siRNA-Conjugated Nanoparticles to Treat Ovarian Cancer

SLAS Technol. 2019 Apr;24(2):137-150. doi: 10.1177/2472630318816668. Epub 2019 Jan 7.

Abstract

Ovarian cancer is the fifth-most lethal cancer among women due to a lack of early detection and late-stage treatment options, and it is responsible for more than 14,000 deaths each year in the United States. Recently, there have been advances in RNA interference therapy, specifically with small interfering RNA (siRNA), to reduce tumor burden for ovarian cancer via gene down-regulation. However, delivery of siRNA poses its own challenges, as siRNA is unstable in circulation, is unable to be effectively internalized by cells, and may cause toxicity in off-target sites. To address such challenges, nanoparticle carriers have emerged as delivery platforms for the biocompatible, targeted delivery of siRNA-based therapies. Several preclinical studies have shown the promising effects of siRNA therapy to reduce chemotherapy resistance and proliferation of ovarian cancer cells. This review evaluates the recent advances, clinical applications, and future potential of nanoparticle-mediated delivery of siRNA therapeutics to target genes implicated in ovarian cancer.

Keywords: gene therapy; nanotechnology; ovarian cancer; siRNA; targeting.

Publication types

  • Review

MeSH terms

  • Antineoplastic Agents / administration & dosage*
  • Biological Products / administration & dosage
  • Drug Carriers / administration & dosage*
  • Drug Evaluation, Preclinical
  • Female
  • Gene Knockdown Techniques
  • Gene Silencing
  • Humans
  • Molecular Targeted Therapy / methods*
  • Nanoparticles / administration & dosage*
  • Ovarian Neoplasms / therapy*
  • RNA, Small Interfering / administration & dosage*

Substances

  • Antineoplastic Agents
  • Biological Products
  • Drug Carriers
  • RNA, Small Interfering