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Oncogenic bystander radiation effects in Patched heterozygous mouse cerebellum.

TitoloOncogenic bystander radiation effects in Patched heterozygous mouse cerebellum.
Tipo di pubblicazioneArticolo su Rivista peer-reviewed
Anno di Pubblicazione2008
AutoriMancuso, Mariateresa, Pasquali Emanuela, Leonardi Simona, Tanori Mirella, Rebessi Simonetta, Di Majo Vincenzo, Pazzaglia Simonetta, Toni Maria Pia, Pimpinella Maria, Covelli Vincenzo, and Saran Anna
RivistaProc Natl Acad Sci U S A
Volume105
Issue34
Paginazione12445-50
Data di pubblicazione2008 Aug 26
Parole chiaveAnimals, Animals, Newborn, Bystander Effect, cell communication, cerebellum, DNA damage, Gap Junctions, Genes, Tumor Suppressor, heterozygote, Mice, Neoplasms, patched receptors, Patched-1 Receptor, Radiation, Ionizing, Receptors, Cell Surface
Abstract

The central dogma of radiation biology, that biological effects of ionizing radiation are a direct consequence of DNA damage occurring in irradiated cells, has been challenged by observations that genetic/epigenetic changes occur in unexposed "bystander cells" neighboring directly-hit cells, due to cell-to-cell communication or soluble factors released by irradiated cells. To date, the vast majority of these effects are described in cell-culture systems, while in vivo validation and assessment of biological consequences within an organism remain uncertain. Here, we describe the neonatal mouse cerebellum as an accurate in vivo model to detect, quantify, and mechanistically dissect radiation-bystander responses. DNA double-strand breaks and apoptotic cell death were induced in bystander cerebellum in vivo. Accompanying these genetic events, we report bystander-related tumor induction in cerebellum of radiosensitive Patched-1 (Ptch1) heterozygous mice after x-ray exposure of the remainder of the body. We further show that genetic damage is a critical component of in vivo oncogenic bystander responses, and provide evidence supporting the role of gap-junctional intercellular communication (GJIC) in transmission of bystander signals in the central nervous system (CNS). These results represent the first proof-of-principle that bystander effects are factual in vivo events with carcinogenic potential, and implicate the need for re-evaluation of approaches currently used to estimate radiation-associated health risks.

DOI10.1073/pnas.0804186105
Alternate JournalProc. Natl. Acad. Sci. U.S.A.
Citation Key5073
PubMed ID18711141
PubMed Central IDPMC2517601