Media Release: 27 September 2010
Australian and American scientists have found a way of shrinking tumours in certain cancers – a finding that provides hope for new treatments.
The cancers in question are those caused by a new class of genes known as ‘microRNAs’, produced by parts of the genome that, until recently, were dismissed as ‘junk DNA’. While much is still unknown about microRNAs, it is clear that they can interfere with how our genes are ‘read’.
The current finding identifies one particular microRNA (microRNA 380) that appears to disable the king of tumour suppressors, the P53 gene. So important is P53, that it is known as the ‘guardian of the genome’. In order for a cell to become cancerous, P53 must either be mutated or otherwise disabled.
Dr Alex Swarbrick, from Sydney’s Garvan Institute of Medical Research, Dr Susan Woods from Brisbane’s Queensland Institute of Medical Research and Dr Andrei Goga from The University of California San Francisco chose to study neuroblastoma, a childhood cancer of the nervous system in which 99% of patients do not have mutations of the P53 gene.
The researchers found instead that neuroblastomas disable p53 by over-producing microRNA 380. When they blocked the microRNA, P53 production resumed, cancer cells died and tumours became much smaller. Their results are reported in the prestigious international journal Nature Medicine, online today.
“The revolutionary thing about this finding is that it’s the first time anyone has blocked the growth of a primary tumour by the simple delivery of a microRNA inhibitor,” said Swarbrick.
“By that, I mean we delivered the microRNA inhibitor in a way we might give it to a person – as a twice-weekly injection – not using some genetic trick. It’s the closest thing to a clinical result that’s yet been published.”
“That, of course, makes this microRNA a potential therapeutic target for all cancers that depend on it.”
“The other good news is that you don’t find this microRNA in normal adult cells. It’s very active while we are developing embryos, when cells need to divide very quickly, but after that it appears to get switched off. So by blocking it, you’re effectively returning cells to normal.”
“We still don’t know why it gets switched on again in certain cancers. Apart from neuroblastomas, we often see it in brain tumours and in melanomas that don’t have mutations in P53.”
So how exactly does it work?
When a gene is transcribed or “read”, in this case P53, a copy of the gene is made in RNA. In a normal cell, that P53 RNA carries the instructions to make P53 proteins, which in turn carry out the tumour suppressor function in cells.
“MicroRNAs act to control the production of proteins – the molecules that do the work in cells,” explained Swarbrick.
“In the cancers we are discussing, our microRNA binds with P53 RNA, preventing it from making proteins. That effectively reduces the number of P53 proteins in a cell and allows the tumour to grow.”
“Understanding that certain cancers appear to be regulated like this gives us a new avenue to explore in their treatment.”
While this finding is at an early research stage, it holds much promise for the future treatment of early childhood neuroblastomas and other microRNA- induced cancers.
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We would like to thank J. M. Bishop, N. K. Hayward and R. L. Sutherland for their support of this project, the Children's Oncology Group and Matt M. Grimmer for providing tumor samples, D. Lynch and J. Brugge for MCF10A cells expressing the ecotropic receptor, R. Jaenisch for Ttp53-/- ES cells and S. Lowe for the p53 shRNA retrovirus.
This work was supported by grants from the US National Institutes of Health P50-CA58207, K08-CA104032, 1R01CA136717, 5R01DC005991 (to N.L.), R01CA102321, R01NS055750, P01CA081403 (to W.W.), K08NS48118 (to R.B.); the S.G. Komen Foundation; the UCSF Program for Breakthrough Biomedical Research (to A.G.); the G.W. Hooper Foundation; the Australian National Health and Medical Research Council (to T.P, M.H., M.N. and A. Swarbrick) and the Cancer Institute NSW (M.H. and M.N.).
A. Swarbrick is a recipient of a Cancer Institute NSW early career development fellowship and R.L.J a US National Science Foundation fellowship. A.G. is a V-Foundation Scholar, A. Shaw is a Cancer Institute NSW Research Scholar and Y.P. is supported by an Australian Postgraduate Award from the Australian National Health and Medical Research Council.