Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2014 Jan 14;12(1):255-78.
doi: 10.3390/md12010255.

Marine-sourced anti-cancer and cancer pain control agents in clinical and late preclinical development

Affiliations
Review

Marine-sourced anti-cancer and cancer pain control agents in clinical and late preclinical development

David J Newman et al. Mar Drugs. .

Abstract

The marine habitat has produced a significant number of very potent marine-derived agents that have the potential to inhibit the growth of human tumor cells in vitro and, in a number of cases, in both in vivo murine models and in humans. Although many agents have entered clinical trials in cancer, to date, only Cytarabine, Yondelis® (ET743), Eribulin (a synthetic derivative based on the structure of halichondrin B), and the dolastatin 10 derivative, monomethylauristatin E (MMAE or vedotin) as a warhead, have been approved for use in humans (Adcetris®). In this review, we show the compounds derived from marine sources that are currently in clinical trials against cancer. We have included brief discussions of the approved agents, where they are in trials to extend their initial approved activity (a common practice once an agent is approved), and have also included an extensive discussion of the use of auristatin derivatives as warheads, plus an area that has rarely been covered, the use of marine-derived agents to ameliorate the pain from cancers in humans, and to act as an adjuvant in immunological therapies.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Pain control agents
Figure 2
Figure 2
Approved marine-derived drugs and close analogues in clinical trials.
Figure 3
Figure 3
Other marine-derived compounds in phase I–III trials.

References

    1. Turabi A., Plunkett A.R. The application of genomic and molecular data in the treatment of chronic cancer pain. J. Surg. Oncol. 2012;105:494–501. doi: 10.1002/jso.21707. - DOI - PubMed
    1. Nieto F.R., Cobos E.J., Tejada M.Á., Sánchez-Fernández C., González-Cano R., Cendán C.M. Tetrodotoxin (TTX) as a therapeutic agent for pain. Mar. Drugs. 2012;10:281–305. doi: 10.3390/md10020281. - DOI - PMC - PubMed
    1. Moczydlowski E.G. The molecular mystique of tetrodotoxin. Toxicon. 2013;63:165–183. doi: 10.1016/j.toxicon.2012.11.026. - DOI - PubMed
    1. Chau R., Kalaitzis J.A., Neilan B.A. On the origins and biosynthesis of tetrodotoxin. Aquat. Toxicol. 2011;104:61–72. doi: 10.1016/j.aquatox.2011.04.001. - DOI - PubMed
    1. Nishikawa T., Isobe M. Synthesis of tetrodotoxin, a classic but still fascinating natural product. Chem. Rec. 2013;13:286–302. doi: 10.1002/tcr.201200025. - DOI - PubMed

LinkOut - more resources