Fibronectin-containing High-Density Lipoprotein is Associated with Cancer Cell Adhesion and Proliferation.

Q3 Medicine Kobe Journal of Medical Sciences Pub Date : 2020-08-17
Eriko Hisamatsu, Manabu Nagao, Ryuji Toh, Yasuhiro Irino, Takuya Iino, Tetsuya Hara, Hidekazu Tanaka, Seimi Satomi-Kobayashi, Tatsuro Ishida, Ken-Ichi Hirata
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Abstract

A large amount of evidence suggests that high-density lipoprotein (HDL) has anti-atherosclerotic properties. HDL-cholesterol (HDL-C) has also been widely used as a marker of cardiovascular disease. Recently, it was reported that plasma HDL-C levels are inversely correlated with cancer risk. However, the relationship between HDL and cancer pathophysiology remains unknown. Here, we sought to investigate the effect of HDL on cancer progression. First, we focused on fibronectin-an essential extracellular matrix glycoprotein-as an HDL-associated protein and found that only 7.4% of subjects in this study had fibronectin in HDL isolated from their plasma. The fibronectin-containing HDL (FN-HDL) increased the phosphorylation of focal adhesion kinase (FAK) in HeLa cells compared to HDL without fibronectin, further inducing the phosphorylation in a dose-dependent manner. Second, we found that fibronectin-treated HDL activated the phosphorylation of FAK, and its upstream effector blocked the phosphorylation induced by FN-HDL. Finally, we demonstrated that FN-HDL promoted cancer cell proliferation and adhesion compared to HDL without fibronectin. Our study showed the possible mechanism by which FN-HDL enhanced cancer cell proliferation and adhesion via the FAK signaling pathway. Further investigation of the roles of HDL components in tumorigenesis might provide novel insight into cancer pathophysiology.

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含纤维连接蛋白的高密度脂蛋白与癌细胞粘附和增殖有关。
大量证据表明高密度脂蛋白(HDL)具有抗动脉粥样硬化的特性。高密度脂蛋白胆固醇(HDL-C)也被广泛用作心血管疾病的标志物。最近,有报道称血浆HDL-C水平与癌症风险呈负相关。然而,HDL与癌症病理生理之间的关系尚不清楚。在这里,我们试图研究HDL对癌症进展的影响。首先,我们关注纤维连接蛋白——一种必需的细胞外基质糖蛋白——作为HDL相关蛋白,发现在本研究中只有7.4%的受试者从血浆中分离出HDL中的纤维连接蛋白。与不含纤维连接蛋白的HDL相比,含纤维连接蛋白的HDL (FN-HDL)增加了HeLa细胞中局灶黏附激酶(FAK)的磷酸化,并以剂量依赖性的方式进一步诱导磷酸化。其次,我们发现纤维连接蛋白处理的HDL激活了FAK的磷酸化,其上游效应物阻断了FN-HDL诱导的磷酸化。最后,我们证明了与不含纤维连接蛋白的HDL相比,FN-HDL促进了癌细胞的增殖和粘附。我们的研究揭示了FN-HDL通过FAK信号通路增强癌细胞增殖和粘附的可能机制。进一步研究HDL成分在肿瘤发生中的作用可能为癌症病理生理学提供新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Kobe Journal of Medical Sciences
Kobe Journal of Medical Sciences Medicine-Medicine (all)
CiteScore
1.20
自引率
0.00%
发文量
4
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