Marine-Derived Anticancer Agents Targeting Apoptotic Pathways: Exploring the Depths for Novel Cancer Therapies

Mar Drugs. 2024 Feb 28;22(3):114. doi: 10.3390/md22030114.

Abstract

Extensive research has been conducted on the isolation and study of bioactive compounds derived from marine sources. Several natural products have demonstrated potential as inducers of apoptosis and are currently under investigation in clinical trials. These marine-derived compounds selectively interact with extrinsic and intrinsic apoptotic pathways using a variety of molecular mechanisms, resulting in cell shrinkage, chromatin condensation, cytoplasmic blebs, apoptotic bodies, and phagocytosis by adjacent parenchymal cells, neoplastic cells, or macrophages. Numerous marine-derived compounds are currently undergoing rigorous examination for their potential application in cancer therapy. This review examines a total of 21 marine-derived compounds, along with their synthetic derivatives, sourced from marine organisms such as sponges, corals, tunicates, mollusks, ascidians, algae, cyanobacteria, fungi, and actinobacteria. These compounds are currently undergoing preclinical and clinical trials to evaluate their potential as apoptosis inducers for the treatment of different types of cancer. This review further examined the compound's properties and mode of action, preclinical investigations, clinical trial studies on single or combination therapy, and the prospective development of marine-derived anticancer therapies.

Keywords: anticancer; apoptotic agents; clinical trials; combination therapy; marine actinobacteria; marine natural products; marine sponges; mechanism of action.

Publication types

  • Review

MeSH terms

  • Actinobacteria*
  • Animals
  • Anthozoa*
  • Antineoplastic Agents*
  • Clinical Trials as Topic
  • Neoplasms*
  • Prospective Studies

Substances

  • Antineoplastic Agents

Grants and funding

This research was funded by the Department of Science and Technology, Philippine Council for Health Research and Development (DOST-PCHRD) through a Tuklas Lunas Center grant.