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New therapeutic method combined with synthetic CDK4/6 inhibitors for refractory cancers

The RB1 tumor suppressor gene protein antagonizes uncontrolled growth of cancer by suppressing cell cycle progression but its function is repressed in most cancers. CDK4/6 represses this function by phosphorylating RB1. In contrast, drugs that inhibit CDK4/6 inhibit the phosphorylation of RB1 and restore the cancer-suppressing function of RB1. However, avis kamagra 100mg since it was difficult to achieve a sufficient therapeutic effect by a single administration of a synthetic CDK4/6 inhibitor, development of a combination therapy that maximizes the function of the drug has been awaited.

The research team led by Prof. Chiaki Takahashi of the Cancer Research Institute, Kanazawa University, in collaboration with a research team led by Associate Prof. Itsuki Ajioka of Tokyo Medical Dental University and with scientists from several domestic and overseas institutions found that hepatocellular carcinoma is generated due to loss of RB1 function in mouse hepatocytes. Then, they established cell lines such as hepatocellular carcinoma into which a mutation that mimics a state in which RB1 is constantly activated was introduced, and performed high-throughput screening in order to find a compound that enhances the effect of a synthetic CDK4/6 inhibitor. As a result, they found that an IKKβ inhibitor shows such an effect. This weakens the function of IKKβ kinase and allows cells to escape from cell death. It was found that when treated with a synthetic CDK4/6 inhibitor alone, IKKα/β and its downstream NF-κB, which detect abnormalities triggered by nucleic acid synthesis deficiency, were activated to avoid cell death, causing insufficient therapeutic effects. Next, they performed similar analyses for K-Ras oncogene mutated lung cancer and colorectal cancer having intact RB1 and found that combined use of another drug that inhibits another kinase, AKT, is effective in a way similar to that obtained by combined use of an IKKβ inhibitor.


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