University
of Otago scientists studying a previously unexploited
weakness in HIV biology are taking "an exciting new step" by
seeking drugs to attack it.
Prof Warren Tate, a leading international biochemistry
researcher, is the principal investigator in an HIV research
programme which has just gained a Health Research Council
grant of $396,538 to advance the drug search efforts.
Prof Richard Cannon, of the Otago University oral sciences
department, has also received a grant of $333,622 to pursue
melanoma-related research.
Prof Tate, of Otago University, said the grant for HIV
research would enable the team to take its research "to the
next stage".
Much more work still had to be done, but the weak point in
HIV biology - involving its regulation of the synthesis of
structural and enzyme proteins - was a promising target.
"We've got to remain optimistic."
The grant, spread over two years, is the largest of three
recently made by the ARC throughout New Zealand, and
totalling $1.1 million.
The overall funding is aimed at helping build international
health research partnerships.
Prof Tate said it was "absolutely essential" new anti-HIV
drugs be developed. This was partly because of potential
problems with drug resistance and toxic side effects among
the cocktail of existing drugs used to treat HIV.
The nature of the genetic target, which had long been studied
by Otago researchers, meant that drugs to exploit it were
likely to be less subject to HIV adaptation and resistance.
"That could be a big plus."
Dr Tony Cardno, a postdoctoral researcher in Prof Tate's
research group, has developed a new cell-based test, which
has been patented, to explore the novel target in HIV-1, the
most common form of HIV.
Aids is caused by HIV.
HIV-1 used a rare and "highly unusual" genetic mechanism to
regulate synthesis of its structural and enzyme proteins in
the correct amounts crucial for infectivity. If the mechanism
could be disrupted, HIV infectiousness could also be greatly
reduced.
The research funding gained by Prof Cannon involves melanoma,
the most dangerous form of skin cancer.
The cancer caused 249 deaths in New Zealand in 2004.
Surgery could be used to treat early stage melanoma, but the
cancer was lethal in advanced stages, researchers said.
Chemotherapy was not usually employed, as melanomas were
highly resistant to many anti-cancer drugs, and the melanoma
progenitor cells expressed the drug efflux pump Abacas.
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