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- Combines thymosin beta 4 with chemotherapy/radiation to target medulloblastoma and glioblastoma with high p53 levels.
- Enhances cancer cell targeting while minimizing damage to normal cells, improving treatment outcomes and patient safety.
- Applicable for both pediatric and adult brain cancers, offering a versatile approach to difficult-to-treat tumors.
OVERVIEW
This invention provides a novel method to enhance chemotherapy for treating medulloblastoma and glioblastoma characterized by high basal p53 levels. It involves the use of a PI3K activator, such as thymosin beta 4, in combination with traditional chemotherapy and/or radiation. This innovative approach improves the effectiveness of cancer treatments by targeting cancer cells more precisely while reducing adverse effects on normal cells. For example, thymosin beta 4 can be administered with a chemotherapeutic agent to medulloblastoma patients, leading to increased treatment efficacy and reduced neurocognitive side effects.
BACKGROUND
Medulloblastoma is the most common malignant brain tumor in children, requiring aggressive treatment involving surgery, radiation, and chemotherapy. Glioblastoma is the most prevalent brain cancer in adults, notorious for its poor prognosis despite intensive treatment. Current therapies often result in significant side effects and limited effectiveness, especially for tumors with high p53 levels. This invention addresses these challenges by enhancing the effectiveness of chemotherapy and reducing damage to healthy cells.
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Our mission is to advance GU’s innovations through strategic alliances and new venture creation, to facilitate the translation of research breakthroughs into tangible solutions, and to cultivate a dynamic and inclusive environment for entrepreneurship. We advance this mission in support of the GU community and for the benefit of society.
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