Maximizing arsenic trioxide's anticancer potential: Targeted nanocarriers for solid tumor therapy

Colloids Surf B Biointerfaces. 2024 Sep:241:114014. doi: 10.1016/j.colsurfb.2024.114014. Epub 2024 Jun 4.

Abstract

Arsenic trioxide (ATO) has gained significant attention due to its promising therapeutic effects in treating different diseases, particularly acute promyelocytic leukemia (APL). Its potent anticancer mechanisms have been extensively studied. Despite the great efficacy ATO shows in fighting cancers, drawbacks in the clinical use are obvious, especially for solid tumors, which include rapid renal clearance and short half-life, severe adverse effects, and high toxicity to normal cells. Recently, the emergence of nanomedicine offers a potential solution to these limitations. The enhanced biocompatibility, excellent targeting capability, and desirable effectiveness have attracted much interest. Therefore, we summarized various nanocarriers for targeted delivery of ATO to solid tumors. We also provided detailed anticancer mechanisms of ATO in treating cancers, its clinical trials and shortcomings as well as the combination therapy of ATO and other chemotherapeutic agents for reduced drug resistance and synergistic effects. Finally, the future study direction and prospects were also presented.

Keywords: Anticancer mechanisms; Arsenic trioxide; Combination therapy; Nanocarriers; Targeted drug delivery.

Publication types

  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents* / administration & dosage
  • Antineoplastic Agents* / chemistry
  • Antineoplastic Agents* / pharmacology
  • Arsenic Trioxide* / administration & dosage
  • Arsenic Trioxide* / chemistry
  • Arsenic Trioxide* / pharmacology
  • Drug Carriers* / chemistry
  • Drug Delivery Systems
  • Humans
  • Nanoparticles / chemistry
  • Neoplasms* / drug therapy

Substances

  • Arsenic Trioxide
  • Antineoplastic Agents
  • Drug Carriers