Our Approach
“Precision medicine for cancer patients”
Telomeres are situated at the end of all chromosomes and prevent inappropriate triggering of the DNA repair mechanism.
Recent work in human epidemiology and evolutionary ecology suggests adult telomere length may reflect past physiological stress and predict subsequent morbidity and mortality, independent of chronological age. As cells divide, the telomeres shorten which may trigger cell senescence and apoptosis, but short telomeres are also prone to dysfunction and fusion which can lead to a state of cellular crisis characterized by large-scale genome instability and chromosome shattering – a process termed chromothripsis. These changes play a pivotal role in the aetiology and progression of human cancers.
Indeed, telomere dysfunction is thought to be one of the major drivers of carcinogenesis.