Authors: Rachel Jenkins, Future Science Group
Researchers at the University of Toronto (Toronto, Canada) have recently discovered that radiation therapy in childhood cancer survivors could trigger genomic structural rearrangements leading to radiation-induced meningioma (RIM) in adulthood and highlighting a potential therapy target.
Recently published in Nature Communications, the study was carried out by co-investigators Gelareh Zadeh and Ken Aldape, both at the University of Toronto. The biological differences between RIMs and sporadic meningiomas (SMs) were investigated and it was discovered that that RIM was distinct in its mutational profile when compared with SM.
The most common type of adult brain tumor, meningioma, can develop in childhood cancer survivors after their treatment with cranial radiation. Zadeh commented: “By understanding the biology, the goal is to identify a therapeutic strategy that could be implemented early on after childhood radiation to prevent the formation of these tumours in the first place.”
A total of 31 RIM patients, 74% of which were leukaemia or medulloblastoma survivors, were compared and contrasted against a control group of 30 SMs. First, the team discovered that established mutations in SM were not observed in RIMs.
Second, the researchers reported that 12 out of 31 RIMs were found to have an NF2 gene rearrangement, which had previously not been reported in SM. In particular, the fusion frame NF2-DDX49 is hypothesized to contain oncogenic properties. Following on from this, the researchers suggested that radiation therapy could trigger genomic structural rearrangements through error-prone repair of double strand DNA breaks.
Due to current therapeutic targets for SM not being present in the RIM cohort, the findings present a potential target against these meningiomas, and suggest that effective therapies for childhood cancer survivors may differ from those targeting SM.
Aldape concluded: “Our research identified a specific rearrangement involving the NF2 gene that causes radiation-induced meningiomas. But there are likely other genetic rearrangements that are occurring as a result of that radiation-induced DNA damage. So one of the next steps is to identify what the radiation is doing to the DNA of the meninges.”
Further adding: “In addition, identifying the subset of childhood cancer patients who are at highest risk to develop meningioma is critical so that they could be followed closely for early detection and management.”
Sources: Agnihotri S, Suppiah S, Tonge P et al. Therapeutic radiation for childhood cancer drives structural aberrations of NF2 in meningiomas. Nat. Comms. 8(1) (2017); www.uhn.ca/corporate/News/PressReleases/Pages/brain-tumour-scientists-map-mutation-that-drives-tumours-in-childhood-cancer-survivors-treated-with-radiation-decades-earl.aspx