Innovative research shows that cancer cell survival can be compromised by protecting, activating, and accumulating essential genes. PearlsInMires develops next-generation anti-cancer drugs offering sustained effects and freedom from resistance and toxicity.
Target protection and activation can induce unique mechanisms that make cancer cells more perform their inherent functions. Since the mechanisms that drive aggressive growth in cancer cells are distinct from the functions of normal cells, this approach specifically targets cancer cells, resulting in minimal toxicity.
For cancer cells to respond to target activation, they must suppress target expression on their own. If the cancer-specific action is spontaneously reduced, it becomes free from anti-cancer drug resistance and allows the acquisition of normal cell characteristics.
A comprehensive approach to cancer genetics is essential for predicting best targets in drug development. New analytical methods have provided evidence that activating certain cancer pathways can induce vulnerabilities in cancer cell survival.
Clinical studies on resistance to existing inhibitors have shown that some cancers regress when the inhibitor is discontinued. This suggests that the anti-cancer effect may be induced by activating specific targets within cancer cells.
Inhibition of the intrinsic mechanism possessed by cancer cells continuously induces several stages of regulatory mechanisms to escape from the inhibitors. Even under these regulations, various protective and hyperactive actions are prepared to ensure the correct level of cellular activity.
Drugs are administered to protect, activate, and accumulate targets essential for survival, thereby inducing the selective death of cancer cells. The protection and activation method involves disrupting the targets degrading mechanism by driving materials reconstructing the endogenous peptide.