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Integrative analysis of non-small cell lung cancer patient-derived xenografts identifies distinct proteotypes associated with patient outcomes.
Mirhadi, Shideh; Tam, Shirley; Li, Quan; Moghal, Nadeem; Pham, Nhu-An; Tong, Jiefei; Golbourn, Brian J; Krieger, Jonathan R; Taylor, Paul; Li, Ming; Weiss, Jessica; Martins-Filho, Sebastiao N; Raghavan, Vibha; Mamatjan, Yasin; Khan, Aafaque A; Cabanero, Michael; Sakashita, Shingo; Huo, Kugeng; Agnihotri, Sameer; Ishizawa, Kota; Waddell, Thomas K; Zadeh, Gelareh; Yasufuku, Kazuhiro; Liu, Geoffrey; Shepherd, Frances A; Moran, Michael F; Tsao, Ming-Sound.
Afiliação
  • Mirhadi S; Program in Cell Biology, Hospital for Sick Children, Toronto, ON, Canada.
  • Tam S; Department of Molecular Genetics, University of Toronto, Toronto, ON, Canada.
  • Li Q; Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
  • Moghal N; Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
  • Pham NA; Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
  • Tong J; Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
  • Golbourn BJ; Program in Cell Biology, Hospital for Sick Children, Toronto, ON, Canada.
  • Krieger JR; John G. Rangos Sr. Research Center, Children's Hospital of Pittsburgh, and Department of Neurological Surgery, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
  • Taylor P; SPARC BioCentre, Hospital for Sick Children, Toronto, ON, Canada.
  • Li M; Program in Cell Biology, Hospital for Sick Children, Toronto, ON, Canada.
  • Weiss J; Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
  • Martins-Filho SN; Department of Biostatistics, Princess Margaret Cancer Centre, Toronto, ON, Canada.
  • Raghavan V; Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
  • Mamatjan Y; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada.
  • Khan AA; Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
  • Cabanero M; Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
  • Sakashita S; Program in Cell Biology, Hospital for Sick Children, Toronto, ON, Canada.
  • Huo K; Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
  • Agnihotri S; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada.
  • Ishizawa K; Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
  • Waddell TK; Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
  • Zadeh G; John G. Rangos Sr. Research Center, Children's Hospital of Pittsburgh, and Department of Neurological Surgery, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
  • Yasufuku K; Division of Thoracic Surgery, Toronto General Hospital, University Health Network, Toronto, ON, Canada.
  • Liu G; Division of Thoracic Surgery, Toronto General Hospital, University Health Network, Toronto, ON, Canada.
  • Shepherd FA; Department of Surgery, University of Toronto, Toronto, ON, Canada.
  • Moran MF; Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
  • Tsao MS; Department of Surgery, University of Toronto, Toronto, ON, Canada.
Nat Commun ; 13(1): 1811, 2022 04 05.
Article em En | MEDLINE | ID: mdl-35383171
ABSTRACT
Non-small cell lung cancer (NSCLC) is the leading cause of cancer deaths worldwide. Only a fraction of NSCLC harbor actionable driver mutations and there is an urgent need for patient-derived model systems that will enable the development of new targeted therapies. NSCLC and other cancers display profound proteome remodeling compared to normal tissue that is not predicted by DNA or RNA analyses. Here, we generate 137 NSCLC patient-derived xenografts (PDXs) that recapitulate the histology and molecular features of primary NSCLC. Proteome analysis of the PDX models reveals 3 adenocarcinoma and 2 squamous cell carcinoma proteotypes that are associated with different patient outcomes, protein-phosphotyrosine profiles, signatures of activated pathways and candidate targets, and in adenocarcinoma, stromal immune features. These findings portend proteome-based NSCLC classification and treatment and support the PDX resource as a viable model for the development of new targeted therapies.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Animals / Humans Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Animals / Humans Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Canadá