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First study to date to investigate cancer risk in mosaic RASopathies due to disease-causing variants in the HRAS or KRAS genes shows the importance of close cancer surveillance.
Hereditary changes in genes are often the cause of rare diseases. For example, disease-causing gene variants (PVs) in the HRAS gene cause Costello syndrome and PVs in the KRAS gene cause Noonan syndrome and cardio-facio-cutaneous syndrome. If such PVs only arise during embryonic development in the womb, those affected suffer from a mosaic disease in which both altered and healthy cells are present. In this context, researchers at the Hannover Medical School (MHH) and the National Cancer Institute (NCI) in the USA have for the first time analysed the cancer risk within a special group of young patients. The results make it clear how important close cancer monitoring is, with 20 per cent of those affected being diagnosed with cancer by the age of just 20. Looking at rhabdomyosarcoma alone, the risk of developing the disease was 800 times higher than in the population as a whole.
Special high-risk group
‘We were able to include a total of 69 cases in the study. We observed twelve cancers, mainly in young children,’ explains Professor Dr. Christian Kratz, Director of the Department of Paediatric Haematology and Oncology at the MHH and initiator of the study. Professor Kratz's team only included patients with multi-line mosaic RASopathies in the study. RASopathies are a group of developmental disorders caused by a dysregulation in genes of the RAS-MAPK signalling pathway. The study analysed PVs in the HRAS or KRAS gene.
‘A special feature of mosaic RASopathies is that they are disorders that only develop in the embryo during embryonic development. PVs can occur at any time during pregnancy. In this case, we speak of a mosaic, since not all cells carry the change,’ explains Gina Ney, a researcher at the NCI in the USA. In the case of PVs that occurred early during embryonic development, different tissues are affected by the mosaic RASopathy. They are referred to in the study as multilineage mosaic RASopathies.
Genetic alterations as a driving force for cancer
The spectrum of PVs typically found in mosaic RASopathies overlaps with the spectrum of gene mutations found in cancers. Rhabdomyosarcomas were diagnosed in seven patients. The patients were between one and 48 months old, with one case of rhabdomyosarcoma detected at twelve years of age. ‘It is noteworthy that all seven rhabdomyosarcomas occurred in the urogenital region. This is an important finding that is particularly relevant for the clinical care of those affected,’ says Jonas Windrich, a medical student at the MHH who was involved in the study as co-first author. Furthermore, three cases of skin cancer, one Wilms tumour and one case of bladder cancer were observed.
Close cancer monitoring required
The highest cancer risk was observed in the first years of life. ‘There is a particular need for rigorous rhabdomyosarcoma early detection in young children. Regular skin cancer screening is required for adults with this high-risk disease,’ emphasises Stewart, a researcher at the NCI in the USA.
Professor Dr. Christian Kratz, Kratz.Christian@mh-hannover.de, telephone +49 511 532-6712
https://aacrjournals.org/clincancerres/article/doi/10.1158/1078-0432.CCR-24-1928...
The researchers Professor Dr. Christian Kratz and Jonas Windrich have analysed the cancer risk in pa ...
Jana Illmer
Jana Illmer/MHH
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The researchers Professor Dr. Christian Kratz and Jonas Windrich have analysed the cancer risk in pa ...
Jana Illmer
Jana Illmer/MHH
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