bioRxiv · 10.1101/2022.01.25.477771
The ALT pathway generates telomere fusions that can be detected in the blood of cancer patients
Abstract
Telomere fusions (TFs) can trigger the accumulation of diverse genomic rearrangements and the acquisition of oncogenic alterations leading to malignant transformation and resistance to chemotherapy. Despite their relevance in tumour evolution, our understanding of the patterns and consequences of TFs in human cancer remains limited. Here, we have characterized the rates and spectrum of somatic TFs across >30 cancer types using whole-genome sequencing data. TFs are pervasive in human tumours with rates varying markedly across and within cancer types. In addition to end-to-end fusions, we find novel patterns of TFs that we mechanistically link to the activity of the alternative lengthening of telomeres (ALT) pathway. We show that TFs can be detected in the blood of cancer patients, which enables cancer detection with high specificity and sensitivity even for early-stage tumours and cancer types for which early detection remains a high unmet clinical need, such as pancreatic cancer and brain tumours. Overall, we report a novel genomic footprint that enables characterization of the telomere maintenance mechanism of tumours and liquid biopsy analysis, which has implications for early detection, prognosis, and treatment selection.
Source connections
Explore related subjects
Keep this discovery
Explore connections, maps & timelines
Muyas, F., Gomez Rodriguez, M. J., Cortes-Ciriano, I., Flores, I.. 2022-01-28. The ALT pathway generates telomere fusions that can be detected in the blood of cancer patients. https://doi.org/10.1101/2022.01.25.477771
Cite the original work for its findings. Save a collection to share your selection of sources.