A bacterial strain that specifically targets tumours could soon be
used as a vehicle to deliver drugs in frontline cancer therapy. The strain is
expected to be tested in cancer patients in 2013, says a scientist at the
Society for General Microbiology's Autumn Conference at the University of York.
The therapy uses Clostridium sporogenes -- a
bacterium that is widespread in the soil. Spores of the bacterium are injected
into patients and only grow in solid tumours, where a specific bacterial enzyme
is produced. An anti-cancer drug is injected separately into the patient in an
inactive 'pro-drug' form. When the pro-drug reaches the site of the tumour, the
bacterial enzyme activates the drug, allowing it to destroy only the cells in
its vicinity -- the tumour cells.
Researchers at the University of Nottingham and the University of
Maastricht have now overcome the hurdles that have so far prevented this
therapy from entering clinical trials. They have introduced a gene for a
much-improved version of the enzyme into the C. sporogenes DNA. The improved
enzyme can now be produced in far greater quantities in the tumour than
previous versions, and is more efficient at converting the pro-drug into its
active form.
A fundamental requirement for any new cancer therapy is the
ability to target cancer cells while excluding healthy cells. Professor Nigel
Minton, who is leading the research, explains how this therapy naturally
fulfils this need. "Clostridia are an ancient group of bacteria that
evolved on the planet before it had an oxygen-rich atmosphere and so they
thrive in low oxygen conditions. When Clostridia spores are injected into a
cancer patient, they will only grow in oxygen-depleted environments, i.e. the
centre of solid tumours. This is a totally natural phenomenon, which requires
no fundamental alterations and is exquisitely specific. We can exploit this
specificity to kill tumour cells but leave healthy tissue unscathed," he
said.
The research may ultimately lead to a simple and safe procedure
for curing a wide range of solid tumours. "This therapy will kill all
types of tumour cell. The treatment is superior to a surgical procedure,
especially for patients at high risk or with difficult tumour locations,"
explained Professor Minton. "We anticipate that the strain we have
developed will be used in a clinical trial in 2013 led by Jan Theys and
Philippe Lambin at the University of Maastricht in The Netherlands. A
successful outcome could lead to its adoption as a frontline therapy for
treating solid tumours. If the approach is successfully combined with more
traditional approaches this could increase our chance of winning the battle
against cancerous tumours."
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