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JAK-STAT core cancer pathway: An integrative cancer interactome analysis.
Erdogan, Fettah; Radu, Tudor Bogdan; Orlova, Anna; Qadree, Abdul Khawazak; de Araujo, Elvin Dominic; Israelian, Johan; Valent, Peter; Mustjoki, Satu M; Herling, Marco; Moriggl, Richard; Gunning, Patrick Thomas.
Affiliation
  • Erdogan F; Department of Chemical and Physical Sciences, University of Toronto Mississauga, Mississauga, Ontario, Canada.
  • Radu TB; Department of Chemistry, University of Toronto, Toronto, Ontario, Canada.
  • Orlova A; Department of Chemical and Physical Sciences, University of Toronto Mississauga, Mississauga, Ontario, Canada.
  • Qadree AK; Department of Chemistry, University of Toronto, Toronto, Ontario, Canada.
  • de Araujo ED; Institute of Animal Breeding and Genetics, University of Veterinary Medicine, Vienna, Austria.
  • Israelian J; Department of Chemical and Physical Sciences, University of Toronto Mississauga, Mississauga, Ontario, Canada.
  • Valent P; Department of Chemistry, University of Toronto, Toronto, Ontario, Canada.
  • Mustjoki SM; Department of Chemical and Physical Sciences, University of Toronto Mississauga, Mississauga, Ontario, Canada.
  • Herling M; Department of Chemical and Physical Sciences, University of Toronto Mississauga, Mississauga, Ontario, Canada.
  • Moriggl R; Department of Chemistry, University of Toronto, Toronto, Ontario, Canada.
  • Gunning PT; Division of Hematology and Hemostaseology, Department of Internal Medicine I, Medical University of Vienna, Vienna, Austria.
J Cell Mol Med ; 26(7): 2049-2062, 2022 04.
Article de En | MEDLINE | ID: mdl-35229974
ABSTRACT
Through a comprehensive review and in silico analysis of reported data on STAT-linked diseases, we analysed the communication pathways and interactome of the seven STATs in major cancer categories and proposed rational targeting approaches for therapeutic intervention to disrupt critical pathways and addictions to hyperactive JAK/STAT in neoplastic states. Although all STATs follow a similar molecular activation pathway, STAT1, STAT2, STAT4 and STAT6 exert specific biological profiles associated with a more restricted pattern of activation by cytokines. STAT3 and STAT5A as well as STAT5B have pleiotropic roles in the body and can act as critical oncogenes that promote many processes involved in cancer development. STAT1, STAT3 and STAT5 also possess tumour suppressive action in certain mutational and cancer type context. Here, we demonstrated member-specific STAT activity in major cancer types. Through systems biology approaches, we found surprising roles for EGFR family members, sex steroid hormone receptor ESR1 interplay with oncogenic STAT function and proposed new drug targeting approaches of oncogenic STAT pathway addiction.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Facteurs de transcription STAT / Tumeurs Limites: Humans Langue: En Journal: J Cell Mol Med Sujet du journal: BIOLOGIA MOLECULAR Année: 2022 Type de document: Article Pays d'affiliation: Canada

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Facteurs de transcription STAT / Tumeurs Limites: Humans Langue: En Journal: J Cell Mol Med Sujet du journal: BIOLOGIA MOLECULAR Année: 2022 Type de document: Article Pays d'affiliation: Canada