학술논문

A protein network map of head and neck cancer reveals PIK3CA mutant drug sensitivity
Document Type
article
Source
Science. 374(6563)
Subject
Biochemistry and Cell Biology
Biomedical and Clinical Sciences
Oncology and Carcinogenesis
Biological Sciences
Cancer
Genetics
Rare Diseases
Dental/Oral and Craniofacial Disease
2.1 Biological and endogenous factors
Aetiology
Animals
Carcinoma
Squamous Cell
Cell Line
Tumor
Cell Movement
Class I Phosphatidylinositol 3-Kinases
Drug Resistance
Neoplasm
Female
Head and Neck Neoplasms
Humans
Intracellular Signaling Peptides and Proteins
Mice
Mice
Nude
Microfilament Proteins
Mutation
Protein Interaction Maps
Receptor
Fibroblast Growth Factor
Type 3
Xenograft Model Antitumor Assays
General Science & Technology
Language
Abstract
We outline a framework for elucidating tumor genetic complexity through multidimensional protein-protein interaction maps and apply it to enhancing our understanding of head and neck squamous cell carcinoma. This network uncovers 771 interactions from cancer and noncancerous cell states, including WT and mutant protein isoforms. Prioritization of cancer-enriched interactions reveals a previously unidentified association of the fibroblast growth factor receptor tyrosine kinase 3 with Daple, a guanine-nucleotide exchange factor, resulting in activation of Gαi- and p21-activated protein kinase 1/2 to promote cancer cell migration. Additionally, we observe mutation-enriched interactions between the human epidermal growth factor receptor 3 (HER3) receptor tyrosine kinase and PIK3CA (the alpha catalytic subunit of phosphatidylinositol 3-kinase) that can inform the response to HER3 inhibition in vivo. We anticipate that the application of this framework will be valuable for translating genetic alterations into a molecular and clinical understanding of the underlying biology of many disease areas.