Planta Med 2016; 82(S 01): S1-S381
DOI: 10.1055/s-0036-1596683
Abstracts
Georg Thieme Verlag KG Stuttgart · New York

A cytotoxic pentadecapeptide from a South African Didemnid tunicate

D Gallegos
1   Department of Pharmaceutical Sciences, College of Pharmacy, Oregon State University, Corvallis, OR 97331, USA
,
J Serrill
1   Department of Pharmaceutical Sciences, College of Pharmacy, Oregon State University, Corvallis, OR 97331, USA
,
S Parker-Nance
2   South African Institute of Aquatic Biosciences and Nelson Mandela Metropolitan University
,
R Dorrington
3   Rhodes University, Eastern Cape, South Africa
,
J Ishmael
1   Department of Pharmaceutical Sciences, College of Pharmacy, Oregon State University, Corvallis, OR 97331, USA
,
K McPhail
1   Department of Pharmaceutical Sciences, College of Pharmacy, Oregon State University, Corvallis, OR 97331, USA
› Author Affiliations
Further Information

Publication History

Publication Date:
14 December 2016 (online)

 
 

    The rate of discovery of new natural product chemical entities has plateaued, and unique populations of endemic, biologically diverse sessile marine organisms represent increasingly critical opportunities to discover new chemistry. Discovery of the mandelalides [1] as potent inhibitors of cancer cell growth from the new South African tunicate Lissoclinum mandelai is an example of the diverse suites of metabolites with potent biological activities that have been isolated from tunicates and other filter-feeding sessile marine organisms that house complex microbial consortia. Further investigation of archived and new tunicate collections from Algoa Bay, South Africa, has revealed a group of didemnid tunicates with an unusual gelatinous morphology similar to Lissoclinum mandelai. Using a bioassay-guided isolation approach, a new “gelatinous” species of the genus Didemnum has yielded a cytotoxic pentadecapeptide with a molecular mass of 1603.7688 Da, comprising fifteen residues including both proteinogenic and non-proteinogenic amino acids. The pure compound inhibited both HeLa cervical cancer and NCI-H460 non-small cell lung cancer cell lines when tested at 30 nM in preliminary assays against cells seeded at low densities. Inhibition of cancer cells at low starting density may be indicative of an anti-proliferative mechanism of action. The compound did not show antibacterial activity against Vibrio cholera. Didemnin B and its clinically approved analogue dehydrodidemnin B (plitidepsin, Aplidin®) [2, 3] are important macrocyclic depsipeptides from a didemnid tunicate. The pentadecapeptide reported here provides justification for our continued investigation of unique, endemic didemnid tunicates from South Africa as a source of new macrocyclic natural products with cytotoxic, anti-viral or antimicrobial activity.

    Acknowledgements: We acknowledge the South African government for permission to collect the subject tunicate (Collection Permit No. 278 RES2013/43).

    Keywords: Tunicates, natural products, cytotoxic, peptide, macrocycle, didemnid.

    References:

    [1] Sikorska J, Hau AM, Anklin, C, Parker-Nance S, Davies-Coleman MT, Ishmael JE, McPhail KL, Mandelalides AD. Cytotoxic macrolides from a new Lissoclinum species of South African tunicate. J Org Chem 2012; 77: 6066 – 6075

    [2] Shin DM, Holoye PY, Forman A, Winn R, Perez-Soler R, Dakhil S, Rosenthal J, Raber MN, Hong WK. Phase II clinical trial of didemnin B in previously treated small cell lung cancer. Invest New Drugs 1994; 12: 243 – 249

    [3] Urdiales J, Morata P, Castro IND, Sánchez-Jiménez F. Antiproliferative effect of dehydrodidemnin B (DDB), a depsipeptide isolated from Mediterranean tunicates. Cancer Lett 1996; 102: 31 – 37


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    No conflict of interest has been declared by the author(s).