Calculating how breast cancers will respond to tamoxifen
A discovery by Australian scientists could help clinicians decide
which women with breast cancer will make good candidates for
anti-oestrogen therapies, such as tamoxifen, and which will not.
Over 12,000 Australian women are diagnosed with breast cancer each
year, roughly 70% of which will have cancers treatable with tamoxifen.
Unfortunately, 30% or more of these women may not respond well to such
anti-hormone therapy long-term.
Work done by a research team headed by Associate Professor Liz Musgrove
and Professor Rob Sutherland of Sydney’s Garvan Institute of Medical
Research has correlated expression of certain functionally-related
oestrogen-regulated genes with predictable clinical outcomes. This
expanded knowledge about oestrogen action and endocrine resistance
should allow clinicians to make better, more informed, choices in the
future.
The novel findings were published in the August issue of the Public
Library of Science journal PLoS ONE.
“What we call ‘breast cancer’ is actually many different kinds of
cancer, some of which appear to be driven by the female hormone
oestrogen,” said Professor Musgrove. “We found roughly 800 genes that
are regulated by oestrogen, each with a different function in the cell,
so you can imagine how complicated the picture can become when you are
trying to correlate the effects of all these genes with multiple
cancers.”
In fact, the scale of such calculations, and complex biochemistry
behind them, requires the help of large relational databases, powerful
software and the agile minds of bioinformatics specialists to crunch
and analyse data.
Out of the undifferentiated pool of oestrogen-regulated genes, the team
has identified four groupings of genes, with each group relating to one
aspect of breast cancer cell behaviour: cell cycle (proliferation),
cell growth (actual size of the cell), cell death and gene
transcription.
Professor Musgrove stresses the clinical relevance of the findings. “In
collaboration with colleagues at the Peter MacCallum Cancer Centre in
Melbourne, we took these 4 groups of genes and asked whether they were
related to outcome in a sample of 246 women who’d been treated with
tamoxifen. We were able to directly relate 3 out of the 4 groups, all
but gene transcription, to whether a woman had done better or worse
when treated with tamoxifen.”
“We then went on to ask whether we were looking at three different ways
of identifying the same women, or whether the three groups of genes
identified distinct groups of women, with different breast cancers. It
appears as if they identify distinct groups of women with different
cancers.”
“Developing pure lists of genes that are involved in single processes
gives us a good conceptual and experimental framework. In time we hope
to understand how these groups of genes interact, and exactly how they
affect disease or health.”
ABOUT GARVAN
The Garvan Institute of Medical Research was founded in 1963.
Initially a research department of St Vincent's Hospital in Sydney, it
is now one of Australia's largest medical research institutions with
approximately 400 scientists, students and support staff. Garvan's main
research programs are: Cancer, Diabetes & Obesity, Immunology and
Inflammation, Bone, and Neuroscience. The Garvan's mission is to make
significant contributions to medical science that will change the
directions of science and medicine and have major impacts on human
health. The outcome of Garvan's discoveries is the development of
better methods of diagnosis, treatment, and ultimately, prevention of
disease.
All media enquiries should be directed to:
Alison Heather 0434 071 326 or Jackie Crossman on 0402 218 662



