Ongoing Battle: Latest Updates & Cutting-Edge Research in Brain Cancer
Lance Kawaguchi
Global Finance, Sustainability and Nonprofit Leader I Chief Executive Officer | Multi-Board Chairman | Strategic Advisor
A Novel MDM2 Inhibitor?
In many cancers, including glioblastoma (GBM), the tumour suppressor gene p53
(Tp53) is frequently mutated, and its downstream regulators are often inactivated. This can result in amplification and overexpression of oncoproteins such as MDM2. Essentially, MDM2 acts as a brake on p53, preventing it from doing its job effectively. Researchers from Canada tested the efficacy of the MDM2 inhibitor, BI-907828, in GBM patient-derived brain tumour stem cells (in vitro and in orthotopic xenograft models). It was shown that BI-907828 crosses the blood-brain barrier and treatment resulted in tumour death and an increase in survival. It was concluded that BI-907828 provides a promising novel therapeutic option for patients with TP53 wild-type primary brain tumours and that there is a strong rationale to translate it to the clinic for testing.
Genetically Engineered Treatments?
Purdue University researchers are developing and validating a patent-pending treatment for GBM. Essentially, the team is developing a type of immunotherapy based on novel, genetically engineered, fully off-the-shelf, or allogeneic immune cells (cells from a source that is not the patient). The research team tested their novel therapy in a preclinical setting by direct injection of the newly engineered immune cells into mice bearing human brain tumours. Results showed the immune cells to be highly effective in targeting and eliminating the growth of the tumours. Such results hold promise in translating to clinical trials with the team adding they are working with neurosurgical clinician collaborators to not only obtain funding, but also initiate clinical protocols.
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References
BI-907828, a novel potent MDM2 inhibitor, inhibits glioblastoma brain tumor stem cells in vitro and prolongs survival in orthotopic xenograft mouse models - PMC (nih.gov )
synNotch-programmed iPSC-derived NK cells usurp TIGIT and CD73 activities for glioblastoma therapy | Nature Communications
Disclaimer: Information in this article is sourced from published articles; readers are advised to independently verify facts. Opinions expressed are the author's own and do not necessarily reflect those of the publisher. If you experience symptoms related to brain cancer, consult with a medical professional for personalised advice and guidance.
Founder/ CEO at Praesidia Biotherapeutics, Co-founded and exited as CEO of Inbiopro and Zumutor Biologics, brought specialized probiotics to market
5 个月Lance, couldn't agree more. Brain cancer in particular, and CNS therapies in general, remain an area of unmet clinical need. It is not so much the lack of efficacious drugs, but being able to get them across the blood-brain barrier (BBB) in a clinically relevant level remains a major bottleneck. Often, trying to push through enough drugs results in dose-limiting systemic toxicity. We are excited at the prospect of Praesidia's linker technology (Linker Enzyme Substrate System) to actively transport drugs across the BBB, while also increasing the maximum tolerable dose, solving this major bottleneck.
Passionate about raising awareness and funds for vital Brain Cancer research to save lives. Cure Brain Cancer Advocate ?? Grieving Mother ?? Wife ??♀? OAM???
5 个月Thx for sharing this update Lance Every piece of the puzzle (information) that we find is valuable and a step closer to better understanding of this disease which ultimately will lead to better treatments and outcomes for patients.
Brain Cancer Ambassador Human Resources Professional
5 个月Thank you Lance Kawaguchi for bringing this to light for us!! It is so promising to hear the work our brilliant researchers are doing and continue to do to find a cure!! We are blessed to have amazing minds that dedicate their lives to finding a cure for this horrible disease ??
Chairman at Blackrun Partners
5 个月Thanks for all you Lance Kawaguchi and all at Cure Brain Cancer Foundation do everyday to advance research and potential cures for this terrible disease