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Modeling human brain tumors in flies, worms, and zebrafish: From proof of principle to novel therapeutic targets.
Shahzad, Uswa; Taccone, Michael S; Kumar, Sachin A; Okura, Hidehiro; Krumholtz, Stacey; Ishida, Joji; Mine, Coco; Gouveia, Kyle; Edgar, Julia; Smith, Christian; Hayes, Madeline; Huang, Xi; Derry, W Brent; Taylor, Michael D; Rutka, James T.
Afiliação
  • Shahzad U; Institute of Medical Science, Faculty of Medicine, University of Toronto, Toronto, Canada.
  • Taccone MS; Arthur and Sonia Labatt Brain Tumor Research Center, Hospital for Sick Children, Toronto, Canada.
  • Kumar SA; Arthur and Sonia Labatt Brain Tumor Research Center, Hospital for Sick Children, Toronto, Canada.
  • Okura H; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Canada.
  • Krumholtz S; Arthur and Sonia Labatt Brain Tumor Research Center, Hospital for Sick Children, Toronto, Canada.
  • Ishida J; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Canada.
  • Mine C; Arthur and Sonia Labatt Brain Tumor Research Center, Hospital for Sick Children, Toronto, Canada.
  • Gouveia K; Arthur and Sonia Labatt Brain Tumor Research Center, Hospital for Sick Children, Toronto, Canada.
  • Edgar J; Arthur and Sonia Labatt Brain Tumor Research Center, Hospital for Sick Children, Toronto, Canada.
  • Smith C; Arthur and Sonia Labatt Brain Tumor Research Center, Hospital for Sick Children, Toronto, Canada.
  • Hayes M; Arthur and Sonia Labatt Brain Tumor Research Center, Hospital for Sick Children, Toronto, Canada.
  • Huang X; Arthur and Sonia Labatt Brain Tumor Research Center, Hospital for Sick Children, Toronto, Canada.
  • Derry WB; Arthur and Sonia Labatt Brain Tumor Research Center, Hospital for Sick Children, Toronto, Canada.
  • Taylor MD; Developmental and Stem Cell Biology, Hospital for Sick Children, Toronto, Canada.
  • Rutka JT; Arthur and Sonia Labatt Brain Tumor Research Center, Hospital for Sick Children, Toronto, Canada.
Neuro Oncol ; 23(5): 718-731, 2021 05 05.
Article em En | MEDLINE | ID: mdl-33378446
For decades, cell biologists and cancer researchers have taken advantage of non-murine species to increase our understanding of the molecular processes that drive normal cell and tissue development, and when perturbed, cause cancer. The advent of whole-genome sequencing has revealed the high genetic homology of these organisms to humans. Seminal studies in non-murine organisms such as Drosophila melanogaster, Caenorhabditis elegans, and Danio rerio identified many of the signaling pathways involved in cancer. Studies in these organisms offer distinct advantages over mammalian cell or murine systems. Compared to murine models, these three species have shorter lifespans, are less resource intense, and are amenable to high-throughput drug and RNA interference screening to test a myriad of promising drugs against novel targets. In this review, we introduce species-specific breeding strategies, highlight the advantages of modeling brain tumors in each non-mammalian species, and underscore the successes attributed to scientific investigation using these models. We conclude with an optimistic proposal that discoveries in the fields of cancer research, and in particular neuro-oncology, may be expedited using these powerful screening tools and strategies.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Peixe-Zebra / Neoplasias Encefálicas Limite: Animals / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Peixe-Zebra / Neoplasias Encefálicas Limite: Animals / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article