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Every time I interview someone from an AI scribe company, I ask if it’s OK to record the interview for my notes and make a joke about the ironic situation.

Turns out, not everyone is asking, and people have started to record their daily conversations, such as first dates, without asking. “This Conversation is Being Recorded. They All Are” is the Wall Street Journal’s headline. What a hellscape.

Continue to STAT+ to read the full story…

Multilingual Voice AI for Postoperative Cataract Follow-Up in Turkish Speaking Patients in the United Kingdom: Patient and Public Involvement Focus Group Study

Background: Conversational voice AI assistants can automate postoperative follow-up calls in high-volume, low-complexity pathways such as cataract surgery but may widen health inequalities if language access and inclusive design are not built in. This patient and public involvement focus group was conducted to inform the Turkish-language adaptation of Dora ahead of a forthcoming multilingual clinical trial at Moorfields Eye Hospital. Objective: This study aims to inform the Turkish-language adaptation of Dora by gathering input from Turkish speaking community contributors about their experiences with UK ophthalmic care, language-related barriers, and design requirements for an equitable voice AI. Methods: We conducted a 1-time, 2-hour patient and public involvement focus group with 7 Turkish speaking adults recruited via the Derman community charity. The session ran in 2 phases: contributors first discussed their experiences with UK ophthalmic care, then evaluated a prerecorded Turkish-language telephone call from a voice AI to a Turkish speaking volunteer. The session was delivered bilingually, recorded with consent, and synthesized using an approach informed by the principles of reflexive thematic analysis. The voice AI uses automatic speech recognition and neural text-to-speech, with a large language model–based dialog manager for open-ended conversation within a postoperative review protocol. Results: Contributors described how pathway delays and limited language support shape their care, including reliance on family members for translation and concerns about privacy and autonomy. A language-concordant voice AI was conditionally acceptable for standardized postoperative follow-up, provided specific safeguards were met. Priorities included advance notice of calls, caller verification, privacy assurances, a clear standard Turkish accent at a slower pace, tolerance for regional dialects, interpersonal warmth, interactivity, accessibility for low vision and low literacy, and clinician escalation for complex issues. These priorities were synthesized into a 10-point checklist: preparation, verification, confidentiality, clarity and pace, voice, empathy, interactivity, dialect handling, accessibility, and efficiency. Conclusions: For patients facing language barriers, conversational voice AI may complement existing services when implemented with clear verification, privacy protections, and a defined scope under clinician oversight. The 10-item checklist will guide the Turkish-language adaptation of Dora and will be tested alongside similar consultations with other language communities in the forthcoming multilingual cataract follow-up trial.
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New study supports testing of Merck’s Ebola vaccine in DRC outbreak

New data from a study in humans provides additional support to the idea that Merck’s Ebola vaccine Ervebo, licensed to target the Zaire species of ebolaviruses, could also offer some protection against another species currently circulating in a rapidly expanding outbreak in the Democratic Republic of the Congo.

The new paper, published Wednesday in the New England Journal of Medicine after previously having been posted online before peer review, is one of a growing number of studies pointing to the possibility that the vaccine could be used to target the Bundibugyo species of ebolaviruses. 

Read the rest…

New Target on Tumor Blood Vessels Could Expand Immunotherapy Responses

Immune checkpoint inhibitors have transformed cancer treatment, producing long-lasting—and sometimes curative—responses in patients with advanced malignancies. Yet only a minority of patients benefit, particularly those whose tumors have spread to the liver, where immunotherapy often proves less effective.

A new preclinical study from researchers at the German Cancer Research Center in Heidelberg suggests the answer may lie not within the cancer cells themselves, but in a specialized population of cells lining the tumor’s blood vessels. The findings, published in Cancer Research, identify lipoprotein lipase (LPL)-expressing tumor endothelial cells as critical regulators of T-cell infiltration into liver metastases and point to a new strategy for enhancing immunotherapy in tumors that are otherwise resistant to treatment.

The discovery builds on growing evidence that remodeling tumor blood vessels can improve immunotherapy. Anti-angiogenic agents such as bevacizumab, which targets the VEGF pathway, have already demonstrated clinical benefit when combined with immune checkpoint blockade. In the landmark IMbrave150 trial, atezolizumab plus bevacizumab significantly improved overall survival compared with sorafenib in patients with advanced hepatocellular carcinoma.

Despite that success, durable responses remain relatively uncommon. Approximately 30% of patients experienced an objective response to the combination therapy, while only about eight percent achieved a complete response. Those results suggest that targeting VEGF alone does not fully overcome the barriers preventing immune cells from reaching and attacking tumors.

To better understand those barriers, the investigators analyzed how blood vessel cells within and surrounding liver metastases responded over time after T-cell therapy. Their analyses uncovered a previously unrecognized subgroup of tumor endothelial cells that express LPL, an enzyme best known for its role in fat metabolism but not previously linked to antitumor immunity.

Rather than serving as passive conduits for blood flow, these endothelial cells actively orchestrated the immune response.

The researchers found that LPL-positive endothelial cells helped activated CD8-positive T cells leave the bloodstream and enter metastatic tumors. Once there, the T cells were able to recognize and destroy cancer cells, leading to regression of liver metastases in mouse models.

The study also revealed why these specialized blood vessel cells appear to be so important. Many cancers evade immune attack by reducing expression of major histocompatibility complex class I (MHC-I), the molecular display system that allows T cells to recognize tumor-derived proteins. Without adequate antigen presentation, even activated T cells struggle to identify malignant cells.

The authors found that LPL-positive endothelial cells compensate for this weakness. Instead of relying solely on tumor cells to present antigens, the endothelial cells themselves captured tumor proteins and displayed them through MHC-I, effectively providing T cells with the information needed to locate nearby cancer cells.

As the authors write, “LPL enhanced MHC-I-dependent cross-presentation of tumor antigens on tumor endothelial cells, thereby promoting T-cell infiltration.”

That interaction created a positive feedback loop. Once activated T cells recognized antigens displayed by the endothelial cells, they also targeted those blood vessel cells, further amplifying immune activity within the tumor microenvironment.

Genetic experiments reinforced the importance of the pathway. Increasing LPL expression specifically in endothelial cells enhanced T-cell infiltration into liver metastases, while eliminating LPL from those cells impaired immune cell recruitment and reduced the effectiveness of T-cell–mediated tumor control.

Importantly, the findings extended beyond animal models.

When the investigators examined human liver metastasis samples, they observed that tumors containing higher numbers of LPL-positive blood vessels also contained significantly more infiltrating T cells, suggesting that the mechanism may operate in patients as well.

The authors conclude that “LPL-positive tumor endothelial cells orchestrate activated CD8-positive T-cell homing into immunologically cold tumors with low baseline MHC-I expression.”

The work also helps explain why vascular-targeted therapies benefit only a subset of patients receiving immunotherapy. Previous research has largely focused on normalizing abnormal tumor blood vessels or increasing expression of molecules that help immune cells adhere to vessel walls. While those approaches improve immune cell access, they do not address another fundamental obstacle: many tumors simply fail to present enough antigens for T cells to recognize.

By acting as surrogate antigen-presenting cells, LPL-positive endothelial cells appear capable of overcoming that limitation, enabling T cells to infiltrate tumors that would otherwise remain immunologically “cold.”

The findings suggest that future combination strategies may need to extend beyond VEGF inhibition and instead directly promote the immune-supporting functions of tumor blood vessels.

Although additional studies will be needed to determine whether therapies can safely increase LPL activity in patients, the work identifies the protein as both a potential biomarker and a therapeutic target. Measuring LPL-positive blood vessels could help identify patients most likely to benefit from immunotherapy combinations, while therapies that enhance this endothelial cell program could potentially expand responses among patients whose tumors currently resist immune attack.

As the authors conclude, enhancing antigen presentation by tumor endothelial cells “presents a promising approach to compensate the intrinsic inability of tumor cells and boost antitumor immunotherapy,” offering a potential new avenue for turning immunologically cold liver metastases into tumors that respond to immune-based treatment.

The post New Target on Tumor Blood Vessels Could Expand Immunotherapy Responses appeared first on Inside Precision Medicine.

Cancer’s Hidden Axis: Genetic Background Drives Tumor Evolution

Imagine reversing that very first oncogenic mutation. Now press play. Will it always grow the same tumor?

Cancer genetics has assumed yes—or close enough—for decades. After sequencing millions of tumors, researchers found that KRAS, BRAF, EGFR, and HRAS repeatedly rear their heads. Precision oncology matches tumors to targeted therapies based on the idea that driver mutations determine their fate.

However, cancer rarely repeats itself. Two patients with the same driver mutation can have very different diseases. Their tumors develop differently, progress faster, and respond differently to identical treatments. “We all have different inherited genes, and we all live different lives. We’re exposed to different things,” Sarah J. Aitken, PhD, first author of the study and an assistant professor of pathology and a member of the Center of Molecular and Cellular Oncology at Yale Cancer Center, told Inside Precision Medicine. “That becomes very complicated to disentangle—what’s causing what and why different patients might respond to different things in different ways even though they seem to have the same disease.”

Researchers have blamed environmental exposures, additional mutations, and simple bad luck. But a study published in Nature  argues that another determinant has been hiding in plain sight all along: the inherited genome in which those mutations arise. Rather than acting independently, cancer-driving mutations may interact extensively with an individual’s genetic background, fundamentally altering how tumors evolve from their earliest beginnings. The implications go beyond mouse genetics. The same mutation—which clinicians may use to guide treatment—may have different biological effects in different people. Instead, its effects depend on the surrounding inherited genetic landscape.

“One of the goals in diagnostics and precision medicine is to identify the genetic change, driver mutation, or specific marker in this particular cancer that will work and cure the patients—it does in some people, but not in many others,” said Aitken. “Even if what we’re trying to do is identify this magic target to treat, if the combination of genetic backgrounds is going to make someone’s driver behave differently in different people, it doesn’t tell us what we do need to do, but it maybe tells us why different people respond in different ways. So… maybe we need to be looking at this particular driver in this genetic background, not just the specific driver itself.”

Earliest cancer moments, rewound

Most cancer research begins at the end of the story. Before being diagnosed, a tumor has evolved for years or decades. Sequencing data can help scientists reconstruct that history, but they cannot directly observe how the first mutated cells competed, survived, or disappeared. Human studies are complicated because each patient has unique genetics, environmental exposures, lifestyle, diet, and chance.

Aitken and colleagues wanted to eliminate most of those variables. So, they did something humans cannot do to untangle those variables: they repeated cancer evolution hundreds of times.

In a classic chemically induced liver cancer model, they gave four genetically distinct mouse strains a single dose of the DNA-damaging carcinogen diethylnitrosamine (DEN) at the same developmental stage. All mice were exposed under the same lab conditions. The tumors were analyzed using whole-genome sequencing, transcriptomics, and histopathology.

The design allowed one variable to dominate: inherited genetics. “The idea was that we could remove a lot of that heterogeneity that exists in human populations,” Aitken explained. “We can remove all the different variables except inherited genetics, so we know exactly what we’ve exposed them to. We give them one dose of a single drug at the same time. Everything else is the same. Then, any differences we see, we think we can ascribe to those inherited differences.”

The design resembles evolutionary biologist Stephen Jay Gould’s famous thought experiment from his 1989 book Wonderful Life of “replaying the tape of life,” asking whether evolution would unfold the same way if history could begin again. Here, instead of replaying the evolution of life, the researchers replayed the evolution of cancer hundreds of times under nearly identical conditions.

Identical mutations, different biology

The researchers started with simple expectations. One genetic background may have produced tumors faster than another due to more mutations. However, the data indicated otherwise. “We had preconceptions,” Martin S. Taylor, PhD, co-senior author from the Medical Research Council Human Genetics Unit at the University of Edinburgh, told Inside Precision Medicine. “They proved to be wrong, as is often the case. But you do the experiment.”

The researchers found that the most cancer-prone mouse strain often needed fewer genetic changes to become cancerous. More resistant strains mutated but developed tumors slower. This changed the study’s focus from mutagenesis to evolution. “It wasn’t that mutation load was driving things,” Taylor said. “It was differences in selection.”

It seems subtle, but it changes how researchers view early tumor development. Mutations are constant, and most disappear without consequence. Mutated cells that survive, grow, and become cancerous are selected. Even more surprising, identical driver mutations rewired downstream biology differently depending on the inherited genome.

Aitken pointed to the tumor suppressor p53 as an example. “In some of the strains, when you mutate one particular driver, it makes p53 signaling go up. In other strains, exactly the same driver—exactly the same thing that we’re trying to diagnose—makes p53 go in the opposite direction.”

That observation is striking because driver mutations were once considered discrete molecular events with predictable downstream effects. In this case, the inherited genome changed how mutations spread through signaling networks.

The study found significant interactions between p53 signaling, TGFβ, and PPAR pathways, which regulate cell growth, differentiation, metabolism, inflammation, and programmed cell death. Most importantly, all strains activated the core MAPK pathway. The broader cellular response to activation changed.

When they studied early tumor formation, researchers found another surprise. Conventional thinking holds that cancer develops gradually through mutations until a cell becomes malignant. However, using lesion segregation, which Taylor’s group discovered several years earlier, the researchers were able to reconstruct the first generations of cells after DNA damage.

Several tumors appeared immediately. Others took several rounds of cellular evolution to clone. The most susceptible mouse strain, C3H, often transformed after one major driver mutation. More resistant strains had two or more driver events before tumors formed. Many early cellular lineages disappeared before contributing to cancer, even with similar mutations.

Those findings suggest a major perspective shift. Researchers may need to ask why certain inherited genomes help mutated cells survive the early rounds of evolutionary competition rather than why some people have more mutations. “We were initially expecting that perhaps we’d see more mutations in the mice that developed tumors more quickly,” Taylor said. “Actually, we saw sort of the opposite.” Selection, not mutation, emerged as the dominant force.

Ordinary genetic variation, extraordinary effects

A part of the study that surprised the researchers was that the study mice were not engineered to carry high-risk cancer mutations. They were not inherited cancer models. Instead, they represented natural genetic diversity.

“These are basically wild-type mice,” Taylor said. “They haven’t got strong predisposition effects. They’ve naturally accumulated variation, which is probably more reflective of what’s happening in the human population than genetically modified mouse models.” That observation broadens the significance of the findings.

Most inherited cancer research has focused on rare, high-penetrance mutations like BRCA1, BRCA2, or TP53 that greatly increase cancer risk. Mutations account for a small percentage of cancers. Most are caused by thousands or millions of relatively common variants that have little effect on disease risk. This Nature study suggests that ordinary differences may collectively influence tumor evolution more than previously thought.

Aitken and Taylor avoid exaggerating. The controlled chemically induced liver cancer model was used in mice only. Human cancers develop over decades due to environmental exposures, aging, inflammation, and other biological factors.

Thus, this study’s driver mutations cannot predict human cancers. The work’s significance is its principle. Eliminating nearly every confounding variable except inherited genetics showed that germline variation can influence nearly every stage of tumor evolution, from the number of mutations needed for transformation to which oncogenic drivers succeed, how they interact with cellular signaling pathways, and how quickly cancers emerge.

Human population observations support the findings. Previous genomic studies have found differences in driver mutation frequency among ancestry groups that are difficult to explain by environmental exposure or mutational processes.

Taylor believes the study offers one plausible biological mechanism. “We know that you get differences in driver frequencies across different population groups,” he said. “We don’t really have a very good handle on why that’s the case.” The interactions observed between inherited genetic background and driver mutations, he argues, may represent part of that explanation.

Putting the precision in “precision oncology”

The implications of this paper could be paradigm shifting for precision oncology, which has transformed cancer care by reading the genomes of tumors. This study suggests the next frontier may involve reading two genomes simultaneously. One belongs to the cancer. The other belonged to the patient long before the first cancer cell appeared. Together, they may determine far more than researchers once imagined.

But there’s still a long way to go in this tale before we can change people’s lives for the better. “It doesn’t tell us what we need to do,” Aitken said. “But maybe it tells us why different people respond in different ways. Maybe we need to be looking at this particular driver in this genetic background—not just the specific driver itself.”

Cancer is often described as evolution unfolding inside the body. But evolution never begins with a blank slate. Every driver mutation emerges within an inherited genome shaped over millions of years of evolutionary history—a genome that may influence which mutations survive, which biological pathways they perturb, and ultimately whether a damaged cell ever becomes a tumor. The mutation may ignite the process. This study suggests the inherited genome helps decide how the fire spreads.

The post Cancer’s Hidden Axis: Genetic Background Drives Tumor Evolution appeared first on Inside Precision Medicine.

Therapy‑Driven DNA Changes in Pediatric Tumors Can Spur Resistance

Research led by the Hospital for Sick Children in Toronto shows chemotherapy and radiotherapy are key sources of mutations in relapsed childhood tumors and that different treatments leave distinct mutational signatures.

As described in Nature, across all mutations in these pediatric tumors, about 15% can be clearly traced to four chemotherapies, and most of that therapy‑linked damage comes from platinum drugs like cisplatin, carboplatin, and oxaliplatin.

After platinum chemotherapy, temozolomide, 5‑FU, and thiopurines were the next‑most clearly mutation‑linked drugs in this study, but each added only a small fraction of the total mutational burden compared with platinum drugs.

“Many of the drugs used to treat children with cancer cause unfortunate long term side effects, including heart issues and secondary cancers,” lead author Adam Shlien, PhD, told Inside Precision Medicine.

“These drugs can also lead to somatic mutations, although the total genomic burden of this wasn’t known. Whether these mutations are associated with drug resistance in childhood cancer was also mostly unknown.”

In this study, the researchers assembled a multi‑national precision‑oncology cohort of 611 tumors from 544 children and young adults enrolled in three whole genome sequencing‑based programs, focusing on aggressive, relapsed or metastatic cancer.

The team then looked at exposure to 86 types of therapy in 13 drug classes, as well as radiotherapy, and created a detailed record of cycle dates, doses, and routes of administration for each child. They also recorded the number of drugs or other treatments the cancer patients were exposed to, looked for mutation patterns in tumor DNA linked to specific chemotherapy agents and tracked when these first appeared after treatment.

“It was striking how many mutations are associated with therapy—when the tumor cells survive, they frequently acquire thousands of mutations and many of these are tightly linked to the type of therapy that was used,” explains Shlien.

Platinum drugs were the biggest contributors to tumor mutation signatures. They caused a large fraction of all therapy‑related mutations and left clear, characteristic mutation patterns that appeared in a short amount of time after starting treatment, sometimes in as little as three months.

Although the presence of mutations did not necessarily lead to drug resistance or relapse, tumors with strong platinum‑linked patterns often showed activation of genes known to help cancer cells resist treatment with platinum drugs.

This finding was confirmed in the pediatric study cohort and in adults with cancer treated with platinum chemotherapy. Patients whose tumors carried these patterns had worse outcomes when treated with platinum drugs.

This study opens the door to using these mutation patterns to guide care. This could include deciding when to avoid re‑using a drug, or when to consider lowering doses of mutagenic treatments like platinum chemotherapies in settings where cure rates are already high. It also shows that these treatment‑induced mutation patterns are not just signs of past therapy but can be an early warning of the emergence of drug‑resistant cancer cells.

“Now that we have comprehensively defined which therapy-associated mutation patterns are acquired in childhood cancer, and when they emerge, we can start to think about screening patients for these signatures for the early detection of drug-resistant clones,” says Shlien.

The post Therapy‑Driven DNA Changes in Pediatric Tumors Can Spur Resistance appeared first on Inside Precision Medicine.

Transmissible Cancer Discovered in Freshwater Fish

Researchers headed by a team at the University of Vermont have discovered that mysterious black skin lesions afflicting catfish in Lake Memphremagog and other New England and Canadian lakes are caused by a transmissible form of cancer, the first ever identified in a freshwater fish species. The scientists’ studies showed that the cancer cells behave more like parasites than conventional tumors, moving from fish to fish.

The discovery marks only the fourth type of transmissible cancer identified in the animal kingdom, and the first in any fish or freshwater species. Previous ones include the Tasmanian devil’s facial tumor disease, a transmissible venereal tumor in dogs, and transmissible leukemia-like diseases in clams, mussels, and other bivalve mollusks. The researchers do emphasize that the disease poses no known risk to humans. The cancer cells cannot infect or survive in another species, and the fish are safe to handle and study.

The new discovery sheds light on how cancer can spread in the wild, and raises important questions about where this cancer originated, how it will affect fish health and populations, and also how cancer works in all animals including humans.

Julie Dragon, PhD, a researcher at the UVM Cancer Center in the Larner College of Medicine, suggests that understanding this newly discovered transmissible cancer could offer new insights into cancer biology more broadly. “By studying how cancers survive and spread outside their original host, we can learn a great deal about what keeps cancers contained—and what happens when those boundaries break down,” she said. “These fish provide an opportunity to look at evolution of cancer.”

Dragon is co-lead author of the researchers’ published report in Nature, titled “Brown bullhead catfish melanoma represents a novel transmissible cancer,” in which they stated, “We found extensive genomic evidence to suggest these melanistic lesions represent a transmissible cancer, to our knowledge, the first known occurrence in a fish species and the first found in a freshwater aquatic setting.”

Since 2012, anglers and biologists have reported a striking increase in brown bullhead catfish (Ameiurus nebulosus) with raised black skin patches in the cross-border lake shared by Vermont and Quebec. By 2014, nearly one in three fish showed the dark lesions. Because brown bullhead are considered indicators of environmental quality, the researchers suspected a contaminant or pathogen linked to pollution. “At first, we thought this disease might be a virus, but that wasn’t panning out,” said Dragon.

Instead, scientists found that these lesions turned out to be melanoma, a skin cancer. “This was surprising,” Dragon said, “and we wanted to know how a bottom-dwelling fish was getting a cancer we associate with exposure to too much sunlight.” For their reported study Dragon and colleagues took what she describes as a “deep dive,” into the genetics of the cancer cells.

UVM professor and cancer researcher Julie Dragon co-leads dissection and tissue collection of catfish with melanoma skin cancer at the Gateway Center on the shore of Lake Memphremagog, Newport, Vermont. Additional participants: Elizabeth Murchison, professor at the University of Cambridge, UK; her post-doctoral associate Zoe Clarke; USGS post-doctoral research fish health biologist Cheyenne Smith; her undergraduate student intern Sam Williams (not shown in these photos); Peter Emerson, fish biologist with the Vermont Department of Fish & Wildlife. The team sampled tissue from 17 fish.
UVM professor and cancer researcher Julie Dragon co-leads dissection and tissue collection of catfish with melanoma skin cancer at the Gateway Center on the shore of Lake Memphremagog, Newport, Vermont. Additional participants: Elizabeth Murchison, professor at the University of Cambridge, U.K.; her post-doctoral associate Zoe Clarke; USGS post-doctoral research fish health biologist Cheyenne Smith; her undergraduate student intern Sam Williams (not shown in these photos); Peter Emerson, fish biologist with the Vermont Department of Fish & Wildlife. The team sampled tissue from 17 fish. [University of Vermont]

Using whole-genome sequencing, the team compared DNA from tumors and healthy tissues in affected fish. They expected to find a genetic mutation that makes the fish susceptible to having their own cells become cancerous. Instead, they found that the cancer cells were much more closely related to each other than to their host fish—the signature of a clonally transmissible cancer, in which tumor cells themselves act as infectious agents.

“Hundreds of thousands of genetic variants are shared among tumor samples but absent from host fish, vastly exceeding levels seen in conventional cancers,” the authors reported in their paper.

The research team is now working to understand how the cancer cells spread between animals. “It seems to only happen in larger fish that are of spawning age,” said study co-lead Mark Henderson, PhD, fish biologist at UVM’s Rubenstein School of Environment and Natural Resources. “Maybe some part of spawning behavior leads to the spreading of the cancer between animals.”

The study notes that pollutants or hormonal changes could weaken immune systems, making the lake’s brown bullhead fish more vulnerable to infection. Naturally occurring arsenic may also play a role. The team did find that the fish cancer cells have elevated levels of arsenic and the geographic distribution of the cancer appears to have correlation with levels of arsenic in the lakes’ surrounding soil. “Arsenic is found naturally throughout New England, and there’s really high concentrations of it in the Vermont’s Northeast Kingdom as well as up through Maine, which is where we’ve also seen evidence of this cancer,” said Henderson.

The cancer’s ecological impact remains uncertain. Some transmissible cancers are devastating—the Tasmanian devil tumor has wiped out 90% of some populations. In contrast, the dog tumor has coexisted with its hosts and has done for thousands of years. In Lake Memphremagog, heavily diseased bullhead can survive for years, but long-term population effects are still unknown.

The researchers are beginning to explore how long this cancer may have been around, and how common transmissible cancers may be. They are exploring ponds and rivers in Massachusetts to learn more about the distribution of the cancer and to see if it may have originated there. “Our contention is that maybe it’s not as rare as everyone thinks. We’re just not seeing it,” said Dragon. “In the case of transmissible cancers, it may be that we don’t see many simply because we aren’t looking for them.”

In their paper the team concluded, “Although we cannot rule out a role for conventional pathogens in the original emergence or ecological transmission of this disease, the genomic evidence presented here overwhelmingly supports a transmissible cancer in which the tumor cells themselves act as the infectious entity.”

The post Transmissible Cancer Discovered in Freshwater Fish appeared first on GEN – Genetic Engineering and Biotechnology News.

Breath Sensor Monitors Fat Metabolism at Home

Scientists in Switzerland have developed a portable breath detector that can accurately measure acetone released into the breath when the body burns fat. The smartphone-assisted device allows patients to monitor their metabolism at home and could help doctors personalize treatment for metabolic diseases such as obesity and diabetes.

Acetone levels in the breath have long been recognized as an indicator of metabolic activity, since its concentration rises when the body shifts from using carbohydrates to fats as the primary energy source. However, accurate measurements have traditionally required bulky and expensive laboratory equipment, while consumer devices have lacked the sensitivity needed to reliably measure acetone, especially at lower concentrations. 

“If we want to make that information available to patients, we need to shrink those technologies into compact, user-friendly devices,” said Andreas Güntner, PhD, assistant professor at ETH Zurich and senior author of the study published today in the Device journal.

To make a compact breath analyzer, Güntner’s team used a chemoresistive sensor that changes its electrical properties in the presence of acetone. These types of sensors are known for their high sensitivity, rapid response, low power consumption, and small size. During each measurement, the accompanying smartphone app coaches users to exhale with the right force and duration, while quality controls can reject improper breaths or contaminated air. This design makes the sensor easy to use while ensuring accurate measurements. 

The breath detector was used to analyze 312 breath samples from 12 healthy adults, with measurements closely matching those obtained using gold-standard mass spectrometry. “These findings show that we have the high performance needed for applications such as clinical studies, where you really want to distinguish these slight differences in fat metabolism,” said Simone Hersberger, graduate student at ETH Zurich and first author of the study. 

The researchers then used the sensor to monitor breath acetone under four metabolic scenarios: light exercise followed by a high-carbohydrate meal, intense exercise followed by a high-carbohydrate meal, a high-fat ketogenic meal, and fasting. Breath acetone levels remained low during light exercise but increased with intense exercise, dropping after a high-carbohydrate meal. Acetone levels rose after a ketogenic meal and increased further during fasting. 

Through Alivion, a spin-off from ETH Zurich, the technology is already available to individuals interested in tracking breath acetone to monitor weight loss and athletic performance. The device is currently being used to monitor individual progress in clinical studies of epilepsy, where a ketogenic diet is a standard medical treatment. 

“Now it’s really time to spread it out into clinical trials and answer questions such as the effectiveness of different fasting therapies by providing personalized guidance,” said Güntner. “We’re really moving toward healthcare solutions that, in the future, you won’t need to go to the hospital for anymore. You’ll be able to do them at home.” 

The post Breath Sensor Monitors Fat Metabolism at Home appeared first on Inside Precision Medicine.

Malaria Drug Reveals Genetic Vulnerability Across Cancers

Scientists have found that the antimalarial drug quinacrine can exploit a vulnerability in cancers that become reliant on the NDRG1 protein to sustain their DNA damage response. Published in Science Signaling, their study not only identifies NDRG1 as a promising therapeutic target, but also demonstrates a new strategy for discovering similar vulnerabilities across multiple types of cancer.

“Our findings suggest that NDRG1 expression could serve as a biomarker to help identify patients most likely to benefit from therapies targeting this pathway,” said Garik V. Mkrtchyan, PhD, assistant professor at the University of Copenhagen and lead author of the study. “We further showed that high NDRG1 expression predicts poor survival across multiple cancers, and that inhibiting NDRG1 creates vulnerabilities, highlighting new opportunities for precision oncology.”

Mkrtchyan and colleagues set out to identify new targets for cancer therapeutics by leveraging the concept of synthetic lethality—a phenomenon where cancer cells can survive the loss of one of two genes but die when both are inhibited. This approach has already proven successful in ovarian, breast, and prostate cancers with BRCA mutations, which are particularly vulnerable to PARP inhibitor drugs. 

“In oncology, this concept is particularly promising because cancer cells often harbor mutations in specific DNA damage response pathways, making them highly dependent on the remaining repair mechanisms for survival,” said Mkrtchyan. “Targeting these dependencies enables selective elimination of cancer cells while sparing healthy tissue.”

Using transcriptomics data, the researchers identified quinacrine as a promising candidate for disrupting the DNA damage response by targeting the stress-response protein NDRG1. Quinacrine has been used as an antimalarial drug for nearly a century, later gaining approval as a treatment for lupus. In recent years, the compound has attracted growing interest as a potential cancer treatment. 

Screening through hundreds of cancer cell lines revealed that blood cancers, which generally showed high NDRG1 expression, were the most sensitive to the drug. Colorectal cancer cells were also sensitive to quinacrine, especially those with mutations in the MLH1 and PARP3 genes. The team later confirmed these findings in patient datasets, where high NDRG1 expression together with loss of either of these genes correlated with improved survival rates. 

“While quinacrine has previously been reported to possess anticancer activity, our study uncovers upstream mechanisms of its action on DNA damage response,” said Mkrtchyan. “By applying an automated robotics screen across more than 130 cancer cell lines, we identified novel synthetic lethal interactions involving NDRG1, providing a framework for discovering new therapeutic vulnerabilities across multiple cancer types.”

Despite its potential as a cancer therapy, quinacrine can potentially cause unwanted side effects. The researchers therefore plan to explore alternative drug candidates that can inhibit NDRG1 with more potency while reducing toxicity.

“The next steps will be to develop small molecules that inhibit NDRG1 with greater potency and specificity than quinacrine, thereby minimizing potential off-target effects,” said Mkrtchyan. “From a translational perspective, we aim to validate the identified synthetic lethal interactions in preclinical tumor models and investigate whether targeting the NDRG1 axis can overcome treatment resistance across a broader range of cancers.”

The post Malaria Drug Reveals Genetic Vulnerability Across Cancers appeared first on Inside Precision Medicine.

ctDNA Blood Test Better Targets Radiopharmaceutical Prostate Cancer Therapy

A new ctDNA blood test from a Japanese team identifies those metastatic, castration-resistant prostate cancer (mCRPC) patients most likely to benefit from 223Ra radiopharmaceutical therapy. The test also monitors their progress throughout treatment.

The study appeared in the July issue of The Journal of Nuclear Medicine. The lead author is Masaki Shiota, MD, PhD, associate professor in the Department of Urology in the Graduate School of Medical Sciences at Kyushu University in Fukuoka, Japan. 

Prostate cancer is very biologically heterogeneous. Patients who appear clinically similar may have different responses. Better tests are needed to match patients to therapies and determine the optimal treatment sequence or combination of therapies.

223Ra dichloride targets bone metastases and can improve overall survival and quality of life in CRPC patients. It is an alpha-particle–emitting radionuclide that behaves chemically like calcium. It is therefore preferentially incorporated into areas of increased bone turnover, including the osteoblastic lesions commonly produced by prostate cancer bone metastases.

But the treatment is expensive, clinical outcomes vary among patients, and there is not yet a reliable biomarker to predict or monitor treatment response.

This study used a research-based 88-gene panel with deep sequencing of plasma circulating tumor DNA (ctDNA) and matched leukocyte DNA. “The leukocyte analysis was important for distinguishing true tumor-derived alterations from germline variants and age-related clonal hematopoiesis,” Shiota told Inside Precision Medicine.  

Prostate cancer is one of the most commonly diagnosed malignancies in men. Metastatic castration-sensitive prostate cancer arises either de novo as a cancer, or as a recurrence after radical local therapy for localized disease. It accounts for approximately 10% of newly diagnosed prostate cancer cases in Japan.

This team tracked associations between ctDNA profiles and clinical outcomes, including biomarker response, radiographic progression-free survival, and overall survival. 

Patients with a higher amount of tumor DNA in the blood or certain gene changes, such as TP53, PTEN, and cell cycle pathway alterations, detected through ctDNA testing before treatment, had worse outcomes. Further, changes in tumor DNA reflected treatment response and disease trajectory.

“While 223Ra is an important treatment for prostate cancer that has spread to the bones, not all patients benefit equally,” said Shiota. “Our findings suggest that a blood-based genomic test may help identify patients who are more likely or less likely to benefit from the therapy. This could help doctors choose treatment more carefully and monitor patients more closely, with the goal of providing more personalized care.”

One of the biggest hurdles to the test’s advancement is reimbursement.

This depends on the country, the clinical indication, and the specific assay used. In Japan, Shiota explained, certain approved comprehensive genomic profiling tests using blood, such as FoundationOne Liquid CDx, can be covered by the national health insurance system under defined conditions. These tests are primarily used to identify potentially actionable alterations in patients with advanced solid tumors, particularly when obtaining adequate tumor tissue is difficult.

“The research assay used in our study is not currently reimbursed for selecting patients for radium-223 or for monitoring their response during treatment,” said Shiota. “Before insurance coverage could be considered for this particular use, our findings would need to be externally validated, and prospective studies would need to demonstrate that ctDNA-guided treatment decisions improve patient outcomes.”

ctDNA has several important applications in precision oncology. For example, it can: identify actionable genomic alterations and thereby help select targeted therapies, be used to monitor treatment response and detect emerging resistance mechanisms, capture tumor heterogeneity more comprehensively than a biopsy from a single metastatic site, detect minimal residual disease after treatment, and identify molecular relapse before it becomes apparent on conventional imaging.

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