The findings were published in Nature Communications. The research was led by AnnaLynn Williams, PhD, of the University of Rochester Wilmot Cancer Institute, along with co-corresponding author Kevin Krull, PhD, of St. Jude Children’s Research Hospital.

Lifestyle Changes May Help Reverse Biological Aging

There may be encouraging news ahead. Ongoing work at Wilmot suggests that some of the accelerated aging seen in young survivors could potentially be slowed or even reversed through healthy habits such as quitting smoking, exercising regularly, and improving diet, Williams said.

“Young cancer survivors have many more decades of life to live,” she said. “So, if these accelerated aging changes are occurring early on and setting them on a different trajectory, the goal is to intervene to not only increase their lifespan but improve their quality of life.”

Many survivors treated in childhood or young adulthood are working toward finishing school, launching careers, gaining independence, or starting families. Cognitive challenges can make those milestones harder to reach.

“It’s kind of like a perfect storm,” Williams said. “This is why we see many survivors having worse educational and employment outcomes than their siblings.”

Williams, who is also a cancer survivor, serves as an assistant professor in the Department of Surgery and is part of Wilmot’s Cancer Prevention and Control research program, which focuses on reducing long-term symptoms in survivors.

Study Tracks Long Term Survivors

The study included about 1,400 participants treated at St. Jude. All were at least five years beyond their cancer therapy, and some had survived for decades. Most had been treated for acute lymphoblastic leukemia (ALL) or Hodgkin lymphoma.

Researchers found evidence of faster biological aging regardless of the type of treatment received during childhood. However, chemotherapy was linked to the greatest acceleration. Because chemotherapy can alter DNA structure and cause widespread cellular damage, it appears to have the strongest effect on the aging process.

Biological Age Linked to Brain Function

The investigators also identified a close connection between cellular aging and cognitive performance. Survivors whose biological age was higher than their actual chronological age had more difficulty with memory and attention.

For individuals who received radiation directly to the brain, Williams said the priority is preventing further decline.

Scientists are now trying to pinpoint when accelerated aging begins. That research is ongoing at Wilmot.

In a recent pilot study, Williams examined tissue and cell samples taken before and after treatment from 50 people with Hodgkin lymphoma and compared them with samples from 50 healthy individuals. Working with John Ashton, PhD, MBA, director of the Genomics Shared Resource at Wilmot, she analyzed the data to determine whether the aging process starts during treatment or develops years later.

Other Wilmot researchers are carrying out related studies in women with breast cancer and in older adults with leukemia, aiming to find ways to reverse treatment-related aging. One recent study has already demonstrated that exercise can help counteract aging linked to cancer.

The National Cancer Institute funded Williams’ study.

At the same time, researchers have repeatedly observed high levels of polyamines in many types of cancer, where they are linked to aggressive tumor growth. This contrast has created a scientific puzzle. How can the same molecules that appear to promote longevity also be associated with cancer?

A Molecular Puzzle in Cancer Metabolism

Although the connection between polyamines and cancer has been recognized for years, the detailed mechanisms behind their role in tumor progression have remained unclear. Cancer cells are known to alter their metabolism, relying heavily on aerobic glycolysis to rapidly generate energy. However, exactly how polyamines influence this metabolic shift has not been fully understood.

Adding to the complexity, eIF5A1 has well established functions in normal, healthy cells. A closely related protein, eIF5A2, shares 84% of its amino acid sequence but has been linked to cancer development. Why two nearly identical proteins behave so differently has been a major unanswered question.

Large Scale Proteomic Analysis Reveals Distinct Pathways

To investigate, a team led by Associate Professor Kyohei Higashi from the Faculty of Pharmaceutical Sciences at Tokyo University of Science in Japan carried out an in-depth study using advanced molecular and proteomic methods. Their results were published in Volume 301, Issue 8 of the Journal of Biological Chemistry. The findings clarify how polyamines stimulate cancer cell growth through biological routes that differ from those involved in healthy aging.

The researchers worked with human cancer cell lines to examine how polyamines affect protein production and metabolism. They first reduced polyamine levels using a drug, then restored them by adding spermidine. This approach allowed them to directly measure the impact of polyamines on cancer cells. Using high-resolution proteomic techniques, they analyzed changes across more than 6,700 proteins.

Their results showed that polyamines primarily boost glycolysis, the process that quickly converts glucose into energy, rather than enhancing mitochondrial respiration, which is more closely tied to healthy aging. The team also found that polyamines increase levels of eIF5A2 and five ribosomal proteins, including RPS 27A, RPL36AL, and RPL22L1, all of which are associated with cancer severity.

eIF5A1 vs eIF5A2 in Normal and Cancer Cells

A side by side comparison of eIF5A1 and eIF5A2 provided critical insight. “The biological activity of polyamines via eIF5A differs between normal and cancer tissues,” explains Dr. Higashi. “In normal tissues, eIF5A1, activated by polyamines, activates mitochondria via autophagy, whereas in cancer tissues, eIF5A2, whose synthesis is promoted by polyamines, controls gene expression at the translational level to facilitate the proliferation of cancer cells.”

In other words, polyamines trigger very different effects depending on which protein they influence. In healthy cells, they support cellular maintenance and energy production. In cancer cells, they help drive rapid growth.

How Polyamines Increase eIF5A2

Further experiments uncovered how polyamines raise eIF5A2 levels. Under typical conditions, production of the eIF5A2 protein is restrained by a small regulatory RNA molecule called miR-6514-5p. The researchers found that polyamines disrupt this natural brake, allowing eIF5A2 to be produced in greater amounts. They also showed that eIF5A2 controls a distinct group of proteins compared to eIF5A1, reinforcing the idea that these two similar proteins carry out separate functions.

Implications for Cancer Therapy and Supplement Safety

These findings carry important implications for both cancer treatment and the use of polyamine supplements. The results highlight how strongly biological context matters. In healthy tissues, polyamines may provide anti-aging benefits through eIF5A1. In tissues that are cancerous or at risk of becoming malignant, the same molecules can stimulate tumor growth through eIF5A2. This dual behavior helps explain why polyamines have been so challenging to interpret in medical research.

The study also identifies a promising new therapeutic target. “Our findings reveal an important role for eIF5A2, regulated by polyamines and miR-6514-5p, in cancer cell proliferation, suggesting that the interaction between eIF5A2 and ribosomes, which regulates cancer progression, is a selective target for cancer treatment,” remarks Dr. Higashi. Targeting eIF5A2 specifically could, in theory, slow cancer growth without interfering with the beneficial effects linked to eIF5A1.

Overall, this research marks a significant advance in understanding the complex and sometimes contradictory roles of polyamines. In the future, scientists may be able to design strategies that preserve their positive effects on healthy aging while reducing their potential to support cancer development.

This study was supported in part by a Grant-in-Aid for Scientific Research (C) (No. 18K06652) from the Japan Society for the Promotion of Science, the Hamaguchi Foundation for the Advancement of Biochemistry, and an Extramural Collaborative Research Grant of the Cancer Research Institute, Kanazawa University, Japan.

Now researchers report in Nature Nanotechnology that magnetism can also behave in surprising ways under these conditions. In twisted antiferromagnetic layers, magnetic spin patterns are not limited to the small repeating moiré unit cell. Instead, they can spread into much larger, topological structures that extend across hundreds of nanometers.

Giant Magnetic Textures Beyond the Moiré Pattern

In most moiré systems, the size of physical effects is determined directly by the interference pattern created when two crystal lattices overlap. Magnetic order in stacked van der Waals magnets was widely expected to follow this same length scale. The new findings challenge that assumption.

The team examined twisted double bilayer chromium triiodide (CrI₃) using scanning nitrogen-vacancy magnetometry, a technique that images magnetic fields with nanoscale precision. They observed magnetic textures reaching distances of up to ~300 nm, far exceeding the size of a single moiré cell and roughly ten times larger than the underlying wavelength.

A Counterintuitive Twist Angle Effect

The results reveal an unexpected pattern. When the twist angle becomes smaller, the moiré wavelength increases. However, the magnetic textures do not simply grow along with it. Instead, their size changes in the opposite way, reaching a maximum near 1.1° and disappearing above ~2°.

This reversal shows that magnetism is not just copying the moiré template. Rather, it arises from a balance between several competing forces, including exchange interactions, magnetic anisotropy and Dzyaloshinskii-Moriya interactions. All of these are subtly adjusted by how the layers are rotated relative to one another. Large scale spin dynamics simulations back up this interpretation, demonstrating the formation of extended Néel-type antiferromagnetic skyrmions that span multiple moiré cells.

Skyrmions and Low Power Spintronics

These findings matter beyond basic physics. Skyrmions are promising for future information technologies because they are small, stable and protected by their topology. They can also be moved using very little energy. Creating them simply by adjusting the twist angle, without lithography, heavy metals or strong electric currents, provides a clean and geometry driven path toward low power spintronic devices.

The researchers describe this phenomenon as super-moiré spin order, highlighting that twist engineering operates across multiple scales. A change in atomic alignment can generate topological structures on much larger, mesoscale distances. This challenges the long held idea that moiré physics is only a local effect and positions twist angle as a powerful thermodynamic control parameter capable of tuning exchange, anisotropy and chiral interactions to stabilize topological phases.

From a practical standpoint, these large and robust Néel-type skyrmionic textures are well suited for integration into devices. Their larger size makes them easier to detect and manipulate. At the same time, their topological protection and insulating host material suggest extremely low energy loss during operation. As scientists continue to explore how geometry shapes quantum behavior, such emergent magnetic states could play an important role in developing energy efficient, post-CMOS computing technologies.

Dr. Elton Santos, Reader in Theoretical/Computational Condensed Matter Physics, University of Edinburgh, whose team led the modelling aspect of the project, said: “This discovery shows that twisting is not just an electronic knob, but a magnetic one. We’re seeing collective spin order self-organize on scales far larger than the moiré lattice. It opens the door to designing topological magnetic states simply by controlling angle, which is a remarkably simple handle with profound practical consequences.”