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.

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.