Related Experiment Video
Updated: May 13, 2026

A Tripeptide-Stabilized Nanoemulsion of Oleic Acid
Published on: February 27, 2019
Isolation, Structures, and Mechanisms of Anti-Tumor Peptides from Marine Organisms: A Review
Xueer Xu1,2, Jiahua Peng1,3, Hui Shi1,3
1Dongguan Key Laboratory of Traditional Chinese Medicines for Prevention and Treatment of Digestive Diseases, Guangdong Medical University, Dongguan, Guangdong, 523808, China.
Abstract:
Anti-tumor drugs research has long been a key area of drug discovery because cancer remains one of the deadliest diseases globally, with over 10 million deaths annually and increasing resistance to conventional therapies. Therefore, there is an urgent need to explore novel therapeutic approaches and develop new anti-tumor agents with low toxicity. With over 25,000 fish species and one million marine invertebrates, the oceans represent an under-explored reservoir of bioactive compounds, where marine anti-tumor peptides exhibit unique advantages including low intrinsic toxicity, high tissue penetration, and specificity towards cancer cells that address critical limitations of chemotherapeutic drugs, such as off-target effects and multidrug resistance. However, the field currently lacks a comprehensive and systematic analyses that integrate recent advances in discovery, mechanistic elucidation, and translational challenges. This review covers key aspects such as isolation techniques, purification processes, structural characterization techniques, and diverse antitumor mechanisms. Its goal is to summarize and analyze the current state, trends, and research advancements of anti-tumor peptides isolated and extracted from marine organisms. Additionally, this review systematically compiles peptide structures with clinical potential and dissects the key obstacles in their drug development pathways. By integrating this knowledge, the review not only serves as a valuable reference for researchers but also offers critical insights into the strategic roadmap for harnessing marine peptides in the fight against cancer.
Insights
Marine anti-tumor peptides offer a promising avenue for cancer therapy due to their low toxicity and high specificity. This review explores their discovery, mechanisms, and challenges for developing novel anti-cancer drugs.
Area of Science:
- Marine biotechnology
- Drug discovery
- Cancer research
Background:
- Cancer is a leading global cause of death, with increasing resistance to conventional therapies.
- Marine organisms are a rich source of novel bioactive compounds.
- Marine anti-tumor peptides present unique advantages over traditional chemotherapeutics.
Purpose of the Study:
- To systematically review the current state and advancements in marine anti-tumor peptides.
- To analyze discovery, mechanistic elucidation, and translational challenges.
- To compile peptides with clinical potential and identify drug development obstacles.
Main Methods:
- Literature review and synthesis of existing research on marine anti-tumor peptides.
- Analysis of isolation, purification, and structural characterization techniques.
- Examination of antitumor mechanisms and clinical potential.
Main Results:
- Marine peptides exhibit low toxicity, high tissue penetration, and cancer cell specificity.
- Diverse antitumor mechanisms are employed by these peptides.
- Key challenges in marine peptide drug development pathways were identified.
Conclusions:
- Marine anti-tumor peptides represent a significant, under-explored resource for novel cancer therapeutics.
- Further research and strategic development are crucial to overcome translational challenges.
- This review provides a roadmap for harnessing marine peptides in oncology.
Related Concept Videos
Drugs that Stabilize Microtubules
Targeted Cancer Therapies
There are several types of targeted therapies against specific...
Metastasis
Epithelial-to-Mesenchymal Transition
The epithelial-to-mesenchymal transition or EMT is a developmental process commonly observed in wound healing, embryogenesis, and cancer metastasis. EMT is induced by transforming growth factor-beta (TGF-β) or receptor tyrosine kinase (RTK) ligands, which further...