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New antivirals could help prevent cold sores by changing cell structures

A class of antivirals called Pin1 inhibitors could reduce or stop outbreaks of herpes simplex virus 1 (HSV-1), the common infection behind oral herpes, according to new research published in Antiviral Research.

HSV-1 causes sores around the mouth, commonly called cold sores or fever blisters. Most people are infected with HSV-1 in childhood, and between 50% and 90% of people worldwide have HSV-1. After the , HSV-1 remains in the body and can reactivate throughout a person’s life. While HSV-1 infections are usually mild, they can be serious and even deadly for people with suppressed immune systems. Finding new, more effective antivirals for this common illness is essential.

Researchers focused on an enzyme called peptidyl-prolyl cis-trans isomerase NIMA-interacting 1, or Pin1, that regulates protein stability, function, and cellular structure. When this is dysregulated, it can play a role in a variety of conditions, including obesity, cancer, , and more. Viruses, such as cytomegalovirus (CMV) and SARS-CoV-2, are known to affect Pin1, and Pin1 have been developed to reduce the impact of these viruses.

Role of hypoxia in cancer therapy by regulating the tumor microenvironment

Clinical resistance is a complex phenomenon in major human cancers involving multifactorial mechanisms, and hypoxia is one of the key components that affect the cellular expression program and lead to therapy resistance. The present study aimed to summarize the role of hypoxia in cancer therapy by regulating the tumor microenvironment (TME) and to highlight the potential of hypoxia-targeted therapy.

Sensor identifies sodium nitrite in drinks using laser-modified cork

A team of researchers from the Federal University of São Carlos (UFSCar) in the state of São Paulo, Brazil, has developed a sensor that can identify sodium nitrite (NaNO2) in various beverages, including mineral water, orange juice, and wine. This inorganic salt is used as a preservative and fixative to give products such as ham, bacon, and sausages their pink or red color. Depending on the amount, it can cause serious health problems by leading to the formation of nitrosamines, which are carcinogenic compounds.

“This risk motivated us to develop a simple, fast, and accessible way to detect the compound and ensure the quality and safety of liquid consumption,” says Bruno Campos Janegitz, head of the Laboratory of Sensors, Nanomedicine, and Nanostructured Materials (LSNano) at UFSCar. Janegitz coordinated the study, which was published in the journal Microchimica Acta.

“Detection [of NaNO2] in beverages, especially wines, is important for , since its use is not legally permitted in Brazil and most countries,” the authors write in the article.

Transparent wearable monitor gives real-time warnings about overexposure to sunlight

Scientists in South Korea have unveiled a transparent, wearable sensor that monitors a user’s exposure to ultraviolet A (UVA) radiation in real-time. The technology could help prevent sunburn and long-term skin damage that can cause cancer.

Ultraviolet radiation is released naturally by the sun and artificially by tanning beds. The problem with overexposure is that the rays can penetrate deep into the skin and damage DNA, potentially causing cells to grow out of control and leading to cancer. In many countries, the majority of skin cancer cases are linked to this type of overexposure.

While wearing long clothes and hats and applying sunscreen provides valuable protection, the researchers wanted a simple device to alert wearers when exposure reached a certain level. Current sensors often lack the ability to track UVA and are opaque, which makes them uncomfortable and difficult to use in wearable tech like smart glasses.

Developing drugs—with tens of thousands of minuscule droplets on a small glass plate

A glass plate, a delicate tube and an oil bath are all that is required: thanks to a new method, researchers at ETH Zurich can produce tens of thousands of tiny droplets within minutes. This enables them to test enzymes and active ingredients faster, more precisely and in a more resource-efficient manner than previously.

What happens when an enzyme encounters a potential active ingredient that is supposed to inhibit or activate the enzyme? This is precisely what drug development is all about. Analyzing the interaction of an enzyme with an active ingredient molecule, however, is extremely complex.

The group led by Petra Dittrich, Professor of Bioanalytics at ETH Zurich, has developed a method that radically simplifies such tests: their method allows up to 100,000 minuscule droplets containing enzymes and substrates to be produced on a glass plate—in a mere 40 minutes and without involving a pipette.

Deep sleep supports memory via brain fluid and neural rhythms, research finds

Researchers led by Masako Tamaki at the RIKEN Center for Brain Science in Japan report a link between deep sleep and cerebrospinal fluid, the clear liquid that surrounds and supports the brain and spinal cord. Published in Proceedings of the National Academy of Sciences, the study demonstrates how changes in cerebrospinal fluid signals during sleep—as measured by MRI—are time-locked to slow brain waves and other neural events.

These findings offer a clue as to why stable sleep is important for normal brain function, particularly within the brain network that controls learning and memory.

Why do we sleep? Scientists think that sleep is important for consolidating memories and removing waste from the brain that accumulates as a result of brain activity while we are awake.

Cambridge lab-grown human embryo model produces blood cells

Prof Azim Surani, senior author of the paper, said: “Although it is still in the early stages, the ability to produce human blood cells in the lab marks a significant step towards future regenerative therapies — which use a patient’s own cells to repair and regenerate damaged tissues.”

Human blood stem cells, also known as hematopoietic stem cells, are immature cells that can develop into any type of blood cell.

These include red blood cells that carry oxygen and various types of white blood cells crucial to the immune system.

Surprising gene mutation in brain’s immune cells linked to increased Alzheimer’s risk

In a study published in Neuron, a research team at the Department of Neurology at Massachusetts General Hospital, aimed to understand how immune cells of the brain, called microglia, contribute to Alzheimer’s disease (AD) pathology. It’s known that subtle changes, or mutations, in genes expressed in microglia are associated with an increased risk for developing late-onset AD.

The study focused on one such mutation in the microglial gene TREM2, an essential switch that activates microglia to clean up toxic amyloid plaques (abnormal protein deposits) that build up between in the brain. This mutation, called T96K, is a “gain-of-function” mutation in TREM2, meaning it increases TREM2 activation and allows the gene to remain super active.

The researchers explored how this mutation impacts microglial function to increase risk for AD. The team generated a mutant mouse model carrying the mutation, which was bred with a mouse model of AD to have brain changes consistent with AD. They found that in female AD mice exclusively, the mutation strongly reduced the capability of microglia to respond to toxic amyloid plaques, making these cells less protective against brain aging.

Large language models prioritize helpfulness over accuracy in medical contexts, finds study

Large language models (LLMs) can store and recall vast quantities of medical information, but their ability to process this information in rational ways remains variable. A new study led by investigators from Mass General Brigham demonstrated a vulnerability in that LLMs are designed to be sycophantic, or excessively helpful and agreeable, which leads them to overwhelmingly fail to appropriately challenge illogical medical queries despite possessing the information necessary to do so.

Findings, published in npj Digital Medicine, demonstrate that targeted training and fine-tuning can improve LLMs’ abilities to respond to illogical prompts accurately.

“As a community, we need to work on training both patients and clinicians to be safe users of LLMs, and a key part of that is going to be bringing to the surface the types of errors that these models make,” said corresponding author Danielle Bitterman, MD, a faculty member in the Artificial Intelligence in Medicine (AIM) Program and Clinical Lead for Data Science/AI at Mass General Brigham.

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