A previously unknown mechanism that makes it possible for aggressive so-called triple-negative breast cancer to fine-tune its production of proteins has been discovered by researchers at Umeå University, Sweden. The discovery increases our understanding of how tumours grow and adapt, and it opens up for research into new future treatments.
"We have found a critical control point that, when disturbed, can tip the balance against cancer," says Francesca Aguilo, associate professor at the Department of Molecular Biology at Umeå University and who has led the current study.
All cells in the body use ribosomes, small molecular factories, to translate genetic information from RNA into proteins. Ribosomes are complex structures made up of ribosomal RNA and proteins, and they have built-in control systems that ensure that everything works as it should. When these systems are disrupted, diseases such as cancer can occur.
Ribosomal RNA is rich in chemical modifications that help the ribosome function optimally. One such modification is 2′-O-methylation, Nm, which is controlled by the enzyme fibrillarin. The new study shows that fibrillarin plays a key role in how ribosomes are built and which proteins are made.
The researchers discovered that fibrillarin collaborates with the ribosome protein RPS28 to create specialized ribosomes with unique properties. When fibrillarin is missing, RPS28 also disappears, leading to a mixture of different ribosome types – so-called ribosomal heterogeneity. This imbalance affects which proteins are produced and can drive the development of cancer.
"Cancer is not only about mutated genes, but also about how cells control the amount and type of proteins that are produced," says Francesca Aguilo.
Although more research is needed before the results can be translated into treatments, the study points to a new direction for research on treatments; to attack cancer as a disease of misregulated protein production.
Cancer Letters
Experimental study
Cells
Fibrillarin-dependent 2'-O-methylation modulates RPS28 ribosome incorporation and oncogenic translation
17-Nov-2025