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Cancer: Treatment that prevents tumor metastasis identified in animal study

Date:
July 24, 2014
Source:
Université catholique de Louvain - UCL
Summary:
Metastasis, the strategy adopted by tumor cells to transform into an aggressive form of cancer, are often associated with a gloomy prognosis. Managing to block the metastasis or, even better, prevent their formation would be a giant step towards the fight against cancer. Researchers successfully performed this on models of human tumors in mice.
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Metastasis, the strategy adopted by tumor cells to transform into an aggressive form of cancer, are often associated with a gloomy prognosis. Managing to block the metastasis or, even better, prevent their formation would be a giant step towards the fight against cancer. Researchers at Université catholique de Louvain (Belgium) successfully performed this world first on models of human tumors in mice. The results of their study are published online on 24 July in the journal Cell Reports.

The work by Professor Pierre Sonveaux's team, at Université catholique de Louvain's Institute of Experimental and Clinical Research (IREC), succeeded in pinpointing a family of pharmaceutical compounds whose action prevents the appearance of tumor metastasis. The researchers achieved this tour de force by studying the mitochondria in tumor cells. These organelles are considered as the cells' power station. But when their functioning is altered, as the UCL researchers observed in tumor cells, the mitochondria can promote cell migration, thus leading to the formation of metastasis.

Paolo E. Porporato, a post-doctoral researcher, and other young researchers in Professor Pierre Sonveaux's team, examined the molecular mechanism responsible for the mitochondria's ability to promote metastasis. They succeeded in showing that, under certain conditions, the mitochondria produce more free radicals known as superoxide ions (O2.-). It is this overproduction of superoxide that leads to the formation of metastasis and, consequently, the growth of a tumor.

Involved in other human pathologies such as Parkinson's and Alzheimer's disease, the production of superoxide by the mitochondria can be blocked by very specific antioxidants such as MitoTEMPO. Used in models of murine and human tumors, these compounds turned out to be very efficient at blocking the migration of tumor cells and preventing the spontaneous formation of human tumor metastasis in mice!

This research was conducted within the framework of projects mainly financed by an ERC Starting Grant, which Pierre Sonveaux obtained in 2009, and support from the F.R.S.-FNRS, Télévie and the Fondation contre le Cancer. The discovery of a treatment capable of blocking the mechanism responsible for the formation of metastasis and the existence of a family of promising compounds, is encouragement for their future assessment in a clinical study that aims to validate a preventive treatment against tumor metastasis.


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Materials provided by Université catholique de Louvain - UCL. Note: Content may be edited for style and length.


Journal Reference:

  1. Paolo E. Porporato, Valéry L. Payen, Jhudit Pérez-Escuredo, Christophe J. De Saedeleer, Pierre Danhier, Tamara Copetti, Suveera Dhup, Morgane Tardy, Thibaut Vazeille, Caroline Bouzin, Olivier Feron, Carine Michiels, Bernard Gallez, Pierre Sonveaux. A Mitochondrial Switch Promotes Tumor Metastasis. Cell Reports, 2014; DOI: 10.1016/j.celrep.2014.06.043

Cite This Page:

Université catholique de Louvain - UCL. "Cancer: Treatment that prevents tumor metastasis identified in animal study." ScienceDaily. ScienceDaily, 24 July 2014. <www.sciencedaily.com/releases/2014/07/140724124256.htm>.
Université catholique de Louvain - UCL. (2014, July 24). Cancer: Treatment that prevents tumor metastasis identified in animal study. ScienceDaily. Retrieved March 28, 2024 from www.sciencedaily.com/releases/2014/07/140724124256.htm
Université catholique de Louvain - UCL. "Cancer: Treatment that prevents tumor metastasis identified in animal study." ScienceDaily. www.sciencedaily.com/releases/2014/07/140724124256.htm (accessed March 28, 2024).

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