Disintegrin-like Protein Strategy to Inhibit Aggressive Triple-Negative Breast Cancer.
Inès LimamMohamed AbdelkarimMohamed El AyebMichel CrepinNaziha MarrakchiMélanie Di BenedettoPublished in: International journal of molecular sciences (2023)
Venoms are a rich source of bioactive compounds, and among them is leberagin-C (Leb-C), a disintegrin-like protein derived from the venom of Macrovipera lebetina transmediterrannea snakes. Leb-C has shown promising inhibitory effects on platelet aggregation. Previous studies have demonstrated that this SECD protein specifically targets α5β1, αvβ3, and αvβ6 integrins through a mimic mechanism of RGD disintegrins. In our current study, we focused on exploring the potential effects of Leb-C on metastatic breast cancer. Our findings revealed that Leb-C disrupted the adhesion, migration, and invasion capabilities of MDA-MB-231 breast cancer cells and its highly metastatic D3H2LN sub-population. Additionally, we observed significant suppression of adhesion, migration, and invasion of human umbilical vein endothelial cells (HUVECs). Furthermore, Leb-C demonstrated a strong inhibitory effect on fibroblast-growth-factor-2-induced proliferation of HUVEC. We conducted in vivo experiments using nude mice and found that treatment with 2 µM of Leb-C resulted in a remarkable 73% reduction in D3H2LN xenograft tumor size. Additionally, quantification of intratumor microvessels revealed a 50% reduction in tumor angiogenesis in xenograft after 21 days of twice-weekly treatment with 2 µM of Leb-C. Collectively, these findings suggest the potential utility of this disintegrin-like protein for inhibiting aggressive and resistant metastatic breast cancer.
Keyphrases
- metastatic breast cancer
- endothelial cells
- breast cancer cells
- high glucose
- signaling pathway
- squamous cell carcinoma
- small cell lung cancer
- escherichia coli
- single cell
- vascular endothelial growth factor
- oxidative stress
- biofilm formation
- skeletal muscle
- adipose tissue
- type diabetes
- pseudomonas aeruginosa
- functional connectivity
- replacement therapy
- combination therapy
- candida albicans
- cell adhesion