People seek NHS advice on drinking and breastfeeding at Christmas

Any alcohol that the mother drinks can pass into her breastmilk, the NHS advises.

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New drug to prevent migraine may start working right away

A drug recently approved to prevent migraine may start working right away, according to a study published in the December 23, 2024, online issue of Neurology®, the medical journal of the American Academy of Neurology. The study looked at the drug atogepant, which is a calcitonin gene-related peptide (CGRP) receptor antagonist taken by mouth.

“With many current drugs to prevent migraine, it takes time to find the right dosage for the individual and it can take weeks or even months for it to be most effective,” said study author Richard B. Lipton, MD, of Albert Einstein College of Medicine in the Bronx, New York, and a Fellow of the American Academy of Neurology. “Some people give up and stop taking the drugs before they reach this point. Plus, many people experience side effects with current treatments. Developing a drug that works both effectively and quickly is critical.”

In the study, people taking the drug atogepant were less likely to have a migraine on the first day of taking the drug compared to those taking a placebo. They also had fewer migraines per week during each of the first four weeks of the study and fewer migraines during the study overall than those taking a placebo.

For this study, researchers looked at the data from three trials on the safety and effectiveness of atogepant over 12 weeks to focus on how rapidly improvements appeared. The ADVANCE trial, which enrolled people with episodic migraine, had 222 people taking the drug and 214 taking placebo. The ELEVATE trial, which enrolled people with episodic migraine who had previously not responded well to other oral preventive treatments, had 151 on the drug and 154 on placebo. The PROGRESS trial, which enrolled people with chronic migraine, had 256 on the drug and 246 on placebo.

People with episodic migraine experience up to 14 migraine days per month. People with chronic migraine experience at least 15 days with headache per month, with at least eight days being characteristic of migraine.

On the first day of the study, 12% of those taking the drug in the first trial, the ADVANCE trial had a migraine, compared to 25% of those taking placebo. In the second trial, the ELEVATE trial, the numbers were 15% and 26%. For the third trial, the PROGRESS trial, the numbers were 51% and 61%.

When researchers adjusted for other factors that could affect the rate of migraine, they found that people taking the drug were 61% less likely to have a migraine in the first trial, 47% less likely in the second trial, and 37% less likely in the third trial.

For the first two trials, the people taking atogepant had an average of one fewer day with migraine per week, compared to an average of less than one-half day fewer per week for those taking the placebo. For the third trial, average migraine days per week declined by about 1.5 days for those taking the drug compared to about one day for those taking the placebo.

The people taking atogepant also showed improvement on assessments of how much migraine impaired their activities and their overall quality of life compared to people taking the placebo.

“Migraine is the second-leading cause of disability in the overall population and the leading cause of disability in young women, with people reporting negative effects on their relationships, parenting, career and finances,” Lipton said. “Having a treatment that can act quickly and effectively addresses a key need.”

A limitation of the study is that it involved mostly female and white participants, so the results may not apply to the overall population.

The study was supported by AbbVie, the maker of atogepant.

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Gene editing tool reduces Alzheimer’s plaque precursor in mice

A new gene editing tool that helps cellular machinery skip parts of genes responsible for diseases has been applied to reduce the formation of amyloid-beta plaque precursors in a mouse model of Alzheimer’s disease, researchers at the University of Illinois Urbana-Champaign report.

The application in live mice shows the improved efficiency of the tool, called SPLICER, over the current standard in gene editing technology, as well as the potential for application in other diseases, the researchers said. Led by Pablo Perez-Pinera, a professor of bioengineering at the U. of I., the researchers published their findings in the journal Nature Communications.

SPLICER uses a gene editing approach called exon skipping, which is of particular interest for health conditions caused by mutations that produce misfolded or toxic proteins, such as Duchenne’s muscular dystrophy or Huntington’s disease.

“DNA contains the instructions to build everything that is responsible for how cells function. So it’s like a book of recipes that contains very detailed instructions for cooking,” Perez-Pinera said. “But there are large regions of DNA that don’t code for anything. It’s like, you start the recipe for a turkey dinner, and then you hit a note that says, ‘continued on page 10.’ After page 10, it’s ‘continued on page 25.’ The pages between are gibberish.

“But say on one of the recipe pages — in genetics, an exon — there is a typo that makes the turkey inedible, or even poisonous. If we cannot correct the typo directly, we could amend the note before it to send you to the next page, skipping over the page with the error, so that at the end you could make an edible turkey. Though you might lose out on the gravy that was on the skipped page, you’d still have dinner. In the same way, if we can skip the piece of the gene with the toxic mutation, the resulting protein could still have enough function to perform its critical roles.”

SPLICER builds upon the popular CRISPR-Cas9 gene editing platform — with key changes. CRISPR-Cas9 systems require a specific DNA sequence to latch on, limiting which genes could be edited. SPLICER uses newer Cas9 enzymes that do not need that sequence, opening up the door to new targets like the Alzheimer’s-related gene that the Illinois group focused on.

“Another problem we address in our work is precision in what gets skipped,” said graduate student Angelo Miskalis, a co-first author of the paper. “With current exon-skipping techniques, sometimes not all of the exon gets skipped, so there’s still part of the sequence we don’t want expressed. In the cookbook analogy, it’s like trying to skip a page, but the new page starts in the middle of a sentence, and now the recipe doesn’t make sense. We wanted to prevent that.”

There are two key sequence areas surrounding an exon that tell the cellular machinery which parts of a gene to use for making proteins: one at the beginning and one at the end. While most exon-skipping tools target only one sequence, SPLICER edits both the starting and ending sequences. As a result, the targeted exons are skipped over more efficiently, Miskalis said.

The Illinois group chose to target an Alzheimer’s gene for the first demonstration of SPLICER’s therapeutic abilities because while the target gene has been well-studied, efficient exon skipping has remained elusive in living organisms. The researchers targeted a specific exon coding for an amino acid sequence within a protein that gets cleaved to form amyloid-beta, which accumulates to form plaques on neurons in the brain as the disease progresses.

In cultured neurons, SPLICER reduced the formation of amyloid-beta efficiently. When analyzing the DNA and RNA output of mouse brains, the researchers found that the targeted exon was decreased by 25% in the SPLICER-treated mice, with no evidence of off-target effects.

“When we originally tried to target this exon with older techniques, it didn’t work,” said graduate student Shraddha Shirguppe, also a co-first author of the study. “Combining the newer base editors with dual splice editing skipped the exon at a much better rate than we were previously able to with any of the available methods. We were able to show that not only could it skip the whole exon better, it reduced the protein that produces the plaque in these cells.”

“Exon skipping only works if the resulting protein is still functional, so it can’t treat every disease with a genetic basis. That’s the overall limitation of the approach,” Perez-Pinera said. “But for diseases like Alzheimer’s, Parkinson’s, Huntington’s or Duchenne’s muscular dystrophy, this approach holds a lot of potential. The immediate next step is to look at the safety of removing the targeted exons in these diseases, and make sure we aren’t creating a new protein that is toxic or missing a key function. We would also need to do longer term animal studies and see if the disease progresses over time.”

At Illinois, Perez-Pinera also is affiliated with the department of Molecular and Integrative Physiology, the Carle Illinois College of Medicine, the Cancer Center at Illinois and the Carl R. Woese Institute for Genomic Biology. U. of I. Bioengineering professors Sergei Maslov and Thomas Gaj were coauthors of the paper. The National Institutes of Health, the Muscular Dystrophy Association, the American Heart Association, the Parkinson’s Disease Foundation and the Simons Foundation supported this work.

This work was supported by the National Institutes of Health grants 1U01NS122102, 1R01NS123556, 1R01GM141296, 1R01GM127497, T32EB019944 and 1R01GM131272.

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Largest magnetic anisotropy of a molecule measured at BESSY II

At the Berlin synchrotron radiation source BESSY II, the largest magnetic anisotropy of a single molecule ever measured experimentally has been determined. The larger this anisotropy is, the better a molecule is suited as a molecular nanomagnet. Such nanomagnets have a wide range of potential applications, for example, in energy-efficient data storage. Researchers from the Max Planck Institute for Kohlenforschung (MPI KOFO), the Joint Lab EPR4Energy of the Max Planck Institute for Chemical Energy Conversion (MPI CEC) and the Helmholtz-Zentrum Berlin were involved in the study.

The research involved a bismuth complex synthesized in the group of Josep Cornella (MPI KOFO). This molecule has unique magnetic properties that a team led by Frank Neese (MPI KOFO) recently predicted in theoretical studies. So far, however, all attempts to measure the magnetic properties of the bismuth complex and thus experimentally confirm the theoretical predictions have failed.

This important step has now been achieved by using THz electron paramagnetic resonance spectroscopy (THz-EPR) at the synchrotron radiation source BESSY II, which is operated by the HZB in Berlin.

“The results show in a fascinating way that our method can be used to determine extremely high values of the magnetic anisotropy with high accuracy. Through our cooperation with scientists from fundamental research, we are thereby making a great step forward in the understanding of this class of materials,” says Tarek Al Said (HZB), first author of the study, which was recently published in the Journal of the American Chemical Society.

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Propranolol reduces tremors in Parkinson’s disease

The standard medication levodopa does not always work against tremors in Parkinson’s disease, especially in stressful situations. Propranolol, however, does work during stress, providing insight into the role of the stress system in tremors. MRI scans reveal that propranolol directly inhibits activity in the brain circuit that controls tremors. Doctors may consider this medication when levodopa is ineffective.

People with Parkinson’s disease report that tremors worsen during stressful situations. ‘Tremors act as a sort of barometer for stress; you see this in all people with Parkinson’s’, says neurologist Rick Helmich from Radboud university medical center. The commonly used drug levodopa usually helps with tremors, but it tends to be less effective during stress, when tremors are often at their worst. Helmich and his team wanted to investigate whether a medication targeting the stress system could help and how this effect of stress on tremors works in the brain.

Mathematical calculations

The medication in question, propranolol, is a beta-blocker that inhibits the action of stress hormones. It was developed for high blood pressure and heart arrhythmias, has been around for a long time, and is already used as a standard treatment for essential tremor — a condition in which people experience tremors without other neurological symptoms. There were already indications that propranolol might reduce tremors in Parkinson’s, but until now, no thorough research has explored its potential effects.

Helmich and his team studied 27 people with Parkinson’s who experienced tremors. They were given propranolol on one day and a placebo on another day. A device on their hands measured the intensity of their tremors, while an MRI scan mapped brain activity. This was done both at rest and during a task involving stressful mathematical calculations. The stress response was measured by pupil size and heart rate, both of which increased during the calculations. As expected, without medication, tremors worsened during stress.

Amplifier

The study showed that propranolol reduced tremors both at rest and during stress. The MRI scans revealed how this works: after taking the medication, the brain circuit responsible for tremors showed less activity. Helmich explains: ‘We know that abnormalities in systems like the dopamine system cause tremors. Based on our study, we now think that the stress hormone noradrenaline acts as an amplifier, which increases tremor intensity in the brain’s movement area. Propranolol inhibits this amplifying effect and thus reduces symptoms.’

It surprised the researchers that propranolol also worked to reduce tremors at rest. ‘Apparently, our stress system is occasionally active, even at rest’, says researcher Anouk van der Heide. ‘This changes how alert someone is and leads to spontaneous fluctuations in tremors. We previously thought that the stress hormone system was only active under stress, but apparently, that’s too simplistic. It also plays a role at rest.’

Mindfulness

Helmich already prescribes propranolol for some Parkinson’s patients. ‘The most effective medication for Parkinson’s is levodopa. It not only helps with tremors but also with other symptoms, so that’s what we start with’, Helmich explains. ‘However, in about forty percent of patients, it is not effective against tremors. In that case, we first increase the dose, but if that doesn’t work, propranolol is an option. However, we must be cautious about side effects, such as low blood pressure.’

In addition to medication studies, Helmich’s team is also exploring lifestyle changes that could help with Parkinson’s. ‘It doesn’t take much to trigger a stress response, causing people to tremble more. Even something as simple as wondering: did I lock the front door? can set it off. We are currently investigating whether mindfulness can positively influence the stress system.’

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Paleobiologists unlock 500,000 years of fossil records: Climate change impacts and risks of marine carbon removal

A study co-led by Professor Moriaki YASUHARA and Ms Raine CHONG from the School of Biological Sciences, the Swire Institute of Marine Science, and the Institute for Climate and Carbon Neutrality at The University ofHong Kong (HKU), as well as Dr May HUANG from Department of Geosciences of Princeton University, has shed light on how the deep-sea ecosystem in the Southern Ocean has evolved over the past 500,000 years. The study, published in the journal Current Biology, reveals that temperature changes and food input have played distinct roles in shaping deep-sea ecosystems.

Deep-sea temperature is stable, with only minor changes occurring even over long-time scales. Despite this stability, deep-sea organisms are highly adapted to such stable environments, making them particularly sensitive to even slight temperature fluctuations. Unlike surface water, the deep sea lacks primary production due to the absence of sunlight, which prevents phytoplankton growth and photosynthesis. Instead, deep-sea organisms rely on food that descends from the ocean surface, known as particulate organic material or marine snow. This includes dead plankton, a primary food source of organisms living on the deep ocean floor.

A new study conducted by the research team, utilising empirical data from deep-sea fossils extracted from sediment cores spanning 500,000 years, clearly demonstrated that temperature and food input have significantly modified deep-sea communities over long time scales, each affecting different species.

Professor Yasuhara stated, ‘It’s important not only to advance fundamental science by understanding how ecosystems on our planet operate but also to address the growing challenges posed by human-induced climatic change.’

As global concern over ongoing human-induced climatic warming and its future escalation intensifies, scientists and engineers are working hard to develop mitigation technologies to combat climatic change. These geoengineering technologies, collectively referred to as ocean-based climate intervention (OBCI), include approaches such as marine carbon dioxide removal (mCDR), which aim to reduce future warming by putting and storing carbon or carbon dioxide in deep-sea sediment, where they remain stable due to the low-temperature and high-pressure environments.

One prominent example of mCDR is iron fertilisation, a process in which iron is added to the ocean surface to enhance primary production, resulting in increased sinking of organic carbon to the deep-sea floor. While mCDR and OBCI are technologically advanced and nearly ready for implementation, they have yet to be deployed on large scales. One major concern is how these technologies will affect deep-sea ecosystems.

Yasuhara continues, ‘Deep sea covers over 40% of our planet’s surface, and its ecosystem is known to be highly vulnerable. The deep sea also harbours countless species that are still undiscovered. I would say the vast majority of species remain unknown to us. Our study, using a fossil record from a deep-sea sediment core for the past 500,000 years, shows that both temperature and food input, driven by changes in natural iron fertilisation through dust input and the resulting surface production enhancement, have altered deep-sea ecosystems in different ways substantially. This means we must be cautious when making decisions about this important and delicate ecosystem. Careful ecosystem impact assessments are needed to evaluate, on a case-by-case basis, whether human-induced warming or mCDR involving surface productivity changes is more harmful. Only then can we make a cautious and sensible decision about whether to proceed with mCDR.’

Professor Yasuhara also remarked that the Southern Ocean can be seen as a ‘canary in a coal mine’ because it’s a key sensitive region in the global ocean circulation and climatic system. ‘Our study highlights the sensitivity of its deep-sea ecosystem. Increased deep-sea biological monitoring efforts in this region are needed, as it could provide early warning signals of climatic changes. Our study also showed that the present-day style of the deep-sea ecosystem in the Southern Ocean was established 430,000 years ago. I hope such a long-standing ecosystem won’t be completely altered in the near future, especially since we don’t know how much this human-induced warming will escalate and fundamentally change our global climatic system in future.’

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Public shows greater acceptance of RSV vaccine as vaccine hesitancy appears to have plateaued

A year after becoming available, vaccines to protect against RSV in newborns and older adults are being more widely accepted by the American public, according to a new Annenberg Public Policy Center (APPC) health survey conducted in November 2024.

Over half of U.S. adults (52%) think the vaccine given to pregnant individuals to protect their infants from RSV (respiratory syncytial virus) is effective, up from 42% in October 2023, soon after the Centers for Disease Control and Prevention (CDC) recommended the vaccine. And 61% say the RSV vaccine for adults age 60 and older is effective, up from 54% in October 2023.

The rise in perceived effectiveness for the RSV vaccine comes even though there has been no sign to date of a dreaded “tripledemic,” the wave of flu, Covid-19, and RSV illnesses that filled emergency rooms in the fall and winter of 2022-23 and may have resulted in over 100,000 U.S. deaths. As of Dec. 20, 2024, the CDC reports overall moderate levels of acute respiratory illness, though flu season is underway with levels increasing across the country, Covid-19 activity is increasing from low levels in some areas of the country, and RSV activity is high and increasing in most U.S. areas, especially in young children.

The rise also comes as several of president-elect Donald Trump’s nominees for leading policy-making health positions have cast doubt on the efficacy and safety of vaccines, notably Health and Human Services Secretary nominee Robert F. Kennedy Jr., who has said “no vaccine” is safe and effective, and CDC chief nominee Dave Weldon, who, like Kennedy, has promoted the disproven link between vaccines and autism.

The APPC survey findings are based on a nationally representative panel survey of 1,771 U.S. adults fielded from Nov. 14-24, 2024, and has a margin of error of ± 3.3 percentage points. For more on the survey, see the end of this news release or the topline.

Vaccine hesitancy may have plateaued

The past several years have shown evidence of increased vaccine hesitancy. However, by several measures in the November survey, including the RSV findings noted above, public acceptance of vaccination has risen slightly or held steady:

  • 86% of respondents say the measles, mumps, and rubella vaccine (MMR) is safe, up from 81% in October 2023. The rebound brings it back toward the 88% who perceived it as safe in August 2022.
  • 83% say the flu vaccine is safe, unchanged from October 2023.
  • 65% say the Covid-19 vaccine is safe, unchanged from last fall.
  • The perceived effectiveness of a variety of other vaccines is unchanged from October 2023.
  • Over three-quarters of the public would recommend various vaccines, when appropriate, to members of their families and households.

In addition, despite continuing attacks on the safety and efficacy of certain vaccines by some politicians, 9 in 10 respondents say it is important for parents to get their children vaccinated: 72% say it is very or extremely important and 19% say it is somewhat important. Only 10% say it is not at all or not very important that parents get their children vaccinated.

Flu vaccine vs. Covid-19

In the survey, U.S. adults view the seasonal flu shot as more effective at reducing the risk of getting a severe case of the flu this season (75%) than the Covid booster is at reducing the risk of getting a severe case of Covid this season (55%). There’s been a significant increase in understanding that the flu shot doesn’t necessarily prevent a person who is exposed to the flu from getting sick but it does make the infection less severe (54%, up from 48% in October 2023). Fewer people say they are unsure what effect a flu shot has on a person who is later exposed to someone with the flu (14%, down from 20%).

The November data show that fewer people have received or plan to receive the Covid booster, as compared with the flu shot:

  • Just over half of survey respondents (51%) either got the seasonal flu shot (40%) or say they are very likely to (11%) get it, compared with 38% who either got the latest Covid-19 booster (29%) or say they are very likely to (9%).
  • The most common reason people select to explain why they have received the Covid booster and the flu shot is to protect themselves against catching that illness (82% and 78%, respectively).
  • More people report getting the flu shot because they “get it every year” (76%) than those who report getting the Covid booster because they “get one every time a new booster comes out” (51%).
  • 68% know they can get a Covid booster and a flu shot in the same visit to a health care clinic or pharmacy, unchanged from October 2023, though there’s a significant increase in the number who report that this is definitely true (44%, up from 38% in October 2023).

Flu knowledge

  • Most people (80%) know the effectiveness of the seasonal flu shot varies year to year.
  • Although most people (69%) see this year’s flu vaccine as effective at reducing the risk of getting the flu (unchanged from October 2023), more people think it is ineffective this fall (20%) than last fall (15%).
    • In fact, early reports suggest that this seasonal flu vaccine may be less effective than last year’s: Based on reports from five South American countries, the CDC has said the effectiveness of the seasonal flu vaccine at cutting the risk of hospitalization among high-risk groups appears to be 35%, lower than the 51.9% seen in those countries last flu season, according to WebMD.
  • 69% know that there is value in getting a flu shot after November, but 19% are unsure.
  • Most people (80%) know it is possible to spread the flu to others even if you have no symptoms, up from 76% in January of 2023. (The CDC says that some “people can be infected with influenza viruses and have no symptoms but may still be able to spread the virus to their close contacts.”)
  • Most (71%) know that the flu shot is the best defense against seasonal flu.
  • However, only 42% believe that everyone 6 months of age and older should get a flu shot, unchanged from last year.

Beliefs in vaccine effectiveness and safety

Longstanding vaccines such as the MMR, polio, and Tdap (tetanus, diphtheria, and pertussis) vaccines are usually top-rated by the public in effectiveness, safety, and in recommendations that others get the vaccines. Newer vaccines such as the Covid-19 vaccine or those for which public health advice has recently changed — such as the CDC recommendation that adults 50 and older get a vaccine against pneumonia — are less familiar and often lower-rated by the public.

Recommending vaccines. Here are the public’s views on recommending vaccines to others:

  • MMR vaccine: 90% would be likely to recommend an MMR vaccine for a child in their household who is either between the ages of 12-15 months or 4 to 6 years old.
  • Polio vaccine: 88% would be likely to recommend a polio vaccine to a child in their household of 2 to 6 months old.
  • Tdap vaccine: 85% would be likely to recommend a Tdap vaccine to a child in their household of 11-12 years old or an adult in their family.
  • Shingles vaccine: 82% would be likely to recommend a shingles vaccine to someone age 50+ in their family.
  • HPV vaccine: 79% would be likely to recommend an HPV (human papillomavirus) vaccine for a child aged 11 or 12 years old in their household.
  • Pneumonia vaccine: 77% would be likely to recommend a pneumonia vaccine to a person aged 50 or older in their family, down from 84% who were likely to recommend it to someone 65 or older in their family in April 2022. The CDC recommended lowering the age for the vaccine on Oct. 23, 2024, weeks before this survey was fielded.

Vaccine safety. Public views on vaccine safety:

  • MMR: 86% say the MMR vaccine is safe, up from 81% in October 2023 (as noted above)
  • Flu: 83% say the flu vaccine is safe, unchanged
  • Covid-19: 65% say the Covid-19 vaccine is safe, unchanged from October 2023 but lower than 73% in August 2022.

Vaccine effectiveness. Public views on vaccine effectiveness are stable with the exception of RSV, which rose as noted above. The following percentages saw these vaccines as effective. Comparisons are to October 2023, if this question was asked then:

  • MMR: 86% see the vaccine as effective (unchanged)
  • Polio: 85%
  • Tdap: 80%
  • Flu: 75% (unchanged)
  • Shingles: 74% (unchanged)
  • Pneumonia: 71% (unchanged)
  • HPV: 65% (unchanged)
  • Covid-19: 65% (unchanged)
  • RSV for adults 60 and older: 61%, up from 54% in October 2023
  • RSV for pregnant individuals: 52%, up from 42% in October 2023

APPC’s Annenberg Science and Public Health knowledge survey

The survey data come from the 22nd wave of a nationally representative panel of 1,771 U.S. adults conducted for the Annenberg Public Policy Center by SSRS, an independent market research company. Most have been empaneled since April 2021. To account for attrition, small replenishment samples have been added over time using a random probability sampling design. The most recent replenishment, in September 2024, added 360 respondents to the sample. This wave of the Annenberg Science and Public Health Knowledge (ASAPH) survey was fielded Nov. 14-24, 2024. The margin of sampling error (MOE) is ± 3.3 percentage points at the 95% confidence level. All figures are rounded to the nearest whole number and may not add to 100%. Combined subcategories may not add to totals in the topline and text due to rounding.

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Foundational technology to make cancer cells revert to normal cells?

Despite the development of numerous cancer treatment technologies, the common goal of current cancer therapies is to eliminate cancer cells. This approach, however, faces fundamental limitations, including cancer cells developing resistance and returning, as well as severe side effects from the destruction of healthy cells.

KAIST (represented by President Kwang Hyung Lee) announced on the 20th of December that a research team led by Professor Kwang-Hyun Cho from the Department of Bio and Brain Engineering has developed a groundbreaking technology that can treat colon cancer by converting cancer cells into a state resembling normal colon cells without killing them, thus avoiding side effects.

The research team focused on the observation that during the oncogenesis process, normal cells regress along their differentiation trajectory. Building on this insight, they developed a technology to create a digital twin of the gene network associated with the differentiation trajectory of normal cells.

Through simulation analysis, the team systematically identified master molecular switches that induce normal cell differentiation. When these switches were applied to colon cancer cells, the cancer cells reverted to a normal-like state, a result confirmed through molecular and cellular experiments as well as animal studies.

This research demonstrates that cancer cell reversion can be systematically achieved by analyzing and utilizing the digital twin of the cancer cell gene network, rather than relying on serendipitous discoveries. The findings hold significant promise for developing reversible cancer therapies that can be applied to various types of cancer.

Professor Kwang-Hyun Cho remarked, “The fact that cancer cells can be converted back to normal cells is an astonishing phenomenon. This study proves that such reversion can be systematically induced.”

He further emphasized, “This research introduces the novel concept of reversible cancer therapy by reverting cancer cells to normal cells. It also develops foundational technology for identifying targets for cancer reversion through the systematic analysis of normal cell differentiation trajectories.”

The study was supported by the Ministry of Science and ICT and the National Research Foundation of Korea through the Mid-Career Researcher Program and Basic Research Laboratory Program. The research findings have been transferred to BioRevert Inc., where they will be used for the development of practical cancer reversion therapies.

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Crossing the Uncanny Valley: Breakthrough in technology for lifelike facial expressions in androids

A research group led by Osaka University has developed a technology that allows androids to dynamically express their mood states, such as “excited” or “sleepy,” by synthesizing facial movements as superimposed decaying waves.

Even if an android’s appearance is so realistic that it could be mistaken for a human in a photograph, watching it move in person can feel a bit unsettling. It can smile, frown, or display other various, familiar expressions, but finding a consistent emotional state behind those expressions can be difficult, leaving you unsure of what it is truly feeling and creating a sense of unease.

Until now, when allowing robots that can move many parts of their face, like androids, to display facial expressions for extended periods, a ‘patchwork method’ has been used. This method involves preparing multiple pre-arranged action scenarios to ensure that unnatural facial movements are excluded while switching between these scenarios as needed.

However, this poses practical challenges, such as preparing complex action scenarios beforehand, minimizing noticeable unnatural movements during transitions, and fine-tuning movements to subtly control the expressions conveyed.

In this study, lead author Hisashi Ishihara and his research group developed a dynamic facial expression synthesis technology using “waveform movements,” which represents various gestures that constitute facial movements, such as “breathing,” “blinking,” and “yawning,” as individual waves. These waves are propagated to the related facial areas and are overlaid to generate complex facial movements in real time. This method eliminates the need for the preparation of complex and diverse action data while also avoiding noticeable movement transitions.

Furthermore, by introducing “waveform modulation,” which adjusts the individual waveforms based on the robot’s internal state, changes in internal conditions, such as mood, can be instantly reflected as variations in facial movements.

“Advancing this research in dynamic facial expression synthesis will enable robots capable of complex facial movements to exhibit more lively expressions and convey mood changes that respond to their surrounding circumstances, including interactions with humans,” says senior author Koichi Osuka. “This could greatly enrich emotional communication between humans and robots.”

Ishihara adds, “Rather than creating superficial movements, further development of a system in which internal emotions are reflected in every detail of an android’s actions could lead to the creation of androids perceived as having a heart.”

By realizing the function to adaptively adjust and express emotions, this technology is expected to significantly enhance the value of communication robots, allowing them to exchange information with humans in a more natural, humanlike manner.

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Individual leopards can be identified by their roars

Each leopard has its own unique roar through which it can be identified, a new study finds.

In the first large-scale paired camera trap and autonomous recording survey for large African carnivores, researchers were able to identify individual leopards by their vocalisations with 93% accuracy.

It has been hailed as an important first step towards using bioacoustics in the conservation of leopards.

Leopards are listed as ‘vulnerable’ to extinction according to the IUCN Red List of Threatened Species mainly due to habitat loss and human-wildlife conflict.

But because leopards are solitary, nocturnal creatures that live across huge expanses of terrain, scientists struggle to gather reliable data that would help them reverse population declines.

There is little scientific research about the ‘sawing roar’ of a leopard — a repeated low-frequency pattern of strokes, often audible from at least a kilometre away, used primarily to attract mates and for territorial defence.

But studying leopards through the sounds they make — a technique known as bioacoustics and more typically used to monitor birds and marine species — would have the advantage of allowing researchers to monitor much larger areas.

It could lead to more complex studies such as population estimates, a key metric for helping policymakers and conservation practitioners understand how to manage landscapes and mitigate human-wildlife conflicts.

The research team conducted their study across a 450km2 expanse of the Nyerere National Park in Tanzania, where they attached 50 pairs of cameras to trees along roads and trails.

They placed microphones next to each camera so that they could identify the leopard from the camera and then extract the roaring bouts from the audio.

They then used a modelling system to analyse the temporal pattern of a leopard’s roar, and found individual identification was possible, with an overall accuracy of 93.1%.

The study shows that using multiple forms of technology to record complementary data can exploit a wider variety of species traits than single technology studies alone.

Lead author Jonathan Growcott, a PhD student at the University of Exeter, said: “Discovering that leopards have unique roars is an important but fundamentally quite basic finding that shows how little we know about leopards, and large carnivores in general.

“We hope it will allow leopards to become the focus of more acoustically complex science such as population density studies and open the door to more work on how large carnivores use vocalisations as a tool.

“Importantly, our success in using a combination of different types of technology could hopefully lead others to think about how to integrate different types of technology into their research, as the rich data this provides could really push science ahead and help us understand ecosystems and landscapes in a much more holistic way.”

The research was a collaborative effort between the University of Exeter, the Wildlife Conservation Unit at the University of Oxford, Lion Landscapes, Frankfurt Zoological Society, TAWIRI (Tanzania Wildlife Institute for Research) and TANAPA (Tanzania National Parks Authority), as well as computer scientists from Exeter and Oxford.

It was presented by Growcott at the British Ecological Society Annual meeting in Liverpool earlier this month, an event which brought together 1,500 ecologists.

Hazel Norman, CEO of the British Ecological Society said: “This study showing that individual leopards can be identified and monitored just through their roars is a brilliant example of how ecologists are applying novel ideas and technologies to uncover fascinating new insights into our natural world.

“Jonathan presented this research at our recent British Ecological Society Annual Meeting in Liverpool, which is a brilliant forum for ecologists to share their research and ideas with the ecological community and beyond.”

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