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A conditional inducible JAK2V617F transgenic mouse model reveals myeloproliferative disease that is reversible upon switching off transgene expression.
Chapeau, Emilie A; Mandon, Emeline; Gill, Jason; Romanet, Vincent; Ebel, Nicolas; Powajbo, Violetta; Andraos-Rey, Rita; Qian, Zhiyan; Kininis, Miltos; Zumstein-Mecker, Sabine; Ito, Moriko; Hynes, Nancy E; Tiedt, Ralph; Hofmann, Francesco; Eshkind, Leonid; Bockamp, Ernesto; Kinzel, Bernd; Mueller, Matthias; Murakami, Masato; Baffert, Fabienne; Radimerski, Thomas.
Afiliación
  • Chapeau EA; Disease Area Oncology, Novartis Institutes for BioMedical Research, Basel, Switzerland.
  • Mandon E; Disease Area Oncology, Novartis Institutes for BioMedical Research, Basel, Switzerland.
  • Gill J; Friedrich Miescher Institute for Biomedical Research, Basel, Switzerland.
  • Romanet V; Disease Area Oncology, Novartis Institutes for BioMedical Research, Basel, Switzerland.
  • Ebel N; Disease Area Oncology, Novartis Institutes for BioMedical Research, Basel, Switzerland.
  • Powajbo V; Disease Area Oncology, Novartis Institutes for BioMedical Research, Basel, Switzerland.
  • Andraos-Rey R; Disease Area Oncology, Novartis Institutes for BioMedical Research, Basel, Switzerland.
  • Qian Z; Disease Area Oncology, Novartis Institutes for BioMedical Research, Basel, Switzerland.
  • Kininis M; Disease Area Oncology, Novartis Institutes for BioMedical Research, Basel, Switzerland.
  • Zumstein-Mecker S; Disease Area Oncology, Novartis Institutes for BioMedical Research, Basel, Switzerland.
  • Ito M; Disease Area Oncology, Novartis Institutes for BioMedical Research, Basel, Switzerland.
  • Hynes NE; Friedrich Miescher Institute for Biomedical Research, Basel, Switzerland.
  • Tiedt R; Disease Area Oncology, Novartis Institutes for BioMedical Research, Basel, Switzerland.
  • Hofmann F; Disease Area Oncology, Novartis Institutes for BioMedical Research, Basel, Switzerland.
  • Eshkind L; Institute for Translational Immunology and Research Center for Immunotherapy, University Medical Center, Johannes Gutenberg University, Mainz, Germany.
  • Bockamp E; Institute for Translational Immunology and Research Center for Immunotherapy, University Medical Center, Johannes Gutenberg University, Mainz, Germany.
  • Kinzel B; Chemical Biology and Therapeutics, Novartis Institutes for BioMedical Research, Basel, Switzerland.
  • Mueller M; Chemical Biology and Therapeutics, Novartis Institutes for BioMedical Research, Basel, Switzerland.
  • Murakami M; Disease Area Oncology, Novartis Institutes for BioMedical Research, Basel, Switzerland.
  • Baffert F; Disease Area Oncology, Novartis Institutes for BioMedical Research, Basel, Switzerland.
  • Radimerski T; Disease Area Oncology, Novartis Institutes for BioMedical Research, Basel, Switzerland.
PLoS One ; 14(10): e0221635, 2019.
Article en En | MEDLINE | ID: mdl-31600213
Aberrant activation of the JAK/STAT pathway is thought to be the critical event in the pathogenesis of the chronic myeloproliferative neoplasms, polycythemia vera, essential thrombocythemia and primary myelofibrosis. The most frequent genetic alteration in these pathologies is the activating JAK2V617F mutation, and expression of the mutant gene in mouse models was shown to cause a phenotype resembling the human diseases. Given the body of genetic evidence, it has come as a sobering finding that JAK inhibitor therapy only modestly suppresses the JAK2V617F allele burden, despite showing clear benefits in terms of reducing splenomegaly and constitutional symptoms in patients. To gain a better understanding if JAK2V617F is required for maintenance of myeloproliferative disease once it has evolved, we generated a conditional inducible transgenic JAK2V617F mouse model using the SCL-tTA-2S tet-off system. Our model corroborates that expression of JAK2V617F in hematopoietic stem and progenitor cells recapitulates key hallmarks of human myeloproliferative neoplasms, and exhibits gender differences in disease manifestation. The disease was found to be transplantable, and importantly, reversible when transgenic JAK2V617F expression was switched off. Our results indicate that mutant JAK2V617F-specific inhibitors should result in profound disease modification by disabling the myeloproliferative clone bearing mutant JAK2.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Células Madre Hematopoyéticas / Regulación de la Expresión Génica / Transgenes / Janus Quinasa 2 / Trastornos Mieloproliferativos Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2019 Tipo del documento: Article País de afiliación: Suiza Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Células Madre Hematopoyéticas / Regulación de la Expresión Génica / Transgenes / Janus Quinasa 2 / Trastornos Mieloproliferativos Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2019 Tipo del documento: Article País de afiliación: Suiza Pais de publicación: Estados Unidos