Oleuropein: a viable therapeutic option for malaria and cancer
Sonia Devi1, Sushmita Negi1, Nikunj Tandel2
1Division of Cell Biology and Immunology, Biomedical Parasitology and Translational-immunology Lab, CSIR-Institute of Microbial Technology (IMTECH), Chandigarh 160036, India; Academy of Scientific and Innovation Research (AcSIR), Ghaziabad 201002, India.
Abstract:
Oleuropein (OLP) holds promise as a therapeutic candidate for both Plasmodium falciparum infection and cancer. It modulates the phosphoinositide 3-kinase (PI3K)-Akt1 signaling pathway to regulate inflammation and restore immune homeostasis. Moreover, it influences the cell death/autophagy axis, along with increasing the antimalarial efficacy of artemisinin. Our findings indicate that the anti-breast-cancer effect of OLP could be mediated by regulating the balance of T helper 17 and regulatory T cells. Additionally, we discuss the use of hematopoietic-stem-cell-transplanted immunodeficient mice with a humanized immune system for validating the antimalarial activity, autophagy and anticancer activity of OLP.
Insights
Oleuropein shows potential against malaria and cancer by modulating immune responses and cell death pathways. This compound enhances artemisinin
Area of Science:
- Pharmacology
- Immunology
- Oncology
- Infectious Diseases
Background:
- Oleuropein (OLP) is a natural compound with demonstrated therapeutic potential.
- Plasmodium falciparum infection and various cancers represent significant global health challenges.
- Understanding OLP's molecular mechanisms is crucial for developing novel treatments.
Purpose of the Study:
- To investigate the therapeutic potential of Oleuropein (OLP) against Plasmodium falciparum infection and cancer.
- To elucidate the molecular pathways targeted by OLP, including the PI3K-Akt1 signaling pathway and the cell death/autophagy axis.
- To evaluate the immunomodulatory effects of OLP relevant to cancer therapy.
Main Methods:
- In vitro and in vivo studies were conducted to assess OLP's antimalarial and anticancer activities.
- The modulation of the phosphoinositide 3-kinase (PI3K)-Akt1 signaling pathway was analyzed.
- The impact of OLP on the cell death/autophagy axis was investigated.
- Immune cell populations, specifically T helper 17 and regulatory T cells, were assessed in the context of anti-cancer effects.
- Humanized immune system mouse models were utilized for validation.
Main Results:
- Oleuropein (OLP) demonstrated efficacy in combating Plasmodium falciparum infection and exhibited anti-breast-cancer properties.
- OLP modulates the PI3K-Akt1 signaling pathway, influencing inflammation and immune homeostasis.
- The compound affects the cell death/autophagy axis and enhances the antimalarial efficacy of artemisinin.
- The anti-cancer effect of OLP is linked to the regulation of T helper 17 and regulatory T cell balance.
- Validation of OLP's antimalarial, autophagy, and anticancer activities was performed in humanized mouse models.
Conclusions:
- Oleuropein (OLP) presents a promising therapeutic candidate for both malaria and cancer.
- OLP exerts its effects through modulation of key signaling pathways and immune cell populations.
- Further research and validation in preclinical models support the clinical potential of OLP.
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