Fibronectin-containing High-Density Lipoprotein is Associated with Cancer Cell Adhesion and Proliferation.
Adult
Aged
Biomarkers, Tumor
/ metabolism
Carcinogenesis
/ metabolism
Cell Adhesion
/ physiology
Cell Proliferation
/ physiology
Disease Progression
Female
Fibronectins
/ metabolism
Focal Adhesion Protein-Tyrosine Kinases
/ metabolism
HeLa Cells
Humans
Lipoproteins, HDL
/ metabolism
Male
Middle Aged
Phosphorylation
Signal Transduction
Cancer progression
Fibronectin
Focal Adhesion Kinase
High-density lipoprotein
Journal
The Kobe journal of medical sciences
ISSN: 1883-0498
Titre abrégé: Kobe J Med Sci
Pays: Japan
ID NLM: 0413531
Informations de publication
Date de publication:
17 Aug 2020
17 Aug 2020
Historique:
entrez:
21
8
2020
pubmed:
21
8
2020
medline:
21
7
2021
Statut:
epublish
Résumé
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.
Substances chimiques
Biomarkers, Tumor
0
Fibronectins
0
Lipoproteins, HDL
0
Focal Adhesion Protein-Tyrosine Kinases
EC 2.7.10.2
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
E40-E48Références
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