Exploring Urtica dioica L. as a Promising Alternative Therapy for Obesity-Related Breast Cancer: Insights from
Ayla Eren1,2, Mehmet Varol1, Resat Unal1
1Department of Molecular Biology and Genetics, Faculty of Science, Muğla Sıtkı Koçman University, 48000, Kötekli, Muğla, Turkey.
Abstract:
Obesity and obesity-related breast cancer are major health problems that require alternative treatment strategies. Urtica dioica L. (U. dioica) stands out as a potential therapeutic candidate with its anti-oxidant, anti-cancer and lipid-lowering properties. In this study, the molecular effects of U. dioica were investigated by gene expression analysis and molecular docking methods. U. dioica significantly suppressed the expression of Brca1, Brca2, Fas, Lpl, Dgat1 and Mcp1 genes, resulting in significant changes in lipid metabolism, cancer susceptibility and inflammation. Molecular docking analyses showed that U. dioica components have strong binding affinities with target proteins. In particular, the interactions between Dgat1-Isorhamnetin rutinoside (-10.3 kcal/mol), Fas-Quercetin acetyl rutinoside (-10.3 kcal/mol), Lpl-Apigenin hexoside (-9.2 kcal/mol) and Mcp1-Quercetin acetyl rutinoside (-8.6 kcal/mol) were notable. In vitro and in silico analyses supported each other, revealing the effects of U. dioica in gene expression regulation and the potential for its constituents to interact with proteins. These findings indicate that U. dioica may be a promising alternative therapeutic agent in the treatment of obesity and obesity-related breast cancer and emphasize that its efficacy should be confirmed by clinical trials.
Insights
Urtica dioica L. (U. dioica) shows potential for treating obesity and related breast cancer by regulating genes involved in lipid metabolism, cancer, and inflammation. Its compounds effectively interact with target proteins, suggesting therapeutic promise.
Area of Science:
- Phytochemistry
- Molecular Biology
- Bioinformatics
Background:
- Obesity and associated breast cancer present significant global health challenges.
- Current treatments necessitate exploration of alternative therapeutic strategies.
- Urtica dioica L. (U. dioica) exhibits antioxidant, anticancer, and lipid-lowering properties, positioning it as a potential therapeutic agent.
Purpose of the Study:
- To investigate the molecular mechanisms underlying the effects of U. dioica.
- To evaluate the impact of U. dioica on gene expression related to lipid metabolism, cancer susceptibility, and inflammation.
- To assess the binding affinities of U. dioica components with target proteins using molecular docking.
Main Methods:
- Gene expression analysis was performed to determine the molecular effects of U. dioica.
- In silico molecular docking studies were conducted to predict interactions between U. dioica constituents and target proteins.
- In vitro and in silico approaches were integrated to validate findings.
Main Results:
- U. dioica significantly suppressed the expression of key genes including Brca1, Brca2, Fas, Lpl, Dgat1, and Mcp1.
- Significant alterations in lipid metabolism, cancer susceptibility, and inflammatory pathways were observed.
- Molecular docking revealed strong binding affinities between U. dioica compounds (e.g., Isorhamnetin rutinoside, Quercetin acetyl rutinoside, Apigenin hexoside) and target proteins (Dgat1, Fas, Lpl, Mcp1).
Conclusions:
- U. dioica demonstrates significant gene expression regulatory effects relevant to obesity and breast cancer.
- Its constituents show potential for targeted protein interactions, supporting its therapeutic efficacy.
- U. dioica emerges as a promising candidate for alternative treatments, warranting further clinical investigation.
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