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Chlorogenic Acid and Cinnamaldehyde in Combination Inhibit Metastatic Traits and Induce Apoptosis via Akt
Yusuff Olayiwola1, Lauren S Gollahon1
1Department of Biological Sciences, Texas Tech University, Lubbock, TX 79407, USA.
Abstract:
Most reported breast cancer-associated deaths are directly correlated with metastatic disease. Additionally, the primary goal of treating metastatic breast cancer is to prolong life. Thus, there remains the need for more effective and safer strategies to treat metastatic breast cancer. Recently, more attention has been given to natural products (or phytochemicals) as potential anticancer treatments. This study aimed to investigate the synergistic effects of the combination of the phytochemicals chlorogenic acid and cinnamaldehyde (CGA and CA) toward inhibiting metastasis. The hypothesis was that CGA and CA in combination decrease the metastatic potential of breast cancer cells by inhibiting their invasive and migratory abilities as well as the induction of apoptosis via the downregulation of the Akt, disrupting its signal transduction pathway. To test this, wound-healing and Transwell™ Matrigel™ assays were conducted to assess changes in the migration and invasion properties of the cells; apoptosis was analyzed by fluorescence microscopy for Annexin V/propidium iodide; and immunoblotting and FACSort were performed on markers for the epithelial-to-mesenchymal transition status. The results show that CGA and CA significantly downregulated Akt activation by inhibiting phosphorylation. Consequently, increased caspase 3 and decreased Bcl2-α levels were observed, and apoptosis was confirmed. The inhibition of metastatic behavior was demonstrated by the attenuation of N-cadherin, fibronectin, vimentin, and MMP-9 expressions with concomitant increased expressions of E-cadherin and EpCAM. In summary, the present study demonstrated that CGA and CA in combination downregulated Akt activation, inhibited the metastatic potential, and induced apoptosis in different breast cancer cell lines.
Insights
This study shows that combining chlorogenic acid (CGA) and cinnamaldehyde (CA) natural compounds can effectively inhibit breast cancer metastasis. These phytochemicals reduce cancer cell invasion and migration while promoting cell death.
Area of Science:
- Oncology
- Natural Products Chemistry
- Molecular Biology
Background:
- Metastatic breast cancer is a leading cause of cancer-related deaths, necessitating novel therapeutic strategies.
- Natural products, or phytochemicals, are gaining attention as potential anticancer agents.
- Targeting metastasis and inducing apoptosis are key goals in breast cancer treatment.
Purpose of the Study:
- To investigate the synergistic effects of chlorogenic acid (CGA) and cinnamaldehyde (CA) in inhibiting breast cancer metastasis.
- To determine if the combination of CGA and CA downregulates the Akt signaling pathway, affecting cell invasion, migration, and apoptosis.
- To evaluate the impact of CGA and CA on epithelial-to-mesenchymal transition (EMT) markers.
Main Methods:
- Wound-healing and Transwell™ Matrigel™ assays were used to assess cell migration and invasion.
- Apoptosis was analyzed using Annexin V/propidium iodide staining and fluorescence microscopy.
- Immunoblotting and FACSort were employed to evaluate EMT markers and Akt pathway activation (phosphorylation).
Main Results:
- CGA and CA significantly downregulated Akt activation by inhibiting phosphorylation.
- The combination treatment led to increased caspase 3 and decreased Bcl2-α levels, confirming apoptosis induction.
- Metastatic potential was inhibited, evidenced by decreased N-cadherin, fibronectin, vimentin, and MMP-9, and increased E-cadherin and EpCAM expression.
Conclusions:
- Chlorogenic acid and cinnamaldehyde act synergistically to inhibit breast cancer cell metastasis.
- The CGA and CA combination effectively downregulates the Akt signaling pathway, leading to reduced invasion and migration.
- This phytochemical combination induces apoptosis and reverses EMT, presenting a promising strategy for metastatic breast cancer treatment.
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