Tuesday, February 03, 2026

 

Surgical innovation cuts ovarian cancer risk by nearly 80%



New UBC research shows that a simple surgical add-on can dramatically reduce rates of the most lethal gynaecological cancer




University of British Columbia





A prevention strategy developed by Canadian researchers can reduce the risk of the most common and deadly form of ovarian cancer by nearly 80 per cent, according to a new study published today in JAMA Network Open by researchers at the University of British Columbia (UBC). 

The strategy, known as opportunistic salpingectomy (OS), involves proactively removing a person’s fallopian tubes when they are already undergoing a routine gynaecological surgery such as hysterectomy or tubal ligation, commonly called “having one’s tubes tied”.  

The Canadian province of British Columbia (B.C.) became the first jurisdiction in the world to offer OS in 2010, after a team of researchers from UBC, BC Cancer and Vancouver Coastal Health designed the approach when it was discovered that most ovarian cancers originate in the fallopian tubes rather than the ovaries. OS leaves a person’s ovaries intact, preserving important hormone production so there are minimal side effects from the added procedure.  

The new study, led by a B.C.-based international collaboration called the Ovarian Cancer Observatory, provides the clearest evidence yet that the Canadian innovation saves lives. 

“This study clearly demonstrates that removing the fallopian tubes as an add-on during routine surgery can help prevent the most lethal type of ovarian cancer,” said co-senior author Dr. Gillian Hanley, an associate professor of obstetrics and gynaecology at UBC. “It shows how this relatively simple change in surgical practice can have a profound and life-saving impact.”  

New hope against a deadly cancer 

Ovarian cancer is the most lethal gynaecological cancer. Approximately 3,100 Canadians are diagnosed with the disease each year and about 2,000 will die from it.   

There is currently no reliable screening test for ovarian cancer, meaning that most cases are diagnosed at advanced stages when treatment options are limited and survival rates are low. 

The OS approach was initially developed and named by Dr. Dianne Miller, an associate professor emerita at UBC and gynaecologic oncologist with Vancouver Coastal Health and BC Cancer. She co-founded B.C.’s multidisciplinary ovarian cancer research team, OVCARE.  

"If there is one thing better than curing cancer it's never getting the cancer in the first place," said Dr. Miller.   

The new study is the first to quantify how much OS reduces the risk of serous ovarian cancer—the most common and deadly subtype of the disease. It builds on previous research demonstrating that OS is safe, does not reduce the age of menopause onset, and is cost-effective for health systems. 

The study analyzed population-based health data for more than 85,000 people who underwent gynaecological surgeries in B.C. between 2008 and 2020. The researchers compared rates of serous ovarian cancer between those who had OS and those who had similar surgeries but did not undergo the procedure.  

Overall, people who had OS were 78 per cent less likely to develop serous ovarian cancer. In the rare cases where ovarian cancer occurred after OS, those cancers were found to be less biologically aggressive. The findings were validated by data collected from pathology laboratories from around the world, which suggested a similar effect. 

From B.C. innovation to global impact 

Since its introduction in B.C. in 2010, OS has been widely adopted, with approximately 80 per cent of hysterectomies and tubal ligation procedures in the province now including fallopian tube removal. 

Globally, professional medical organizations in 24 countries now recommended OS as an ovarian cancer prevention strategy, including the Society of Obstetrics and Gynaecology of Canada, which issued guidance in 2015.   

“This is the culmination of more than a decade of work that started here in B.C.,” said co- senior author Dr. David Huntsman, professor of pathology and laboratory medicine and obstetrics and gynaecology at UBC and a distinguished scientist at BC Cancer. “The impact of OS that we report is even greater than we expected.”  

The researchers say expanding global adoption of OS could prevent thousands of ovarian cancer cases worldwide each year.  

Extending OS to other abdominal and pelvic surgeries where appropriate could further increase the number of people who could benefit from the prevention strategy. B.C. recently became the first province to expand OS to routine surgeries performed by general and urologic surgeons through a project supported by the Government of B.C. and Doctors of BC.  

“Our hope is that more clinicians will adopt this proven approach, which has the potential to save countless lives,” said Dr. Huntsman. “Not offering this surgical add-on may leave patients unnecessarily vulnerable to this cancer.” 

Interview language(s): English 

 

New discovery sheds light on evolutionary crossroads of vertebrates   




University of St. Andrews
Juvenile Ciona Seasquirt 

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Juvenile Ciona Seasquirt

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Credit: Shunsuke Sogabe





New research from the University of St Andrews has discovered a crucial piece in the puzzle of how all animals with a spine - including all mammals, fish, reptiles and amphibians - evolved.   

In a paper published today (2nd February) in BMC Biology, researchers found an intriguing pattern of gene evolution which appears to be significant for the evolutionary origin and diversification of vertebrates.   

All animals have major signalling pathways that their cells use to communicate with each other, which control things like how their embryos and organs develop. The signalling pathways are fundamental to animal development and are major targets in disease-causing mutations and for the development of pharmaceuticals.   

Proteins at the base of these signalling pathways are crucial as they control the final output from them, like a traffic system, directing cells into specific responses and gene expression.   

Researchers created new gene sequencing data in sea squirts, a lamprey and a type of frog. They found the genes that make these signalling output proteins have evolved in a distinctive way. The sea squirt is an invertebrate that helped to distinguish the change when moving from invertebrates to vertebrates. Lampreys are an early branch in the vertebrate group, which pinpoints that this change happened at the invertebrate-to-vertebrate transition.  

Researchers used long-molecule DNA sequencing, which allowed them to distinguish the different transcripts from each gene. Long-molecule sequencing had never been done on the genes expressed in these particular animals before. Therefore, researchers were able to characterise the real range of the transcripts and proteins produced from these genes in vertebrate development for the first time ever.  

Unlike the invertebrate sea squirt, the lamprey and frog made higher numbers of different forms of proteins from the individual signalling output genes, compared to all sorts of other types of genes.    

This significant change with the evolution of vertebrates is very striking. Given the importance of these pathways in how animals decide what types of cells, tissues and organs to make, it is highly likely these proteins have had a major role in making vertebrates (animals with backbones) different and more complex than invertebrates.   

Lead author of the study Professor David Ferrier from the School of Biology, said: “It was very surprising to us to see how this small selection of very particular genes stands out in the way that they are behaving compared to any other sort of gene we looked at.It will be exciting to determine how these various different protein forms work in distinct ways to generate the diversity of cell types we now see in vertebrates.”  

These diverse protein variations not only shed light on the origins of how we, and most other animals with backbones have evolved, but will also be important for future work on understanding how these proteins and pathways might be manipulated in disease management.  

 ENDS 

  

Adult Lamprey

Credit

Sebastian Shimeld



Xenopus Tadpole

Credit

Marika Salonna

 

Aging researchers find new puzzle piece in the game of longevity



The lab of Kris Burkewitz just made a key discovery: How cellular machineries are structured and organized within a cell has implications for healthy aging. “We didn't just add a piece to the puzzle—we found a whole section that hasn't even been touch



Vanderbilt University

ER-phagy 

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The discovery that ER-phagy is involved in aging highlights this process as a possible drug target for age-related chronic conditions such as neurodegenerative diseases and various metabolic disease contexts.

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Credit: Burkewitz et. al.




The idea

Improvements in public health have allowed humankind to survive to older ages than ever before, but, for many people, these added golden years are not spent in good health. Aging is a natural part of life, but it is associated with a greatly increased incidence of most chronic diseases, including various cancers, diabetes, and Alzheimer’s disease.

The laboratory of Kris Burkewitz, assistant professor of cell and developmental biology, wants to figure out if there is a way to break the links between the aging process and disease so that we can stay healthy longer, allowing us to better enjoy our later years. To accomplish this goal, the Burkewitz lab focuses on how cells organize their internal compartments, or organelles, and how organelle structures can influence cellular function, metabolism, and disease risk.

In his most recent paper, published in Nature Cell Biology, Burkewitz describes a new way by which cells adapt to the aging process: by actively remodeling the endoplasmic reticulum, one of the cell’s largest and most complex organelles. His team found that aging cells remodel their ER through a process called ER-phagy, which selectively targets specific ER subdomains for breakdown. The discovery that ER-phagy is involved in aging highlights this process as a possible drug target for age-related chronic conditions such as neurodegenerative diseases and various metabolic disease contexts.

What we knew

“Where many prior studies have documented how the levels of different cellular machineries change with age, we are focusing instead on how aging affects the way that cells house and organize these machineries within their complex inner architectures,” Burkewitz said.

The efficiency of a cell’s function and metabolism depends on how those collections of machineries are organized and distributed within a cell. A helpful way to envision how the inner architecture of a cell impacts its function is to imagine a factory that builds many complex products. According to Burkewitz, that factory needs a lot of specialized machineries, but even if all they are all present, the factory only runs smoothly if they are arranged in the right position and sequence. “When space is limited or production demands change, the factory has to reorganize its layout to make the right products,” Burkewitz said. “If organization breaks down, production becomes very inefficient.”

One of the largest and most important structures in a cell is the ER, a labyrinth of interconnected sheets and tubules that not only acts as a major production hub for proteins and lipids but serves as a scaffold for organizing other parts of the cell. Despite these critical roles, scientists knew surprisingly little about how the structure of the ER might change in aging animals.

What we found out

“We didn’t just add a piece to the aging puzzle—we found a whole section that hasn’t even been touched,” said Eric Donahue, PhD’25, the first author of the paper. Donahue is a medical student in the Medical Scientist Training Program who recently completed the Ph.D. portion of his training in the Burkewitz lab, where he focused on ER-phagy, ER remodeling, and aging.

Donahue, Burkewitz, and their team used new genetic tools and advanced light and electron microscopy to visualize how the ER is shaped and organized inside cells of living Caenorhabditis elegans worms, a widely used model for aging research. C. elegans worms possess a unique combination of characteristics that make them the ideal model to study aging: They are transparent and age rapidly, a combination that allows researchers to observe what happens inside the cells of intact, aging animals.

Burkewitz and his team found that, as animals age, they dramatically reduce the amount of “rough” ER in their cells, which is involved in creating more protein; the amount of tubular ER, which is more closely associated with lipid or fat production, is only slightly impacted. This change fits with broader themes of aging, including declines in our ability to maintain functional proteins and shifts in metabolism that lead us to accumulate fat in new places; more research is needed to establish these links causally.

The researchers also found that cells use the process of ER-phagy to remodel their ER during aging and that ER-phagy is linked to lifespan, actively contributing to healthy aging.

What’s next?

The Burkewitz lab will continue to probe the different structures of the ER and how they can promote different metabolic outputs at the cell and whole-animal scales. As the ER is one of the master controllers for organizing all other compartments within the cell, it will be important to ask how its remodeling during aging impacts the organization of other cellular components. “Changes in the ER occur relatively early in the aging process,” Burkewitz said. “One of the most exciting implications of this is that it may be one of the triggers for what comes later: dysfunction and disease.”

If scientists can figure out what, exactly, is the trigger, they may be able to stop it from firing.

Here’s to a long, healthy life for us all! Thank you, science.

Go deeper

The paper “ER remodeling is a feature of aging and depends on ER-phagy” was published in Nature Cell Biology in February 2026.

This work was performed in collaboration with the Vanderbilt University labs of Jason MacGurn, associate professor of cell and developmental biology, Andrew Folkmann, assistant professor of biochemistry, Rafael Arrojo e Drigo, assistant professor of molecular physiology and biophysics, and Lauren Jackson, associate professor of biological sciences, plus collaborators from the University of Michigan and the University of California, San Diego.

Funding

This research was supported by funds from the National Institute on Aging, the National Institute of General Medical Sciences, and the Glenn Foundation for Medical Research/American Federation for Aging Research.

School of Medicine Basic Sciences shared resources

This research made use of the Cell Imaging Shared Resource.

ER Phagy 

Vanderbilt University