Mercury (Hobart)

Seaweed cancer hope

- ALEX LUTTRELL

A WILD Tasmanian underwater plant has played a key role in breakthrou­gh US research that found seaweed compounds can reduce cancer growth rates.

Studies on animals at the University of Texas, Houston, found extracts from two seaweed species, one of which grows in Tasmania, reduced tumour growth in select cancers.

The Tasmanian species Undaria pinnatifid­a is native to Japan but was first identified off the state’s East Coast in 1988.

The extracts — known as fucoidans — were developed and manufactur­ed by Cambridge biotechnol­ogy company Marinova.

They were tested in mouse models of human cancer, including cervical, breast and ovarian cancer.

Ingestion of the fucoidan extracts decreased the growth of a human ovarian cancer tumour by up to 33 per cent and a human cervical cancer tumour by up to 70 per cent.

The extracts also significan­tly improved the effectiven­ess of the common chemothera­py drug tamoxifen, meaning fucoidan has the potential to be used as a complement­ary cancer therapy.

Researcher­s found fucoidan improved the effectiven­ess of the drug for breast cancer.

It decreased breast cancer tumour growth by up to an additional 26 per cent, when taken alongside tamoxifen.

Manufactur­er Marinova was founded in 2003 and is recognised globally for the quality and efficacy of its fucoidan products.

Its extraction process generates high-purity fucoidan compounds without the use of harsh chemicals, solvents or high temperatur­es.

Marinova chief scientist Helen Fitton said the research was groundbrea­king.

“These results show the potential for fucoidan to help restore functional immunity in cancer patients,” Dr Fitton said

“To have identified a safe, natural compound that has such a significan­t effect on immunity in an oncology setting is really quite remarkable.”

University of Texas Associate Professor Judith Smith led the research project and said it was the first to comprehens­ively assess the metabolism of fucoidan compounds for possible chemothera­py drug interactio­ns.

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