Abstract

Oncological diseases for a long time have remained one of the most significant health problems of modern society, which causes great losses in its labour and vital potential. Contemporary oncology still faces unsolved issues as insufficient efficacy of treatment of progressing and metastatic cancer, chemoresistance, and side-effects of the traditional therapy which lead to disabilities among or death of a high number of patients. Development of new anti-tumour preparations with a broad range of pharmaceutical properties and low toxicity is becoming increasingly relevant every year. The objective of the study was to provide a review of the recent data about anti-tumour preparations of marine origin currently being at various phases of clinical trials in order to present the biological value of marine organisms – producers of cytotoxic compounds, and the perspectives of their use in modern biomedical technologies. Unlike the synthetic oncological preparations, natural compounds are safer, have broader range of cytotoxic activity, can inhibit the processes of tumour development and metastasis, and at the same time have effects on several etiopathogenic links of carcinogenesis. Currently, practical oncology uses 12 anti-tumour preparations of marine origin (Fludarabine, Cytarabine, Midostaurin, Nelarabine, Eribulin mesylate, Brentuximab vedotin, Trabectedin, Plitidepsin, Enfortumab vedotin, Polatuzumab vedotin, Belantamab mafodotin, Lurbinectedin), 27 substances are at different stages of clinical trials. Contemporary approaches to the treatment of oncological diseases are based on targeted methods such as immune and genetic therapies, antibody-drug conjugates, nanoparticles of biopolymers, and metals. All those methods employ bioactive compounds of marine origin. Numerous literature data from recent years indicate heightened attention to the marine pharmacology and the high potential of marine organisms for the biomedicinal and pharmaceutic industries.

Highlights

  • Malignant tumors create a significant social problem and have for many years continuned to be the main constituent of non-infectious diseases, causing significant losses of labour and vital potential of society

  • According to the predictions of the experts of the World Health Organization (WHO) and the International Agency for Research on Cancer (IARC), in the period of 2012 to 2030, the global number of cases of cancer found for the first time will increase from 14 M to almost 22 M people, and will grow to 27.5 by 2040 (American Cancer Society (ACS) Global Cancer Facts & Figures

  • Cyanobacteria / Multiple solid tumours, The first and the only agent aimed at nectin-4, Newman, 2019; 22MSE) / Agensys, Seattle metastatic cancers of the molecule of cellular adhesion, which expresses on Pereira, 2019; Genetics, Astellas Pharma urinary system and the many solid tumours

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Summary

Regulatory Mechanisms in Biosystems

Anti-tumour drugs of marine origin currently at various stages of clinical trials (review). The objective of the study was to provide a review of the recent data about anti-tumour preparations of marine origin currently being at various phases of clinical trials in order to present the biological value of marine organisms – producers of cytotoxic compounds, and the perspectives of their use in modern biomedical technologies. Contemporary approaches to the treatment of oncological diseases are based on targeted methods such as immune and genetic therapies, antibody-drug conjugates, nanoparticles of biopolymers, and metals. All those methods employ bioactive compounds of marine origin.

Introduction
Marine organisms producing cytotoxic compounds
Mechanism of action
Volwassenen Nederland
Hodgkin lymphoma
Phase III
Depatuxizumab mafodotin
Phase II
Telisotuzumab vedotin
Inductor of stable proliferation and production of interleukins of iNKT cells
Cirmtuzumab vedotin
Ladiratuzumab vedotin
Enapotamab vedotin
Phase I
Keyhole Limpet
Phase of study
Orphan drug in combination with stimulator
Aims at epithelial prostate antigene
Seattle Genetics
Trials of biopharmaceutic production
Findings
Conclusions
Full Text
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