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Review

Marine-Derived Steroids for Cancer Treatment: Search for Potential Selective Glucocorticoid Receptor Agonists/Modulators (SEGRAMs)

by
Ekaterina M. Zhidkova
1,
Ekaterina D. Savina
1,
Ekaterina A. Yurchenko
2 and
Ekaterina A. Lesovaya
1,3,4,*
1
Department of Chemical Carcinogenesis, Institute of Carcinogenesis, N.N. Blokhin National Medical Research Center for Oncology, Kashirskoe Shosse 24-15, Moscow 115478, Russia
2
G.B. Elyakov Pacific Institute of Bioorganic Chemistry, Far Eastern Branch of the Russian Academy of Sciences, 159 Prospect 100-Letiya Vladivostoka, Vladivostok 690022, Russia
3
Institute of Medicine, Peoples’ Friendship University of Russia, Miklukho-Maklaya St. 6, Moscow 117198, Russia
4
Faculty of Oncology, I.P. Pavlov Ryazan State Medical University, Vysokovol’tnaya Str 9, Ryazan 390026, Russia
*
Author to whom correspondence should be addressed.
Mar. Drugs 2025, 23(10), 399; https://doi.org/10.3390/md23100399 (registering DOI)
Submission received: 12 September 2025 / Revised: 11 October 2025 / Accepted: 13 October 2025 / Published: 14 October 2025
(This article belongs to the Special Issue Marine Natural Products as Anticancer Agents, 5th Edition)

Abstract

Steroids, particularly glucocorticoids, are essential components of cancer treatment for both hematological malignancies and solid tumors. The adverse effects of standard steroid-based drugs have forced drug discovery research to develop chemotherapeutics with a more selective mechanism of action and an improved therapeutic index. Steroids of natural origin and their analogs are a significant source of novel molecules with a wide spectrum of biological activities. In this review, we aimed to analyze marine-derived steroids and their anti-cancer activity. Moreover, we specifically discussed molecules with not only anti-cancer but also anti-inflammatory activities that could potentially mimic the effects of glucocorticoids. We hypothesized that several of the reviewed compounds could exhibit affinity to the glucocorticoid receptor, and possess the properties of selective glucocorticoid receptor agonists/modulators with increased therapeutic activity and decreased side effects. The review is based on the literature available in the PubMed, Cochrane, and ClinicalTrials.gov databases and covers the period from 1986 to 2025. The keywords used were “steroids”, “cancer”, and “marine-derived steroids”. The second iteration of the literature search included the keywords “selective glucocorticoid receptor agonists”, “marine-derived”, and “cancer”. In silico calculations of several marine-derived compounds were performed to support the hypothesis based on the literature data.
Keywords: marine-derived steroids; anti-cancer therapy; anti-inflammatory effects; glucocorticoid; selective glucocorticoid receptor agonists marine-derived steroids; anti-cancer therapy; anti-inflammatory effects; glucocorticoid; selective glucocorticoid receptor agonists

Share and Cite

MDPI and ACS Style

Zhidkova, E.M.; Savina, E.D.; Yurchenko, E.A.; Lesovaya, E.A. Marine-Derived Steroids for Cancer Treatment: Search for Potential Selective Glucocorticoid Receptor Agonists/Modulators (SEGRAMs). Mar. Drugs 2025, 23, 399. https://doi.org/10.3390/md23100399

AMA Style

Zhidkova EM, Savina ED, Yurchenko EA, Lesovaya EA. Marine-Derived Steroids for Cancer Treatment: Search for Potential Selective Glucocorticoid Receptor Agonists/Modulators (SEGRAMs). Marine Drugs. 2025; 23(10):399. https://doi.org/10.3390/md23100399

Chicago/Turabian Style

Zhidkova, Ekaterina M., Ekaterina D. Savina, Ekaterina A. Yurchenko, and Ekaterina A. Lesovaya. 2025. "Marine-Derived Steroids for Cancer Treatment: Search for Potential Selective Glucocorticoid Receptor Agonists/Modulators (SEGRAMs)" Marine Drugs 23, no. 10: 399. https://doi.org/10.3390/md23100399

APA Style

Zhidkova, E. M., Savina, E. D., Yurchenko, E. A., & Lesovaya, E. A. (2025). Marine-Derived Steroids for Cancer Treatment: Search for Potential Selective Glucocorticoid Receptor Agonists/Modulators (SEGRAMs). Marine Drugs, 23(10), 399. https://doi.org/10.3390/md23100399

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