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How Breast Cancer Cells Evade Therapeutic Attacks

May 10, 2010
by Vicki Tashman, Founder of Pink-Link

Tumor cells depend upon estrogens to survive and proliferate in about 70% of all breast cancer cases. The most frequently used treatment to fight this variety of tumors relies on anti-estrogens such as tamoxifen. However, resistance to this type of therapy develops in more than 30% of the patients. Understanding the mechanisms involved in the appearance of resistance to tamoxifen is thus essential to develop new therapeutic approaches.

 

The research, done by the team of Didier Picard, professor at the University of Geneva (UNIGE), provides key answers in the journal Genes & Development. Their study reveals how cancer cells become impervious to the drug by activating a specific biochemical cascade. The latter, normally triggered by a chemical messenger called cyclic AMP, is permanently stimulated in cells refractory to the treatment.

 

Breast cancer, which is characterized by an enhanced and anarchic proliferation of mammary cells, is one of the main causes of cancer-related mortality in women. In over two thirds of the cases, estrogens play an active part in the progression of the disease, due to the presence of receptors for this hormone in the nucleus of malignant cells. Estrogens indeed modulate the expression of genes necessary to cell survival and proliferation through their interaction with these receptors.

 

The most frequent treatment for this type of breast cancer, called hormone-dependent, relies on anti-estrogens such as tamoxifen, which block tumor cell growth by inhibiting the activity of the receptor. However, the cancer eventually becomes resistant to the therapy in more than 30% of the patients.

 

"Estrogen receptors, notably the one called ERα, are also activated by other molecules that operate in an indirect way, without interacting with them", explains Didier Picard, professor at the Faculty of Sciences of UNIGE. "We aim precisely at understanding the mechanisms involved in the indirect stimulation of ERα in cancer cells."

 

Researchers from his team have studied a molecule, cyclic AMP, which is able to convey various types of signals within the cell. Called a "second messenger," this molecule acts as an intermediary to transmit information between the exterior and the interior of the cell. Different growth factors, neurotransmitters or hormones, incapable of crossing the cell barrier, thus communicate their message by activating intracellular signaling pathways via cyclic AMP.

 

"During this project, we have studied how cyclic AMP could turn on ERα in breast cancer cells in the absence of estrogens," says lead author Sophie Carascossa. In this case, the second messenger triggers a specific biochemical signaling cascade in which a protein called CARM1 is involved. The protein then binds ERα and this in turn activates the receptor. "The interaction with CARM1 occurs in a domain of the receptor near the one that normally binds estrogens. This mode of regulation was completely unknown until now," specifies the scientist. The study also reveals that the signaling pathway is stimulated in a constitutive way in malignant cells resistant to tamoxifen, thus evading control in these cells.

 

Although the molecular mechanisms implicated in the resistance process are probably numerous, the interaction between CARM1 and ERα could represent a promising therapeutic target in the long run.

 

SOURCES:

 

Genes & Development, April 1, 2010

University of Geneva (http://www.unige.ch)

Cold Spring Harbor Laboratory (http://www.cshl.edu)

 


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