3-Methyladenine, often referred to as 3-MA, emerges as a diminutive molecule inhibitor targeting the protein PI3K (Phosphatidylinositol 3-kinase). PI3K, a signaling protein integral to cell growth, survival, and metabolism, often becomes hyperactive in cancer cells, fueling uncontrollable proliferation. By quelling PI3K, 3-MA has the capability to curb cancer cell growth and prompt cellular demise.
Specifically inhibiting class IA PI3Ks, constituted of a catalytic p110 subunit and a regulatory p85 subunit, 3-MA intervenes in the kinase activity of the PI3K p110 subunit, thus impeding its capacity to phosphorylate target proteins. Consequently, downstream signaling pathways instigated by PI3K, such as the Akt/mTOR pathway pivotal for cell survival and growth, are thwarted.
Beyond its potential in oncology, 3-MA showcases anti-inflammatory attributes. It dampens the production of pro-inflammatory cytokines like TNF-alpha and IL-6 and reduces the number of inflammatory cells. These qualities have prompted exploration into its application for inflammatory diseases like rheumatoid arthritis, multiple sclerosis, and inflammatory bowel disease.A Promising Tool for Cancer and Inflammation Therapy, this innovation holds significant potential for addressing complex medical challenges.
While undergoing preclinical and clinical assessments as a therapeutic agent for cancer and other diseases, 3-MA's preclinical studies have demonstrated its efficacy in restraining diverse cancer cell lines spanning breast cancer, lung cancer, and glioblastoma. It's also shown potential to amplify the impact of other cancer treatments like radiation therapy and chemotherapy.
However, its clinical trials remain at a nascent stage. The safety and efficacy of 3-MA as a viable treatment for cancer or other diseases are yet to be conclusively determined. It's vital to underline that comprehending 3-MA's mechanism of action and potential side effects necessitates further research before considering it a safe and potent solution for human diseases.
For more information, please visit here: https://www.glpbio.com/3-methyladenine.html
Specifically inhibiting class IA PI3Ks, constituted of a catalytic p110 subunit and a regulatory p85 subunit, 3-MA intervenes in the kinase activity of the PI3K p110 subunit, thus impeding its capacity to phosphorylate target proteins. Consequently, downstream signaling pathways instigated by PI3K, such as the Akt/mTOR pathway pivotal for cell survival and growth, are thwarted.
Beyond its potential in oncology, 3-MA showcases anti-inflammatory attributes. It dampens the production of pro-inflammatory cytokines like TNF-alpha and IL-6 and reduces the number of inflammatory cells. These qualities have prompted exploration into its application for inflammatory diseases like rheumatoid arthritis, multiple sclerosis, and inflammatory bowel disease.A Promising Tool for Cancer and Inflammation Therapy, this innovation holds significant potential for addressing complex medical challenges.
While undergoing preclinical and clinical assessments as a therapeutic agent for cancer and other diseases, 3-MA's preclinical studies have demonstrated its efficacy in restraining diverse cancer cell lines spanning breast cancer, lung cancer, and glioblastoma. It's also shown potential to amplify the impact of other cancer treatments like radiation therapy and chemotherapy.
However, its clinical trials remain at a nascent stage. The safety and efficacy of 3-MA as a viable treatment for cancer or other diseases are yet to be conclusively determined. It's vital to underline that comprehending 3-MA's mechanism of action and potential side effects necessitates further research before considering it a safe and potent solution for human diseases.
For more information, please visit here: https://www.glpbio.com/3-methyladenine.html
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