Neuromics

🧬 New graduates step forward to advance cancer research

Neuromics congratulates Magdalena Murray and Santiago Sanchez

https://tinyurl.com/Cancer-Research-Stanford

"Cancer is often treated only after it becomes visible. But some of the most important discoveries happen earlier, at the cellular level, where the molecular processes that drive health and disease first unfold."

✅ "Magdalena Murray, PhD, and Santiago Sanchez, MD, PhD candidate, have spent years working in this critical space. Murray aims to kill cancer cells by exploiting their vulnerabilities. Sanchez hopes to improve early detection and prevention by understanding how a critical chromosome structure is linked to disease. Though they ask different questions, both are working to uncover new ways to combat cancer."
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New graduates step forward to advance cancer research The Stanford Cancer Biology PhD Program is preparing the next generation of scientists to tackle some of cancer research’s most challenging questions.

🛄 Neuromics (www.neuromics.com) Organoid Induction, Growth, and Maintenance Media
🟩 Organoids offer researchers 3D, self-assembling cellular clusters that mimic the architecture and functionality of real human organs. They bridge the gap between traditional 2D cell cultures and living animal models, allowing for more accurate, human-specific testing.

▶️ Neuromics Organoid Media are chemically defined, serum-free, animal component–free media optimized and formulated to support the self-organization of endothelial cells, pericytes, and mesenchymal cells into complex 3D structures that recapitulate the architecture and function of human blood vessels, including capillary networks and
arteriole-like structures.
https://www.neuromics.com/organoid-induction-growth-and-maintenance-media

🛄 Neuromics (www.neuromics.com) Organoid Induction, Growth, and Maintenance Media
🔷 Organoids offer researchers 3D, self-assembling cellular clusters that mimic the architecture and functionality of real human organs. They bridge the gap between traditional 2D cell cultures and living animal models, allowing for more accurate, human-specific testing.

▶️ Neuromics Organoid Media are chemically defined, serum-free, animal component–free media optimized and formulated to support the self-organization of endothelial cells, pericytes, and mesenchymal cells into complex 3D structures that recapitulate the architecture and function of human blood vessels, including capillary networks and arteriole-like structures.

Organoid Induction and Growth Media Neuromics, Vascular Organoid Media is designed to induce and grow physiologically relevant blood vessel organoids—easily and with high yield—for your tissue repair and regeneration studies or to model vascular disease in vitro. The media drives efficient and reproducible generation of blood vess...

Courtesy of RFK, jr's, Centers for Disease Control and Prevention, and U.S. Department of Health and Human Services (HHS) vaccine propaganda.
https://tinyurl.com/RFK-JR-MEASLES-UTAH
"While most recover, some — particularly young babies, pregnant people, and those with weak immune systems — are at higher risk of developing dangerous complications such as pneumonia, brain swelling, blindness, or even death. Even healthy people can develop issues years down the road, including a rare but fatal degenerative brain disease that can manifest about a decade after infection."

"The measles vaccine is safe and 97% protective after two doses."

Interesting results courtesy of Shining Science
This is a pre-clinical study. Hope? Yes. Clinical studies required.
📰 source: Murdock, M. H., et al. Multisensory gamma stimulation promotes glymphatic clearance of amyloid. Nature, 627(8002), 149-156.
Highlights:
🧠 A noninvasive treatment using light and sound shown to trigger the brain’s natural waste-clearance system to combat Alzheimer's disease.
✅ In a groundbreaking preclinical study funded by the National Institute on Aging (NIA), researchers from MIT, Boston University, and Westlake University in China have discovered that noninvasive light and sound stimulation can significantly reduce levels of toxic amyloid proteins in the brain.
✅ This sensory stimulation effectively tapped into the brain’s glymphatic system—its internal waste-disposal network—prompting cells called astrocytes to expand, flush out debris, and clear the destructive plaques historically associated with Alzheimer’s disease.
➡️ These promising results suggest that simple, noninvasive sensory therapy could act as a potent tool to keep our brain's plumbing running smoothly, offering a highly accessible avenue for treating Alzheimer’s and other protein-accumulating neurological disorders.
Stay tuned.. Neuromics will stay informed as noninvasive therapies move into Clinical Studies.
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📰Neuromics' Pancreatic CAFS used in Phase 1 Trial

➡️ Adenosine Biology and Pancreatic Cancer and Tumor Microenvironment (TME)

✅ Researchers from Arcus Biosciences, UCLA, Columbia, Stephenson Cancer Center, MD Anderson Cancer Center, Sarah Cannon Research Institute, University of Wisconsin, and NYU Langone used Neuromics' Pancreatic Cancer-Associated Fibroblasts (CAFS) https://neuromics.com/CAF118 to conduct a Phase 1 Study.

"Quemliclustat and chemotherapy with or without Zimberelimab in metastatic pancreatic adenocarcinoma: a randomized phase 1 trial."
https://nature.com/articles/s41591-026-04283-z

🧬 Image: a, Venn diagrams showing genes upregulated via RNA-seq experiments in four cell types comprising components of the TME (PANC-1, MIA PaCa-2, CAF, and CD8+ T cells) and inhibited in two cell types (PANC-1 and MIA PaCa-2). A total of 15 genes were upregulated by AMP and inhibited by quemliclustat. Differentially expressed genes are defined as an increase or decrease of 50% log2 fold change with FDR ≤ 0.05. b, Heatmap of log2 fold change of RT−PCR values for NR4A family genes treated with adenosine-generating conditions or adenosine 2a receptor/adenosine 2b receptor agonist conditions and their corresponding inhibitors in expanded cell types in the TME. c, NR4A family genes can be upregulated to varying degrees in cell types compared to human PDAC in response to chemotherapy.

Elevated adenosine levels in the TME suppress inflammation and immune function, markedly limiting the ability of the immune system to destroy tumor cells.