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Aberrant epithelial polarity cues drive the development of precancerous airway lesions.
Tilston-Lunel, Andrew; Mazzilli, Sarah; Kingston, Nathan M; Szymaniak, Aleksander D; Hicks-Berthet, Julia; Kern, Joseph G; Abo, Kristine; Reid, Mary E; Perdomo, Catalina; Wilson, Andrew A; Spira, Avrum; Beane, Jennifer; Varelas, Xaralabos.
Afiliação
  • Tilston-Lunel A; Department of Biochemistry, Boston University School of Medicine, Boston, MA 02118.
  • Mazzilli S; Department of Medicine, Boston University School of Medicine, Boston, MA 02118.
  • Kingston NM; Department of Biochemistry, Boston University School of Medicine, Boston, MA 02118.
  • Szymaniak AD; Department of Biochemistry, Boston University School of Medicine, Boston, MA 02118.
  • Hicks-Berthet J; Department of Biochemistry, Boston University School of Medicine, Boston, MA 02118.
  • Kern JG; Department of Biochemistry, Boston University School of Medicine, Boston, MA 02118.
  • Abo K; Department of Medicine, Boston University School of Medicine, Boston, MA 02118.
  • Reid ME; Center for Regenerative Medicine of Boston University and Boston Medical Center, Boston, MA 02118.
  • Perdomo C; Department of Medicine, Roswell Park Comprehensive Cancer Center, Buffalo, NY 14203.
  • Wilson AA; Department of Medicine, Boston University School of Medicine, Boston, MA 02118.
  • Spira A; Department of Medicine, Boston University School of Medicine, Boston, MA 02118.
  • Beane J; Center for Regenerative Medicine of Boston University and Boston Medical Center, Boston, MA 02118.
  • Varelas X; Pulmonary Center, Boston University School of Medicine , Boston, MA 02118.
Proc Natl Acad Sci U S A ; 118(18)2021 05 04.
Article em En | MEDLINE | ID: mdl-33903236
ABSTRACT
Molecular events that drive the development of precancerous lesions in the bronchial epithelium, which are precursors of lung squamous cell carcinoma (LUSC), are poorly understood. We demonstrate that disruption of epithelial cellular polarity, via the conditional deletion of the apical determinant Crumbs3 (Crb3), initiates and sustains precancerous airway pathology. The loss of Crb3 in adult luminal airway epithelium promotes the uncontrolled activation of the transcriptional regulators YAP and TAZ, which stimulate intrinsic signals that promote epithelial cell plasticity and paracrine signals that induce basal-like cell growth. We show that aberrant polarity and YAP/TAZ-regulated gene expression associates with human bronchial precancer pathology and disease progression. Analyses of YAP/TAZ-regulated genes further identified the ERBB receptor ligand Neuregulin-1 (NRG1) as a key transcriptional target and therapeutic targeting of ERBB receptors as a means of preventing and treating precancerous cell growth. Our observations offer important molecular insight into the etiology of LUSC and provides directions for potential interception strategies of lung cancer.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Lesões Pré-Cancerosas / Glicoproteínas de Membrana / Carcinoma de Células Escamosas / Neuregulina-1 / Proteínas de Sinalização YAP / Neoplasias Pulmonares Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Lesões Pré-Cancerosas / Glicoproteínas de Membrana / Carcinoma de Células Escamosas / Neuregulina-1 / Proteínas de Sinalização YAP / Neoplasias Pulmonares Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article