Australian researchers have found there are two different types of ‘triple-negative breast cancers’ – the most dangerous of breast cancer types – based on the types of cells they originate from. Researchers have found a gene that drives the aggressive disease and hope to find a way to ‘switch it off’.
Researchers have found that the more aggressive form of triple-negative breast cancer appears to arise from stem cells, while the more benign form appears to arise from specialised cells.
Previous studies have shown that breast stem cells are needed for breast growth and development during puberty and pregnancy, although how they evolve from stem cells into specialist cells has been unclear.
The latest study shows that a gene known as ‘inhibitor of differentiation 4’ (ID4) determines whether a stem cell remains a stem cell, or whether it differentiates into a specialist cell. Notably, when the high levels of ID4 in a stem cell are ‘switched off’, other genes that drive cell specialisation are ‘switched on’.
Dr Alex Swarbrick and Dr Simon Junankar from Sydney’s Garvan Institute of Medical Research spearheaded this large interdisciplinary study, which links the development of the mammary gland in mice with human breast cancer. Its main finding, that ID4 not only ‘marks’, but appears to control, the highly aggressive form of triple negative breast cancer is published online today in Nature Communications.
“We found that ID4 is produced at high levels in roughly half of all triple negative breast cancers, and that these cancers have a particularly poor prognosis,” said project leader Dr Alex Swarbrick.
“We also showed that if you block the ID4 gene in experimental models of triple negative breast cancer, the tumour cells stop dividing.”
It is interesting to note that blocking ID4 switches on the oestrogen receptor3 and several other genes expressed by the best-prognosis breast cancer.
“Oestrogen receptor-positive breast cancers have a relatively good prognosis because the drug Tamoxifen is very effective at blocking the oestrogen receptor and hence their growth” noted Swarbrick.
“We speculate, therefore, that by blocking ID4 it might be possible to turn stem-cell-like breast cancers into less aggressive breast cancers that may even respond to tamoxifen. If we are correct, that would be remarkable.”
The next step for Dr Swarbrick and his team will be to study the biochemistry of ID4 in a cell – to determine how best to block it in people.
There are also plans to undertake therapeutic experiments in mice to test whether or not switching off ID4 sensitises a tumour to tamoxifen.
“We don’t know yet whether we are seeing a real oestrogen-dependent cancer after ID4 is blocked – one with an effective oestrogen receptor – or just a caricature of one.
“We’re very fortunate that our collaborator in Cambridge UK is a world expert on oestrogen receptor function.
“We also have technologies that allow us to study processes on a genome-wide scale – so we can map the interactions of ID4 comprehensively.”
