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经过动态超稀释的扰乱了质膜的组织,减少了黑色素瘤癌细胞的迁移。

Dynamized ultra-low dilution of disrupts plasma membrane organization and decreases migration of melanoma cancer cell.

机构信息

Center Armand-Frappier Santé Biotechnologie of the INRS, University of Quebec, Laval, Quebec, Canada.

CNRS UMR 7369 MEDyC, University of Reims Champagne-Ardenne, Reims, France.

出版信息

Cell Adh Migr. 2023 Dec;17(1):1-13. doi: 10.1080/19336918.2022.2154732.

DOI:10.1080/19336918.2022.2154732
PMID:36503402
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9746621/
Abstract

Cutaneous melanoma is a cancer with a very poor prognosis mainly because of metastatic dissemination and therefore a deregulation of cell migration. Current therapies can benefit from complementary medicines as supportive care in oncology. In our study, we show that a dynamized ultra-low dilution of leads to an inhibition of migration on fibronectin of B16F10 melanoma cells, as well as a decrease in metastatic dissemination . These effects appear to be due to a disruption of plasma membrane organization, with a change in cell and membrane stiffness, associated with a disorganization of the actin cytoskeleton and a modification of the lipid composition of the plasma membrane. Together, these results demonstrate, in and models of cutaneous melanoma, an anti-cancer and anti-metastatic activity of ultra-low dynamized dilution of and reinforce its interest as complementary medicine in oncology.

摘要

皮肤黑色素瘤是一种预后非常差的癌症,主要是因为转移和扩散,因此细胞迁移受到了调节。目前的治疗方法可以受益于补充药物作为肿瘤学的支持性护理。在我们的研究中,我们表明,经过动态超稀释处理的 leads 会抑制 B16F10 黑色素瘤细胞在纤维连接蛋白上的迁移,同时减少转移性扩散。这些效果似乎是由于细胞膜组织的破坏,导致细胞和细胞膜硬度的变化,伴随着肌动蛋白细胞骨架的紊乱和质膜脂质组成的改变。总之,这些结果表明,在皮肤黑色素瘤的和 模型中,超动态稀释的 具有抗癌和抗转移活性,并增强了其作为肿瘤学补充药物的应用价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc92/9746621/fab4c5982dea/KCAM_A_2154732_F0007_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc92/9746621/f0eb8635a6e1/KCAM_A_2154732_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc92/9746621/eed4d428509f/KCAM_A_2154732_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc92/9746621/ec212d16dee9/KCAM_A_2154732_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc92/9746621/e38ef508379d/KCAM_A_2154732_F0004_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc92/9746621/fd6796ada407/KCAM_A_2154732_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc92/9746621/eb00538c5e79/KCAM_A_2154732_F0006_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc92/9746621/fab4c5982dea/KCAM_A_2154732_F0007_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc92/9746621/f0eb8635a6e1/KCAM_A_2154732_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc92/9746621/eed4d428509f/KCAM_A_2154732_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc92/9746621/ec212d16dee9/KCAM_A_2154732_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc92/9746621/e38ef508379d/KCAM_A_2154732_F0004_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc92/9746621/fd6796ada407/KCAM_A_2154732_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc92/9746621/eb00538c5e79/KCAM_A_2154732_F0006_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc92/9746621/fab4c5982dea/KCAM_A_2154732_F0007_OC.jpg

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