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ROBO3s: a novel ROBO3 short isoform promoting breast cancer aggressiveness.
Werner, Marcel; Dyas, Anna; Parfentev, Iwan; Schmidt, Geske E; Mieczkowska, Iga K; Müller-Kirschbaum, Lukas C; Müller, Claudia; Kalkhof, Stefan; Reinhardt, Oliver; Urlaub, Henning; Alves, Frauke; Gallwas, Julia; Prokakis, Evangelos; Wegwitz, Florian.
Afiliação
  • Werner M; Department of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, Göttingen, Germany.
  • Dyas A; Chromosome Dynamics and Genome Stability, Institute of Epigenetics and Stem Cells, Helmholtz Zentrum München, Munich, Germany.
  • Parfentev I; Department of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, Göttingen, Germany.
  • Schmidt GE; International Max-Planck Research School for Molecular Biology, Göttingen, Germany.
  • Mieczkowska IK; Early Cancer Institute, University of Cambridge, Department of Oncology, Hutchison Research Centre, Box 197 Cambridge Biomedical Campus, Cambridge, Germany.
  • Müller-Kirschbaum LC; Bioanalytical Mass Spectrometry group, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.
  • Müller C; Department of Gastroenterology, Gastrointestinal Oncology and Endocrinology, University Medical Center Göttingen, Göttingen, Germany.
  • Kalkhof S; Department of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, Göttingen, Germany.
  • Reinhardt O; Department of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, Göttingen, Germany.
  • Urlaub H; Department of Preclinical Development and Validation, Fraunhofer Institute for Cell Therapy and Immunology, Leipzig, Germany.
  • Alves F; Department of Preclinical Development and Validation, Fraunhofer Institute for Cell Therapy and Immunology, Leipzig, Germany.
  • Gallwas J; Translational Molecular Imaging, Max-Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.
  • Prokakis E; Bioanalytical Mass Spectrometry group, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.
  • Wegwitz F; Bioanalytics, Institute of Clinical Chemistry, University Medical Center Göttingen, Göttingen, Germany.
Cell Death Dis ; 13(9): 762, 2022 09 03.
Article em En | MEDLINE | ID: mdl-36057630
Basal-like breast cancer (BLBC) is a highly aggressive breast cancer subtype frequently associated with poor prognosis. Due to the scarcity of targeted treatment options, conventional cytotoxic chemotherapies frequently remain the standard of care. Unfortunately, their efficacy is limited as BLBC malignancies rapidly develop resistant phenotypes. Using transcriptomic and proteomic approaches in human and murine BLBC cells, we aimed to elucidate the molecular mechanisms underlying the acquisition of aggressive and chemotherapy-resistant phenotypes in these mammary tumors. Specifically, we identified and characterized a novel short isoform of Roundabout Guidance Receptor 3 (ROBO3s), upregulated in BLBC in response to chemotherapy and encoding for a protein variant lacking the transmembrane domain. We established an important role for the ROBO3s isoform, mediating cancer stem cell properties by stimulating the Hippo-YAP signaling pathway, and thus driving resistance of BLBC cells to cytotoxic drugs. By uncovering the conservation of ROBO3s expression across multiple cancer types, as well as its association with reduced BLBC-patient survival, we emphasize its potential as a prognostic marker and identify a novel attractive target for anti-cancer drug development.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Neoplasias Mamárias Animais / Antineoplásicos Tipo de estudo: Guideline Limite: Animals / Female / Humans Idioma: En Revista: Cell Death Dis Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Neoplasias Mamárias Animais / Antineoplásicos Tipo de estudo: Guideline Limite: Animals / Female / Humans Idioma: En Revista: Cell Death Dis Ano de publicação: 2022 Tipo de documento: Article