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

Mar Drugs

Natural Products Branch, Developmental Therapeutics Program, Division of Cancer Treatment and Diagnosis, Frederick National Laboratory, P.O. Box B, Frederick, MD 21702, USA.

Published: January 2014

AI Article Synopsis

  • The marine environment has yielded various potent compounds that show promise in fighting cancer, both in lab settings and in clinical patients.
  • So far, only a few marine-derived agents like Cytarabine and Yondelis® have gained approval for human use, while others remain in ongoing clinical trials.
  • The review highlights these compounds, covering their approved uses, current trials for enhanced effectiveness, and the potential of marine agents in pain management and immunotherapy support.

Article 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3917273PMC
http://dx.doi.org/10.3390/md12010255DOI Listing

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