Press releases

New molecules discovered to tackle cancer resistance

27 Feb 2012 | By INSERM (Newsroom) | Cancer

A French-Italian team headed by researchers from CNRS and Inserm (1) has recently discovered a new family of compounds that could make it possible to treat numerous cancers, particularly brain tumours and skin cancers. These substances, patented by CNRS, block a chain of molecular reactions known as the Hedgehog signalling pathway, the disruption of which could be involved in several cancers. These compounds could become new medicines in the long term. In the short term, they should prove to be precious tools in elucidating the role of the Hedgehog pathway in the development of these tumours and their resistance to treatment. This work, carried out in collaboration with the Laboratoire d’Innovations Thérapeutiques (CNRS / Université de Strasbourg), is published in the Journal of Medicinal Chemistry.

The Hedgehog signalling pathway is a cascade of complex biochemical reactions. Very active during embryogenesis, it participates in cell proliferation and differentiation, as well as in the development of numerous tissues. In adults, it plays a key role, particularly in maintaining stem cells in the brain. The disruption of this pathway could participate in the development of many cancers, especially very aggressive brain tumours in children.

Malfunctions affecting the Hedgehog pathway can be caused by mutations of a membrane receptor known as Smoothened, an essential link permitting the activation of the Hedgehog pathway. Several pharmaceutical laboratories have developed compounds capable of blocking Smoothened. Thanks to these receptor antagonistic compounds (2), they have succeeded in stopping the development of certain tumours. However, experiments conducted on animal models and in humans demonstrate the onset of resistance to these treatments. New mutations of Smoothened in the tumoral cells annihilate the effects of the antagonists responsible for inactivating it. For this reason, it is important to find new antagonists and to better understand the mechanisms underlying this type of resistance.

In order to discover new Smoothened antagonists, the team of researchers coordinated by Martial Ruat adopted a novel strategy, namely the virtual screening of computerized molecular databases.

Among the 500,000 or so molecules included in these databases, they searched for those whose structure could produce the same effect as molecules already known to inhibit Smoothened. The scientists selected one molecule out of about 20 candidates. By slightly modifying its structure in order to optimize it, they discovered a family of compounds known as MRT and tested their biological activity on cultured mouse cells.The team discovered that MRT compounds, and more particularly acylguanidine MRT83, block the proliferation of cells suspected of causing brain tumours. In addition, these new compounds inhibit Smoothened with an activity similar to or exceeding that of already known compounds.

Several years of tests will be necessary before promising new substances such as MRT compounds can be marketed as medicines. Nevertheless, their properties could shed new light on the functioning, the three dimensional structure and the location of Smoothened receptors. These MRT compounds could contribute to understanding the cause of tumour resistance. This study could lead to the discovery of new targets and therapeutic strategies for combating certain cancers.


(1) In the ‘Neurobiology & development’ research unit (CNRS), in collaboration with the University of Sienna (Italy)

(2) When bound to the same cell receptors as one other substance, an antagonist substance blocks all or part of the effects normally produced by the cell. Here the receptor antagonist has an ‘inverse’ effect compared with that of the ‘muted’ receptor.

Researcher Contact
Martial Ruat tél. : 01 69 82 36 41
Press Contact
CNRS Priscilla Dacher tél. : 01 44 96 46 06
Acylthiourea, Acylurea and Acylguanidine Derivatives with potent Hedgehog inhibiting Activity Antonio Solinas, Hélène Faure, Hermine Roudaut, Elisabeth Traiffort, Angèle Schoenfelder, André Mann, Fabrizio Manetti, Maurizio Taddei and Martial Ruat. Journal of Medicinal Chemistry. 23 février 2012.