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Abstract: Stressing the details in the link between chronic stress and liver cancer…

Here, Xuetian Yue discover chronic stress promotes aminopeptidase N expression to increase glutathione synthesis and inhibit ferroptosis in models of liver cancer.


1Department of Cellular Biology, School of Basic Medical Sciences;

2Key Laboratory for Experimental Teratology of Ministry of Education and Department of Immunology, School of Basic Medical Sciences; and.

3Key Laboratory for Experimental Teratology of the Ministry of Education, Department of Histology and Embryology, School of Basic Medical Sciences, Cheeloo Medical College, Shandong University, Jinan, China.

Abstract: Opening the gates to the blood brain barrier (BBB) in a high-grade glioma model

Amy B. Heimberger find therapeutic benefit in adding the STING agonist 8,803 to radiation in preclinical models of glioma. The combination reprogramed the glioma tumor microenvironment, and 8,803 induced the opening of the blood-brain barrier.


3Department of Radiology.

4Department of Neurology, and.

5Department of Radiation Oncology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.

Tumour–brain crosstalk restrains cancer immunity via a sensory–sympathetic axis

Tumor–brain crosstalk worsens lung cancer.

It is not clear how the brain senses and responds to tumors in peripheral organs, although tumors are innervated by different branches of the peripheral nervous system and increased tumor innervation is associated with poor cancer outcomes.

Authors in this study identify an immuno-suppressive tumor microenvironment established by a tumor–brain axis that promotes oncogenesis.

The researchers demonstrate that lung adenocarcinoma induces innervation and functional engagement of vagal sensory neurons. Mechanistically, the vagal sensory nerves transmit signals from lung tumors to brainstem nuclei, driving elevated sympathetic efferent activity in the tumor microenvironment. This, in turn, suppresses β2 adrenergic signalling in alveolar macrophage and anti-tumor immunity.

Disruption of this sensory-to-sympathetic pathway significantly inhibited lung tumor growth by enhancing immune responses against cancer. sciencenewshighlights sciencemissionn https://sciencemission.com/Tumour%E2%80%93brain-crosstalk


Mouse models demonstrate that vagal sensory neurons transmit signals from lung adenocarcinoma to the brain, increasing sympathetic efferent activity in the tumour microenvironment and thereby creating a immunologically permissive environment for tumour growth.

Researchers pioneer next-generation AI semiconductors with ‘thermal constraining’ technique

A research team led by Professor Taesung Kim from the School of Mechanical Engineering at Sungkyunkwan University has developed a technology that precisely controls the internal structure of semiconductors using heat, much like stamping out “bungeoppang” (fish-shaped pastry) in a mold. The team report that this approach improves the performance of next-generation artificial intelligence (AI) hardware. With this technology, complex AI computations can be processed more quickly using significantly less electricity than before. The findings are published in the journal ACS Nano.

Most computers and smartphones we use today operate based on the “von Neumann architecture.” This structure is similar to having a desk (the processor) and a bookshelf (the memory) placed far apart.

Each time you study, you have to go back and forth to get a book, which takes time and effort. To solve this problem, a method called “in-memory computing” has been proposed, in which computation is carried out directly inside the memory. The key component that enables this approach is the “ferroelectric transistor,” which is the focus of this study.

Feedback neurons based on perovskite memristor with nickel single-atom engineered reduced graphene oxide cathode

Scientists have long looked to the human brain as the ultimate blueprint for computing, seeking to build “neuromorphic” systems that process information with the same efficiency and flexibility as our own neurons. However, replicating the brain’s complex ability to both excite and inhibit signals—essentially “talking” and “listening” simultaneously—has proven difficult with standard hardware.

The problem? Perovskites are often too chaotic. Tiny charged particles called ions tend to zip around inside the material too quickly, making the device’s behavior hard to control. Additionally, the “bottlenecks” (barriers) where the electricity enters the device often cause lopsided performance, preventing the smooth, bidirectional communication required for advanced brain-like tasks.


Li et al. report feedback neurons based on perovskite memristors with a nickel single-atom modified reduced graphene oxide cathode. The device successfully implements an unsupervised learning network with over 50% clustering accuracy and cooperative learning for solving NP-hard combinatorial optimisation problem.

Nobel Prize in Physics 1903

The Nobel Prize in Physics 1903 was divided, one half awarded to Antoine Henri Becquerel “in recognition of the extraordinary services he has rendered by his discovery of spontaneous radioactivity”, the other half jointly to Pierre Curie and Marie Curie, née Skłodowska “in recognition of the extraordinary services they have rendered by their joint researches on the radiation phenomena discovered by Professor Henri Becquerel”

How dietary restriction rewires immunity to protect against infection

To understand the complex interactions involved in an immune response during scarcity, the team put mice on a 50% restricted-calorie diet and then exposed the animals to bacteria that infect the gut. The mice that were fed a standard diet experienced a metabolic crash— their blood glucose levels and body weight plummeted.

The researchers had expected this would happen to all the animals because mounting an immune response can consume up to 30% of the entire body’s fuel reserves. But in the calorie-restricted mice, the immune system appeared to be functioning perfectly well without using much glucose.

To unravel this enigma, the researchers inventoried the immune cells of the infected animals and discovered that T cells, which normally target invading microbes, were depleted in the calorie-restricted mice. Instead, short-lived neutrophils, which serve as the body’s first responders to infection, were ramped up to twice the normal amount and had measurably enhanced pathogen-killing abilities. The cells seemed to be operating in energy-saving mode, consuming much less glucose than neutrophils from well-fed animals.

The researchers are breaking new ground by outlining how a sudden fall in food intake triggers glucocorticoid levels to rise, resulting in two major shifts. First, the body repositions certain immune cells—especially naïve T cells—into the bone marrow, which becomes a kind of “safe house” for when the cells are needed. Second, during an infection, glucocorticoids tilt the immune response away from energy-intensive T cells toward neutrophils, abundant cells that act as immediate, short-lived defenders.

Beyond clearing a current infection, glucocorticoids prepare the immune system for repeat encounters with infectious agents. While the hormones direct killer T cells to stand down and neutrophils to step up, they also ensure memory T cells are preserved for future confrontations.


When food is scarce, stress hormones direct the immune system to operate in “low power” mode to preserve immune function while conserving energy, according to researchers. This reconfiguration is crucial to combating infections amid food insecurity.

NAD+ sensing by PARP7 regulates the C/EBPβ-dependent transcription program during adipogenesis

Stokes et al. demonstrate that PARP7 “senses” the levels of nuclear NAD+ during early adipogenic differentiation via an ADP-ribosylation-ubiquitin-proteasome pathway to regulate C/EBPβ-dependent proadipogenic gene expression through p300-mediated H3K27 acetylation. Stabilized PARP7 promotes the binding of C/EBPβ to chromatin genome-wide, enhancing lipid synthesis and adipogenesis in vivo.

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