p53 regulates FAK expression in human tumor cells

• Published in: Molecular carcinogenesis Vol. 47; no. 5; pp. 373 - 382
• Main Authors: Golubovskaya, Vita M., Finch, Richard, Kweh, Frederick, Massoll, Nicole A., Campbell-Thompson, Martha, Wallace, Margaret R., Cance, William G.
• Format: Journal Article
• Language: English
• Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 01-05-2008
• Subjects: Adenoviridae - genetics; Animals; Base Sequence; Blotting, Western; breast cancer; Breast Neoplasms - genetics; Breast Neoplasms - metabolism; Breast Neoplasms - pathology; Cells, Cultured; Chromatin Immunoprecipitation; colon cancer; Colonic Neoplasms - genetics; Colonic Neoplasms - metabolism; Colonic Neoplasms - pathology; Cyclin-Dependent Kinase Inhibitor p21 - metabolism; Fibroblasts - cytology; Fibroblasts - metabolism; Fluorouracil - pharmacology; focal adhesion kinase; Focal Adhesion Protein-Tyrosine Kinases - genetics; Focal Adhesion Protein-Tyrosine Kinases - metabolism; Gene Expression Regulation, Enzymologic - physiology; Humans; Immunoenzyme Techniques; Loss of Heterozygosity; Luciferases - metabolism; Mice; Mice, Knockout; Molecular Sequence Data; Mutation - genetics; p53; Polymorphism, Single-Stranded Conformational; Promoter Regions, Genetic - genetics; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger - genetics; RNA, Messenger - metabolism; Transcription, Genetic; Transcriptional Activation; Transfection; tumor; Tumor Suppressor Protein p53 - physiology
• ISSN: 0899-1987; 1098-2744
• DOI: 10.1002/mc.20395

Attenuation of the p53 protein is one of the most common abnormalities in human tumors. Another important marker of tumorigenesis is focal adhesion kinase (FAK), a 125‐kDa tyrosine kinase that is overexpressed at the mRNA and protein levels in a variety of human tumors. FAK is a critical regulator of adhesion, motility, metastasis, and survival signaling. We have characterized the FAK promoter and demonstrated that p53 can inhibit the FAK promoter activity in vitro. In the present study, we showed that p53 can bind the FAK promoter‐chromatin region in vivo by chromatin immunoprecipitation (ChIP) assay. Furthermore, we demonstrated down‐regulation of FAK mRNA and protein levels by adenoviral overexpression of p53. We introduced plasmids with different mutations in the DNA‐binding domain of p53 (R175H, p53 R248W and R273H) into HCTp53−/− cells and showed that these mutations of p53 did not bind FAK promoter and did not inhibit FAK promoter activity, unlike wild type p53. We analyzed primary breast and colon cancers for p53 mutations and FAK expression, and showed that FAK expression was increased in tumors containing mutations of p53 compared to tumors with wild type p53. In addition, tumor‐derived missense mutations in the DNA‐binding domain (R282, R249, and V173) also led to increased FAK promoter activity. Thus, the present data show that p53 can regulate FAK expression during tumorigenesis. © 2007 Wiley‐Liss, Inc.