Researchers in Canada have come across a novel mechanism that may be instrumental in the development of new, more effective cancer therapies.
They have discovered that activation mechanism of the RAF protein kinase which, when mutated, is responsible for more than 25 per cent of cancers.
Understanding this mechanism may lead to novel anti-cancer agents designed to minimize the toxic side effects caused by chemotherapy.
Marc Therrien at the Institute for Research in Immunology and Cancer (IRIC) of the Universiti de Montrial, and Frank Sicheri, at the Samuel Lunenfeld Research Institute of Mount Sinai Hospital in Toronto claim that dimerization, or combination, of two RAF proteins is essential to its activation.
Inhibiting the dimerization of RAF may therefore block its activation, thus stopping cancer cells from growing.
The study exposes not only the activation mechanism of RAF, but potentially the mechanisms that control other protein kinases, a large number of which are linked to cancer and other diseases such as diabetes, hypertension and neurodegeneration.
"Basic researchers believe that one of the most promising strategies to finding lifelong cures for cancers lies in understanding the molecular underpinnings specific to cancer cells," Nature quoted Therrien as saying.
"It is hoped that this will translate to the development of inhibitors tailored to specific molecular defects and, as a result, should increase the effectiveness of new target-based cancer therapies," he added.
Sicheri said, "protein kinases are the targets for some of the most successful anti-cancer drugs in the clinic."
"Now that we have discovered how to turn off the RAF protein without interfering with other proteins, we may be able to design drugs that have unprecedented precision in targeting cancer cells while reducing the toxic side effects for patients," he added.