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Keywords = retinal astrocytoma

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14 pages, 956 KiB  
Article
Eye Tumors in Childhood as First Sign of Tumor Predisposition Syndromes: Insights from an Observational Study Conducted in Germany and Austria
by Madlen Reschke, Eva Biewald, Leo Bronstein, Ines B. Brecht, Sabine Dittner-Moormann, Frank Driever, Martin Ebinger, Gudrun Fleischhack, Desiree Grabow, Dirk Geismar, Sophia Göricke, Maja Guberina, Claudia H. D. Le Guin, Tobias Kiefer, Christian P. Kratz, Klaus Metz, Bert Müller, Tatsiana Ryl, Marc Schlamann, Sabrina Schlüter, Stefan Schönberger, Johannes H. Schulte, Selma Sirin, Daniela Süsskind, Beate Timmermann, Saskia Ting, Werner Wackernagel, Regina Wieland, Martin Zenker, Michael Zeschnigk, Dirk Reinhardt, Angelika Eggert, Petra Ritter-Sovinz, Dietmar R. Lohmann, Norbert Bornfeld, Nikolaos Bechrakis and Petra Ketteleradd Show full author list remove Hide full author list
Cancers 2021, 13(8), 1876; https://doi.org/10.3390/cancers13081876 - 14 Apr 2021
Cited by 12 | Viewed by 3739
Abstract
Retinoblastoma and other eye tumors in childhood are rare diseases. Many eye tumors are the first signs of a genetic tumor predisposition syndrome and the affected children carry a higher risk of developing other cancers later in life. Clinical and genetic data of [...] Read more.
Retinoblastoma and other eye tumors in childhood are rare diseases. Many eye tumors are the first signs of a genetic tumor predisposition syndrome and the affected children carry a higher risk of developing other cancers later in life. Clinical and genetic data of all children with eye tumors diagnosed between 2013–2018 in Germany and Austria were collected in a multicenter prospective observational study. In five years, 300 children were recruited into the study: 287 with retinoblastoma, 7 uveal melanoma, 3 ciliary body medulloepithelioma, 2 retinal astrocytoma, 1 meningioma of the optic nerve extending into the eye. Heritable retinoblastoma was diagnosed in 44% of children with retinoblastoma. One child with meningioma of the optic nerve extending into the eye was diagnosed with neurofibromatosis 2. No pathogenic constitutional variant in DICER1 was detected in a child with medulloepithelioma while two children did not receive genetic analysis. Because of the known association with tumor predisposition syndromes, genetic counseling should be offered to all children with eye tumors. Children with a genetic predisposition to cancer should receive a tailored surveillance including detailed history, physical examinations and, if indicated, imaging to screen for other cancer. Early detection of cancers may reduce mortality. Full article
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13 pages, 6206 KiB  
Article
The Rescue and Characterization of Recombinant, Microcephaly-Associated Zika Viruses as Single-Round Infectious Particles
by Chien-Yi Lu, Chen-Sheng Lin, Hsueh-Chou Lai, Ya-Wen Yu, Chih-Yi Liao, Wen-Chi Su, Bo-Han Ko, Young-Sheng Chang, Su-Hua Huang and Cheng-Wen Lin
Viruses 2019, 11(11), 1005; https://doi.org/10.3390/v11111005 - 31 Oct 2019
Cited by 10 | Viewed by 3457
Abstract
Zika virus (ZIKV) is transmitted by Aedes mosquitoes and exhibits genetic variation with African and Asian lineages. ZIKV Natal RGN strain, an Asian-lineage virus, has been identified in brain tissues from fetal autopsy cases with microcephaly and is suggested to be a neurotropic [...] Read more.
Zika virus (ZIKV) is transmitted by Aedes mosquitoes and exhibits genetic variation with African and Asian lineages. ZIKV Natal RGN strain, an Asian-lineage virus, has been identified in brain tissues from fetal autopsy cases with microcephaly and is suggested to be a neurotropic variant. However, ZIKV Natal RGN strain has not been isolated; its biological features are not yet illustrated. This study rescued and characterized recombinant, single-round infectious particles (SRIPs) of the ZIKV Natal RGN strain using reverse genetic and synthetic biology techniques. The DNA-launched replicon of ZIKV Natal RGN was constructed and contains the EGFP reporter, lacks prM-E genes, and replicates under CMV promoter control. The peak in the ZIKV Natal RGN SRIP titer reached 6.25 × 106 TCID50/mL in the supernatant of prM-E-expressing packaging cells 72 h post-transfection with a ZIKV Natal RGN replicon. The infectivity of ZIKV Natal RGN SRIPs has been demonstrated to correlate with the green florescence intensity of the EGFP reporter, the SRIP-induced cytopathic effect, and ZIKV’s non-structural protein expression. Moreover, ZIKV Natal RGN SRIPs effectively self-replicated in rhabdomyosarcoma/muscle, glioblastoma/astrocytoma, and retinal pigmented epithelial cells, displaying unique cell susceptibility with differential attachment activity. Therefore, the recombinant ZIKV Natal RGN strain was rescued as SRIPs that could be used to elucidate the biological features of a neurotropic strain regarding cell tropism and pathogenic components, apply for antiviral agent screening, and develop vaccine candidates. Full article
(This article belongs to the Section Animal Viruses)
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