetic and biomolecular engineering; · computer-based analysis of tissues, cells, cell networks, organelles, and molecular/macromolecular assemblies; · photometric, spectroscopic, microscopic, mechanical, and electrical methodologies/techniques in analytical cytology, cytometry and innovative instrument design For articles that focus on computational aspects, authors should be clear about which docking and molecular dynamics algorithms or software packages are being used as well as details on the system parameterization, simulations conditions etc. In addition, docking calculations (virtual screening, QSAR, etc.) should be validated either by experimental studies or one or more reliable theoretical cross-validation methods.
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