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ΔNp63γ/SRC/Slug Signaling Axis Promotes Epithelial-to-Mesenchymal Transition in Squamous Cancers.
Srivastava, Kirtiman; Pickard, Adam; Craig, Stephanie G; Quinn, Gerard P; Lambe, Shauna M; James, Jacqueline A; McDade, Simon S; McCance, Dennis J.
Affiliation
  • Srivastava K; Centre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, United Kingdom. k.srivastava@qub.ac.uk s.mcdade@qub.ac.uk dmccance@salud.unm.edu.
  • Pickard A; Centre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, United Kingdom.
  • Craig SG; The Wellcome Trust Centre for Cell Matrix Research, University of Manchester, Manchester, United Kingdom.
  • Quinn GP; Centre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, United Kingdom.
  • Lambe SM; Centre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, United Kingdom.
  • James JA; Centre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, United Kingdom.
  • McDade SS; Centre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, United Kingdom.
  • McCance DJ; Centre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, United Kingdom. k.srivastava@qub.ac.uk s.mcdade@qub.ac.uk dmccance@salud.unm.edu.
Clin Cancer Res ; 24(16): 3917-3927, 2018 08 15.
Article in En | MEDLINE | ID: mdl-29739791
ABSTRACT

Purpose:

To investigate the regulation of epithelial-to-mesenchymal transition (EMT) in head and neck squamous cell carcinoma (HNSCC) and its importance in tumor invasion.Experimental

Design:

We use a three-dimensional invasive organotypic raft culture model of human foreskin keratinocytes expressing the E6/E7 genes of the human papilloma virus-16, coupled with bioinformatic and IHC analysis of patient samples to investigate the role played by EMT in invasion and identify effectors and upstream regulatory pathways.

Results:

We identify SNAI2 (Slug) as a critical effector of EMT-activated downstream of TP63 overexpression in HNSCC. Splice-form-specific depletion and rescue experiments further identify the ΔNp63γ isoform as both necessary and sufficient to activate the SRC signaling axis and SNAI2-mediated EMT and invasion. Moreover, elevated SRC levels are associated with poor outcome in patients with HNSCC in The Cancer Genome Atlas dataset. Importantly, the effects on EMT and invasions and SNAI2 expression can be reversed by genetic or pharmacologic inhibition of SRC.

Conclusions:

Overexpression of ΔNp63γ modulates cell invasion by inducing targetable SRC-Slug-evoked EMT in HNSCC, which can be reversed by inhibitors of the SRC signaling. Clin Cancer Res; 24(16); 3917-27. ©2018 AACR.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Transcription Factors / Src-Family Kinases / Tumor Suppressor Proteins / Snail Family Transcription Factors / Squamous Cell Carcinoma of Head and Neck Type of study: Prognostic_studies Limits: Humans Language: En Journal: Clin Cancer Res Journal subject: NEOPLASIAS Year: 2018 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Transcription Factors / Src-Family Kinases / Tumor Suppressor Proteins / Snail Family Transcription Factors / Squamous Cell Carcinoma of Head and Neck Type of study: Prognostic_studies Limits: Humans Language: En Journal: Clin Cancer Res Journal subject: NEOPLASIAS Year: 2018 Document type: Article