A new Met inhibitory-scaffold identified by a focused forward chemical biological screen.

Abstract : The receptor tyrosine kinase Met is crucial for the genetic program causing cancer progression and metastasis. Its nodal function during aggressiveness and resistance acquisition poses Met inhibition as an obligatory step in anti-cancer targeted therapy. Here, we applied a “Met-focussed” forward chemical biological screen to discover new agents antagonizing Met-triggered biological functions. The identified new scaffold, JLK1360, has a dual mechanism of action towards Met: it impairs Met signalling and also prevents its restoration after degradation. Docking and molecular dynamics provide evidences on the interacting mode of JLK1360 within the Met ATP-binding pocket. Moreover, computational and biochemical studies also highlighted that JLK1360 has a good degree of selectivity towards Met than other RTKs tested. Altogether, these findings demonstrate that the approach we have applied is a powerful strategy to identify compounds with combined properties towards a chosen target. Our studies show how integration of chemistry, biology and computational analysis can provide robust strategies to identify new inhibitory scaffolds suitable for further development of anti-cancer targeted therapies.
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Article dans une revue
Biochemical and Biophysical Research Communications, Elsevier, 2008, 375 (2), pp.184-189
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https://hal.inria.fr/inria-00339127
Contributeur : Malika Smail-Tabbone <>
Soumis le : dimanche 16 novembre 2008 - 23:13:17
Dernière modification le : jeudi 18 janvier 2018 - 02:31:02

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  • HAL Id : inria-00339127, version 1

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Salvatore Patané, Nicolas Pietrancosta, Hessameh Hassani, Vincent Leroux, Bernard Maigret, et al.. A new Met inhibitory-scaffold identified by a focused forward chemical biological screen.. Biochemical and Biophysical Research Communications, Elsevier, 2008, 375 (2), pp.184-189. 〈inria-00339127〉

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