BEZ235
BEZ235 (also known as Dactolisib) is a dual phosphoinositide 3-kinase/mTOR inhibitor that has been under investigation for its potential use in the treatment of various types of cancer. BEZ235 inhibits both the PI3K pathway and the mTOR pathway, which are often activated in cancer cells, leading to uncontrolled cell growth and survival. By targeting these pathways, BEZ235 aims to halt cancer cell proliferation and induce cell death.
Mechanism of Action[edit | edit source]
BEZ235 works by inhibiting the activity of a group of enzymes known as phosphoinositide 3-kinases (PI3Ks) and the mammalian target of rapamycin (mTOR). PI3Ks are involved in the signaling pathways that regulate cell growth, proliferation, survival, and angiogenesis. mTOR is a key protein within the PI3K pathway that further regulates cell growth and metabolism. By inhibiting these critical pathways, BEZ235 disrupts the processes essential for tumor growth and survival.
Clinical Trials[edit | edit source]
Several clinical trials have been conducted to evaluate the efficacy and safety of BEZ235 in various cancers, including breast cancer, advanced solid tumors, and renal cell carcinoma. While some trials have shown promise, the overall clinical benefit of BEZ235 remains to be fully established. The drug's effectiveness and safety profile continue to be areas of active research.
Adverse Effects[edit | edit source]
The administration of BEZ235 has been associated with a range of adverse effects. Commonly reported side effects include nausea, vomiting, diarrhea, fatigue, and hyperglycemia. As with many cancer therapies, the balance between efficacy and tolerability is a critical consideration in the ongoing development and potential clinical use of BEZ235.
Future Directions[edit | edit source]
Research into BEZ235 and other dual PI3K/mTOR inhibitors is ongoing, with scientists exploring the best ways to integrate these agents into cancer treatment regimens. This includes investigating BEZ235's use in combination with other therapies, its efficacy in specific cancer subtypes, and identifying biomarkers that predict response to treatment.
See Also[edit | edit source]
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Contributors: Prab R. Tumpati, MD