ΔNp63 isoforms regulate CD44 and keratins 4, 6, 14 and 19 in squamous cell carcinoma of head and neck

被引:58
作者
Boldrup, L.
Coates, P. J.
Gu, X.
Nylander, K.
机构
[1] Umea Univ, Dept Med Biosci Pathol, SE-90185 Umea, Sweden
[2] Univ Dundee, Ninewells Hosp & Med Sch, Div Pathol & Neurosci, Dundee DD1 9SY, Scotland
关键词
p63; CD44; stem cells; keratins; adhesion; differentiation;
D O I
10.1002/path.2237
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The human p63 gene codes for multiple protein isoforms and is commonly over-expressed in squamous cell carcinoma of head and neck (SCCHN). This expression is predominantly of the Delta N- and beta-isoforms, the former lacking the p53-related transactivation domain. p63 can activate or repress transcription of p53 and p73 target genes, but also has unique transcriptional targets and, unlike other p53 family members, is required for normal development and differentiation of squarnous epithelia. We have identified novel targets of p63, using microarray analysis of SCCHN cells that stably over-express individual Delta Np63 isoforms. All three isofornis induced expression of the cancer stem cell marker, CD44, with the Delta Np63 beta isoform showing strongest induction. Using chromatin immunoprecipitation, we were unable to show direct binding of p63 to the CD44 promoter, but found that p63 specifically increased expression of CD44 lacking variant exon 2. Each of the Delta Np63 isoforms up-regulated expression of keratins 6A and 14 and down-regulated expression of keratins 4 and 19, in keeping with their expression patterns in SCCHN. The data strengthen the idea that p63 has key roles in regulating normal and abnormal differentiation processes through both induction and repression of genes with opposite functions. The identification of up-regulation and differential splicing of CD44 following p63 over-expression indicates roles in the regulation of adhesion, metastasis and the cancer stem cell phenotype. Copyrigt (c) 2007 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
引用
收藏
页码:384 / 391
页数:8
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