Nanoquercetin and Extracellular Vesicles as Potential Anticancer Therapeutics in Hepatocellular Carcinoma

Alok Raghav1, Goo Bo Jeong1

  • 1Department of Anatomy and Cell Biology, College of Medicine, Gachon University, 155 Getbeol-ro, Yeonsu-gu, Incheon 21999, Republic of Korea.

Cells
|April 12, 2024
PubMed

Insights

Natural nanoquercetin delivered via extracellular vesicles shows promise for treating hepatocellular carcinoma by regulating key cancer pathways. This approach offers a potential alternative to conventional cancer therapies, reducing limitations and toxicities.

Area of Science:

  • Biotechnology
  • Nanomedicine
  • Oncology

Background:

  • Cancer mortality remains high despite advanced technologies.
  • Conventional drug therapies for cancer have significant limitations and toxicities.
  • Natural compounds like nanoquercetin offer potential alternative treatments.

Purpose of the Study:

  • To investigate the potential of extracellular vesicle (EV)-based nanoquercetin (nQ) delivery for hepatocellular carcinoma (HCC) treatment.
  • To explore the synergistic effects of EVs and nQ on cancer signaling pathways.
  • To understand the role of EVs in regulating microRNAs (miRNAs) for HCC therapy.

Main Methods:

  • Utilized extracellular vesicles (EVs) for targeted delivery of nanoquercetin (nQ).
  • Investigated the modulation of key signaling pathways including NF-κB, p53, JAK/STAT, MAPK, Wnt/β-catenin, and PI3K/AKT.
  • Analyzed the impact on PBX3/ERK1/2/CDK2 and miRNA expression in the context of HCC.

Main Results:

  • EVs-based nQ delivery demonstrated synergistic regulation and dysregulation of multiple cancer-associated signaling pathways.
  • Identified potential checkpoints within anticancer signaling pathways.
  • Demonstrated the governing role of EVs in controlling miRNA expression relevant to HCC.

Conclusions:

  • EVs-mediated targeted delivery of nQ presents a promising strategy for HCC treatment.
  • This approach offers a synergistic effect by modulating critical signaling pathways and miRNAs.
  • Further development of modified EVs with nQ could lead to innovative HCC therapies.