A Strategic Antimetastatic Solution for Bone-Targeting Prostate Cancer via Nanoengineered Niclosamide

Sanoj Rejinold N1, Geun-Woo Jin2, Jin-Ho Choy1,3

  • 1Intelligent Nanohybrid Materials Laboratory (INML), Department of Chemistry, College of Science and Technology, Dankook University, Cheonan 31116, Republic of Korea.

Nano Letters
|July 14, 2025
PubMed

Insights

Repurposing the drug niclosamide using nanotechnology may offer a new strategy to combat advanced prostate cancer and prevent its spread to bones. This approach targets cancer hallmarks to improve patient outcomes.

Area of Science:

  • Oncology
  • Nanotechnology
  • Drug Repurposing

Background:

  • Prostate cancer is a leading cause of male cancer deaths globally.
  • Skeletal metastasis significantly drives mortality in advanced prostate cancer.
  • Innovative therapies are crucial for managing bone metastasis and improving patient survival.

Purpose of the Study:

  • To explore the potential of nanotechnology-enabled niclosamide for treating metastatic prostate cancer.
  • To investigate the efficacy of niclosamide nanohybrids in suppressing tumor growth and bone dissemination.
  • To provide a molecular rationale and design considerations for nanoengineered niclosamide.

Main Methods:

  • Formulating niclosamide into smart, targeted nanohybrids.
  • Evaluating the anti-cancer properties of nanoengineered niclosamide.
  • Assessing the inhibition of prostate tumor growth and skeletal metastasis.

Main Results:

  • Niclosamide demonstrates multipathway modulation against cancer hallmarks.
  • Nanotechnology-based formulation enhances niclosamide's therapeutic potential.
  • Targeted nanohybrids show promise in suppressing tumor growth and metastasis.

Conclusions:

  • Nanoengineered niclosamide presents a promising therapeutic strategy for metastatic prostate cancer.
  • This approach could potentially inhibit skeletal metastasis and improve patient outcomes.
  • Further research and translational studies are warranted for clinical application.