Ever since the 1960s, the medical world has wondered why some patients who suffer from illnesses resulting from inadequate cell division are much more susceptible to cancer which is conversely characterized by excessive cell division. The Laboratory for Disease Mechanisms in Cancer has now succeeded in unravelling the mechanism of how defective ribosomes can cause both insufficient and excessive cell division.
How can those diseases that are caused by too few cells later turn into diseases caused by too many cells’ This unsolved paradox - also known as Dameshek’s Riddle - has puzzled the scientific community for years. Ever since the 1960s, the medical world has wondered why some patients who suffer from illnesses resulting from inadequate cell division are much more susceptible to cancer which is conversely characterized by excessive cell division.
A number of these diseases are related to defects in the essential cellular protein factories, ribosomes, and are aptly named ribosomopathies. The cells in ribosomopathy patients do not divide enough, resulting in a very broad spectrum of cellular insufficiency symptoms, from anaemia to growth retardation. While treatments for some of these symptoms do exist, the increased likelihood of developing cancer makes these disorders particularly challenging to understand and cure.
The Laboratory for Disease Mechanisms in Cancer in Leuven has now succeeded in unravelling the mechanism of how defective ribosomes can cause both insufficient and excessive cell division. "Defects in ribosomes have two different consequences for the cells. On the one hand, the defective ribosomes make specific kinds of mistakes which leads to the increased production of the proteins that nourish cancer cells. At the same time, these ribosome defects cause a build-up of toxic substances that damage the cells, forcing them to grow and divide less. The cell suffers from several different kinds of damage, including DNA damage. This in turn causes mutations," explains Professor Kim De Keersmaecker, head of the Laboratory for Disease Mechanisms in Cancer.
In a later, second phase, the cellular balance is starting to shift. "All these mutations will eventually include one that is able to compensate for the cell damage and "rescue" the cell, allowing cell division to increase. At that point, cancer cells can take advantage of the high availability of proteins that favour their growth. This opens the floodgates, with ever-increasing cancer protein levels and even better "rescuing" mutations protecting cells from damage. This allows a tumour to grow in an uncontrolled way."
This study provides a solution to the enigmatic Dameshek’s Riddle with regard to ribosome defects. The discovery of this new paradigm also turns ribosome defects into an attractive target in the fight against cancer, explains De Keersmaecker: "We see these defects both in congenital and non-congenital cancers. And now we also know that ribosome defects can give rise to a whole series of additional cellular defects. In other words, if we can tackle the cause, we can prevent many of the downstream problems. This is the research track we are currently exploring."