4.2 Article

Simvastatin-loaded liposome nanoparticles treatment for uterine leiomyoma in a patient-derived xenograft mouse model: a pilot study

Journal

JOURNAL OF OBSTETRICS AND GYNAECOLOGY
Volume 42, Issue 6, Pages 2139-2143

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/01443615.2022.2033964

Keywords

Uterine leiomyoma; fibroid; simvastatin; nanoparticles; animal model

Funding

  1. NIH [1R01HD094380]
  2. Institute for Translational Sciences at the University of Texas Medical Branch
  3. Eunice Kennedy Shriver National Institute of Child Health and Human Development
  4. NIH NCATS [CTSA UL1TR000071]

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Simvastatin showed promising effects in treating leiomyomas, but simvastatin-loaded liposomal nanoparticles did not significantly improve the efficacy. Further research is needed to optimize the formulation of nanoparticles for sustainable delivery of simvastatin.
Uterine leiomyomas are complex tumours with limited medical treatment options. Simvastatin is used to treat hypercholesterolaemia and has shown promising effects as a treatment option for leiomyomas. Previously, our group demonstrated a promising effect of simvastatin treatment in a patient-derived xenograft mouse model. Here, we tested the efficacy of simvastatin liposomal nanoparticles (NPs). After bilateral leiomyoma xenograft implantation, mice (N = 12) were divided into three treatment arms: control, simvastatin and simvastatin-loaded liposome NPs (simvastatin-NPs). Treatment with simvastatin significantly reduced tumour volume and inhibited the Ki67 expression when compared to the control group. There was a trend of reduced tumour volume and Ki67 expression after treatment with simvastatin-NP; however, the results were not significant. Due to low bioavailability and short half-life of simvastatin, liposomal NPs have the potential to enhance drug delivery, however, in this study NP did not provide improvement over simvastatin, but did demonstrate their potential for the delivery of simvastatin.Impact statement What is already known on this subject? Simvastatin treatment in a patient-derived xenograft mouse model reduced tumour growth and decreased proliferation. What do the results of this study add? Treatment with simvastatin significantly reduced tumour volume and inhibited the Ki67 expression when compared to the control group. There was a trend of reduced tumour volume and Ki67 expression after treatment with simvastatin-NP, however, it did not improve the efficacy of simvastatin at reducing tumour growth and proliferation. What are the implications of these findings for clinical practice and/or further research? More studies are needed to optimise the formulation of NPs to further enhance the sustainable delivery of simvastatin.

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