Upregulation of focal adhesion kinase (FAK) expression in ductal carcinoma in situ (DCIS) is an early event in breast tumorigenesis

Harry M. Lightfoot, Amy Lark, Chad A. Livasy, Dominic T. Moore, David Cowan, Lynn Dressler, Rolf J. Craven, William G. Cance

Research output: Contribution to journalArticlepeer-review

88 Scopus citations


Focal adhesion kinase (FAK) is a protein tyrosine kinase that is overexpressed in a subset of invasive breast cancers. FAK transmits signals that mediate several functions including tumor cell proliferation, migration, adhesion and survival. We used immunohistochemical techniques to assess FAK expression in patients with fibrocystic disease (FCD), atypical ductal hyperplasia (ADH), ductal carcinoma in situ (DCIS) and infiltrating ductal carcinoma (IDC). Formalin-fixed, paraffin-embedded (FFPE) tissue sections were obtained from 119 patients (12 FCD, 38 ADH, 51 DCIS and 18 IDC). The anti-FAK 4.47 monoclonal antibody was used to detect FAK expression. FAK expression was scored as high (3 or 4 intensity and ≥90 positive cells) or low. The DCIS tissue sections demonstrated high FAK expression in 34/51 (66) of the sections. High FAK expression was demonstrated in 6/18 (33) of the IDC tissue sections and 8/38 (21)of the ADH tissue sections. None (0/12) of the FCD tissues sections stained high for FAK. The pattern of FAK expression in DCIS was significantly higher than ADH (p < 0.0001) and IDC (p =0.02). We conclude that FAK overexpression in preinvasive, DCIS tumors precedes tumor cell invasion or metastasis, suggesting that FAK may function as a survival signal and be an early event in breast tumorigenesis.

Original languageEnglish
Pages (from-to)109-116
Number of pages8
JournalBreast Cancer Research and Treatment
Issue number2
StatePublished - Nov 2004

Bibliographical note

Funding Information:
This study was supported in part by CA65910 and CA83895 from the National Cancer Institute, Bethesda, MD, USA.


  • breast cancer
  • focal adhesion kinase
  • immunohistochemistry
  • protein tyrosine kinases

ASJC Scopus subject areas

  • Oncology
  • Cancer Research


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