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Hippo Pathway in Cancer: Aberrant Regulation and Therapeutic Opportunities.
Calses, Philamer C; Crawford, James J; Lill, Jennie R; Dey, Anwesha.
Afiliación
  • Calses PC; Department of Discovery Oncology, Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, USA; Department of Microchemistry, Proteomics, and Lipidomics, Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, USA.
  • Crawford JJ; Department of Discovery Chemistry, Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, USA.
  • Lill JR; Department of Microchemistry, Proteomics, and Lipidomics, Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, USA.
  • Dey A; Department of Discovery Oncology, Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, USA. Electronic address: dey.anwesha@gene.com.
Trends Cancer ; 5(5): 297-307, 2019 05.
Article en En | MEDLINE | ID: mdl-31174842
ABSTRACT
The Hippo pathway remains a central focus in both basic and translational research and is a key modulator of developmental biology. Dysregulation of the pathway is associated with a plethora of human cancers and there are multiple efforts to target key components of the pathway for disease intervention. In this review, we briefly highlight the latest research advances around the core components of the Hippo pathway in cancer. More specifically, we discuss several genetic aberrations of these factors as mechanisms for the development of cancers, including genetic amplification, deletion, and gene fusions. Additionally, we highlight the role of the Hippo pathway in cancer therapy resistance and tumor immunogenicity. Last, we summarize the ongoing efforts to target the pathway in cancers.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Transducción de Señal / Proteínas Serina-Treonina Quinasas / Neoplasias Tipo de estudio: Etiology_studies Límite: Humans Idioma: En Revista: Trends Cancer Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Transducción de Señal / Proteínas Serina-Treonina Quinasas / Neoplasias Tipo de estudio: Etiology_studies Límite: Humans Idioma: En Revista: Trends Cancer Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos