PAX6 Is Expressed in Pancreatic Cancer and Actively Participates in Cancer Progression through Activation of the MET Tyrosine Kinase Receptor Gene

被引:45
|
作者
Mascarenhas, Joseph B. [1 ]
Young, Kacey P. [1 ]
Littlejohn, Erica L. [1 ]
Yoo, Brian K. [1 ]
Salgia, Ravi [1 ]
Lang, Deborah [1 ]
机构
[1] Univ Chicago, Dept Med, Chicago, IL 60637 USA
基金
美国国家卫生研究院;
关键词
HEPATOCYTE GROWTH-FACTOR; C-MET; PAIRED DOMAIN; UP-REGULATION; TRANSCRIPTIONAL ACTIVATION; GLIOBLASTOMA CELLS; INVASIVE GROWTH; IDENTIFICATION; PROTOONCOGENE; SUPPRESSES;
D O I
10.1074/jbc.M109.047209
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Tumors of the exocrine pancreas have a poor prognosis. Several proteins are overexpressed in this cancer type, including the MET tyrosine kinase receptor and the transcription factor PAX6. In this report, we find that PAX6(5a), an alternately spliced variant form of PAX6, is expressed in pancreatic carcinoma cell lines at higher levels than the canonical PAX6 protein. Both protein forms of PAX6 bind directly to an enhancer element in the MET promoter and activate the expression of the MET gene. In addition, inhibition of PAX6 transcripts leads to a decline in cell growth and survival, differentiation, and a concurrent reduction of MET protein expression. These data support a model for a neoplastic pathway, where expression of a transcription factor from development activates the MET receptor, a protein that has been directly linked to protumorigenic processes of resisting apoptosis, tumor growth, invasion, and metastasis.
引用
收藏
页码:27524 / 27532
页数:9
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