My father died of non-Hodgkins lymphoma
at 49. Although the initial prognosis was
positive, treatments of the day, 15 years ago, were unsuccessful. Unfortunately, tumours in his bowel grew
while he was being treated, and it got to the point where there were no more
options. Cancer treatment has often been
a balance between killing the tumour without quite killing the person. So it’s with a very real human understanding
that I, and many of us approach the ideas about cancer and treatment therapies,
and the possibilities of targeting defective tissue and protecting healthy
tissue.
Cancer is a disease that seems to
attract a lot of very emotive language that almost personifies cancer. We talk about ‘fighting’ cancer. We think about it in sinister terms and use
words such as rampant, ravage, riddled.
Cancer is special in this way – we don’t really ‘battle’ heart disease. For many without a decent understanding of
biology and molecules (ie me), the idea of mutating viruses and enzymes for
cancer treatment is up there with human cloning, or nano-robots as some sort of
science fiction premise for a great movie. Enter Spiderman’s psychotic professor. Fortunately,
Dave Ackerly is no such character. He is
easy to listen to and understand, thoughtful and empathetic, and most of all
uber excited about his field of scientific research. It’s so much easier to learn from people who
are excited about their work. So this
course has been better than therapy for me. I have had a mechanism to think
about my father and his ‘battle’ with cancer in a productive, hopeful way.
(All biological understanding is from D. Ackerley, Scie211, Module 2, Lectures 1-4, Genes & Gene Therapy 2013/2014)
Understanding the biological basis of
cancerous ‘events’ as Dave Ackerley, gene therapy researcher at Victoria University refers to them, the more we can
target defective cells that grow into tumours.
These cells don’t behave as healthy cells do; they over-replicate, they
grow, they create tumours that prevent the body from functioning as it is
supposed to such as tumours that restrict the bowel. But the more we know about tumours the more we
can use their characteristics to develop potential treatment methods. Tumours function in hypoxic environments,
and there are viruses and bacteria that also thrive in hypoxic environments
such as clostridium. These invaders can
be developed (mutated) in the lab by methods of directed evolution to function
in useful ways, by carrying and releasing enzymes in hypoxic conditions that
then sensitise the tumour to further treatments. Developments of these directed space invaders are alongside the development of better prodrugs that are designed to be non-toxic to human tissue but become toxic
when in contact with certain enzymes – enter Ackerleys mutated nitro
reductase. Well that’s the plan
anyway. It’s a few years away from
helping patients such as my father, but I know for sure he would have jumped at
the chance to participate in clinical trials – not only for his own potential
benefit but others.
(All biological understanding is from D. Ackerley, Scie211, Module 2, Lectures 1-4, Genes & Gene Therapy 2013/2014)
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