AI Article Synopsis

  • Cancer is the second leading cause of death globally, and there's an urgent need for new cancer therapies, prompting research into natural and synthetic chemotherapeutic drugs.
  • Mangrove-derived fungi present a rich source of novel metabolites, which may have unique mechanisms and structures suitable for developing new anticancer drugs.
  • The review discusses bioactive compounds from mangrove endophytes identified between 2012 and 2018, highlighting their cytotoxic properties and potential as lead molecules in cancer treatment.

Article Abstract

Cancer is the second leading cause of death worldwide, and the number of cases is increasing alarmingly every year. Current research focuses on the development of novel chemotherapeutic drugs derived from natural as well as synthetic sources. The abundance and diversity in natural resources offer tremendous potential for the discovery of novel molecules with unique mechanisms for cancer therapy. Mangrove-derived fungi are rich source of novel metabolites, comprising novel structure classes with diverse biological activities. Across the globe, coastal areas are primarily dominated by mangrove forests, which offer an intensely complex environment and species that mostly remain unexplored. In recent years, many structurally diverse compounds with unique skeletons have been identified from mangrove fungi and evaluated for their antiproliferative properties. These compounds may serve as lead molecules for the development of new anticancer drugs. Mangrove endophytes can be modulated using epigenetic means or culture optimization methods to improve the yield or to produce various similar analogs. The present review provides an insight into the bioactive metabolites from mangrove endophytes reported during the period from 2012 to 2018 (up to April, 2018) along with their cytotoxic properties, focusing on their chemical structures and mode of action, as indicated in the literature.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6162443PMC
http://dx.doi.org/10.3390/jof4030101DOI Listing

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