一种含有开链聚醚的新型两亲角鲨烯基化合物可在体外和体内减少恶性黑色素瘤的转移

IF 8.2 2区 生物学 Q1 CELL BIOLOGY
Yaman Zhang, Meriem Bejaoui, Tran Ngoc Linh, Takashi Arimura, Hiroko Isoda
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引用次数: 0

摘要

角鲨烯(Squalene,SQ)是一种众所周知的抗氧化剂和消炎剂,对人体皮肤具有抗衰老和保护紫外线的作用。然而,由于角鲨烯具有较强的疏水性,同时还存在溶解性差、组织渗透性有限等问题,这给科学家们研究其在癌症进展等更复杂情况下尚未开发的潜力带来了挑战。本研究评估了一种新合成的两亲性乙二醇 SQ 衍生物(SQ-diEG)在黑色素瘤(最致命的皮肤癌)中的强效抗转移特性。体外和体内实验发现,SQ-diEG 可通过线粒体介导的 caspase 激活凋亡信号通路对黑色素瘤恶性肿瘤发挥潜能。在体外使用高增殖性和侵袭性黑色素瘤细胞观察到了 SQ-diEG 的强效抗转移作用。在 B16F10 肺定植小鼠模型中,服用 SQ-diEG(25 mg/kg)可明显减轻肺部肿瘤负荷,抑制转移相关蛋白和基因标记物。此外,全局基因谱分析也揭示了 SQ-diEG 在肿瘤微环境中的作用。我们预计,含有乙二醇低聚物的 SQ 化合物的两亲性可能会增强其到达病理部位的能力,从而提高其对黑色素瘤的治疗潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A novel amphiphilic squalene-based compound with open-chain polyethers reduces malignant melanoma metastasis in-vitro and in-vivo
Squalene (SQ) is a well-known antioxidant and anti-inflammatory agent that provides promising anti-aging and UV-protective roles on human skin. However, its strong hydrophobic nature, accompanied by issues such as poor solubility and limited tissue permeation, has created challenges for scientists to investigate its untapped potential in more complex conditions, including cancer progression. The present study assessed the potent anti-metastatic properties of a newly synthesized amphiphilic ethylene glycol SQ derivative (SQ-diEG) in melanoma, the most fatal skin cancer. In vitro and in vivo experiments have discovered that SQ-diEG may exert its potential on melanoma malignancy through the mitochondria-mediated caspase activation apoptotic signaling pathway. The potent anti-metastatic effect of SQ-diEG was observed in vitro using highly proliferative and aggressive melanoma cells. Administration of SQ-diEG (25 mg/kg) significantly decreased the tumor burden on the lung and inhibited the metastasis-associated proteins and gene markers in B16F10 lung colonization mice model. Furthermore, global gene profiling also revealed a promising role of SQ-diEG in tumor microenvironment. We anticipated that the amphiphilic nature of the SQ compound bearing ethylene glycol oligomers could potentially augment its ability to reach the pathology site, thus enhancing its therapeutic potential in melanoma.
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来源期刊
CiteScore
11.00
自引率
0.00%
发文量
180
期刊介绍: Cell Communication and Signaling (CCS) is a peer-reviewed, open-access scientific journal that focuses on cellular signaling pathways in both normal and pathological conditions. It publishes original research, reviews, and commentaries, welcoming studies that utilize molecular, morphological, biochemical, structural, and cell biology approaches. CCS also encourages interdisciplinary work and innovative models, including in silico, in vitro, and in vivo approaches, to facilitate investigations of cell signaling pathways, networks, and behavior. Starting from January 2019, CCS is proud to announce its affiliation with the International Cell Death Society. The journal now encourages submissions covering all aspects of cell death, including apoptotic and non-apoptotic mechanisms, cell death in model systems, autophagy, clearance of dying cells, and the immunological and pathological consequences of dying cells in the tissue microenvironment.
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