Glycyrrhizic acid-based multifunctional nanoplatform for tumor microenvironment regulation

Chin J Nat Med. 2024 Dec;22(12):1089-1099. doi: 10.1016/S1875-5364(24)60685-0.

Abstract

Natural compounds demonstrate unique therapeutic advantages for cancer treatment, primarily through direct tumor suppression or interference with the tumor microenvironment (TME). Glycyrrhizic acid (GL), a bioactive ingredient derived from the medicinal herb Glycyrrhiza uralensis Fisch., and its sapogenin glycyrrhetinic acid (GA), have been recognized for their ability to inhibit angiogenesis and remodel the TME. Consequently, the combination of GL with other therapeutic agents offers superior therapeutic benefits. Given GL's amphiphilic structure, self-assembly capability, and liver cancer targeting capacity, various GL-based nanoscale drug delivery systems have been developed. These GL-based nanosystems exhibit angiogenesis suppression and TME regulation properties, synergistically enhancing anti-cancer effects. This review summarizes recent advances in GL-based nanosystems, including polymer-drug micelles, drug-drug assembly nanoparticles (NPs), liposomes, and nanogels, for cancer treatment and tumor postoperative care, providing new insights into the anti-cancer potential of natural compounds. Additionally, the review discusses existing challenges and future perspectives for translating GL-based nanosystems from bench to bedside.

Keywords: Angiogenesis; Glycyrrhizic acid; Nanosystem; Self-assembly; Tumor microenvironment.

Publication types

  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacology
  • Antineoplastic Agents / therapeutic use
  • Drug Delivery Systems
  • Glycyrrhizic Acid* / chemistry
  • Glycyrrhizic Acid* / pharmacology
  • Glycyrrhizic Acid* / therapeutic use
  • Humans
  • Liposomes / chemistry
  • Micelles
  • Nanoparticles* / chemistry
  • Neoplasms* / drug therapy
  • Tumor Microenvironment* / drug effects

Substances

  • Glycyrrhizic Acid
  • Liposomes
  • Antineoplastic Agents
  • Micelles