Genome packaging: Key to breast cancer development

November 22, 2012
Genome packaging: Key to breast cancer development
Dividing breast cancer cell stained for DNA, Tubulin and Progesterone receptor.

Cancer is a complex disease and only thanks to advances in genomic techniques have researchers begun to understand, at a cellular and molecular level, the mechanisms which are disrupted in cancer cells. This knowledge is a key prerequisite for developing effective treatment strategies.

One clear example of this is breast cancer. It has long been known that hormones such as and progesterone encourage the proliferation of . Because of this, one of the most common treatments is the administration of blockers. The block, however, affects all the cells of the body not only the cancer cells, and causes a number of side effects in patients. Additionally, most cancers develop resistance after time and growth continues despite anti-hormone therapy. In order to treat these patients it is necessary to understand the mechanisms that trigger proliferation, in order to inhibit them.

The scientists from the Chromatin and Gene Expression lab at the CRG, led by Miguel Beato, are dedicated to understanding how hormones activate cell division in breast cancer, focusing on regulating the expression of the genes that control the cell cycle.

Hormone receptors are transcription factors that bind to DNA sequences in the vicinity of the genes they regulate. But the DNA of the genes is packed into a dense structure known as "chromatin", which is considered a barrier preventing the access of transcription factors to genes. Therefore the chromatin must be decompacted for the to activate the , express RNA and subsequently translate them into proteins that stimulate . This is where progesterone, via its receptor, activates various enzymes initiating chromatin opening.

In the study published on September 1 in the journal Genes & Development, the researchers looked at the role of an enzyme, PARP-1, which is primarily responsible for the repair of cuts in DNA. "We have found a novel mechanism of PARP-1 activation, via another enzyme, CDK2, which phosphorylates and activates PARP-1, essential for chromatin opening and gene regulation.", explains Roni Wright, first author of the study. Wright is a postdoctoral researcher in Beato's lab. She believes that much remains to be discovered in this area of research. "This experiment was conducted on cell lines, but now we have to do it on real, patient cells to see if their behaviour is the same", adds the researcher.

How do we know how the proliferation of cancer cells is controlled?

Gene regulation (how genes activate and deactivate) is the key to the overall understanding of how our genome works and how it is altered in disease. "It is important to discover the mechanism by which genes are activated around chromatin", explains Miguel Beato. The chromatin packs the DNA at several levels, the first being the "nucleosomes", which help stabilise the DNA chain. "It was thought that the chromatin structure was not relevant to explaining how genes turn on and off, but we have discovered that it is crucial," adds Beato.

The second study, published online on November 21, 2012 in the journal Molecular Cell, addresses this issue. Firstly, all the genes that progesterone activates or represses in cells were identified. Then the researchers identified which recognise the progesterone receptor in the genome. They found that these represented only a small proportion of the possibilities, making them think that interaction with DNA was not sufficient. It was necessary for the sequences which bind to the receptor to be incorporated into nucleosomes, which also provide interaction sites.

"It appears that the structure of is fundamental for determining the activation or repression of genes."says Cecilia Ballaré, first author of the paper.

The researchers believe that the only way to create increasingly specific and effective cancer treatments is by studying the role of all the elements that regulate and cell proliferation in response to hormones. "Knowing the exact way progesterone affects the proliferation of cancer cells may help develop more specific treatments that fight only cancer cells and thus produces fewer side effects", adds Ballaré.

Explore further: Team genetically sequences most common bladder cancer

More information: Wright, R. H. et al. "CDK2-dependent activation of PARP-1 is required for hormonal gene regulation in breast cancer cells". Genes & Dev. (2012). 26: 1972-1983. doi: 10.1101/gad.193193.112

Ballare ́, C. et al. "Nucleosome-Driven Transcription Factor Binding and Gene Regulation". Molecular Cell (11 Enero, 2013),

Wright R, Beato M. PARty promoters: Hormone-dependent gene regulation requires CDK2 activation of PARP1. Cell Cycle 2012; 11:0 - 2; PMID: 23095674.

Related Stories

Team genetically sequences most common bladder cancer

August 11, 2011

In an article published online this week in Nature Genetics, a University of Colorado Cancer Center team in partnership with universities in China and Denmark reports the first genetic sequencing of urothelial (transitional) ...

Recommended for you

Ancient stress response provides clues to cancer resistance

April 25, 2017

Cancer is often able to craftily outwit the best techniques modern medicine has developed to treat it. In an attempt to understand and combat cancer's vaunted prowess, an unusual collaboration between physicists and a leading ...

Studying a catalyst for blood cancers

April 25, 2017

Imagine this scenario on a highway: A driver starts to make a sudden lane change but realizes his mistake and quickly veers back, too late. Other motorists have already reacted and, in some cases, collide. Meanwhile, the ...


Please sign in to add a comment. Registration is free, and takes less than a minute. Read more

Click here to reset your password.
Sign in to get notified via email when new comments are made.