RETRACTED: The Transcription Factor Sterile Alpha Motif (SAM) Pointed Domain-containing ETS Transcription Factor (SPDEF) Is Required for E-cadherin Expression in Prostate Cancer Cells (Retracted Article)

被引:12
|
作者
Pal, Mintu [1 ]
Koul, Sweaty [1 ,3 ]
Koul, Hari K. [1 ,2 ,3 ]
机构
[1] Univ Colorado, Dept Surg, Sch Med, Program Urosci,Div Urol, Aurora, CO 80045 USA
[2] Univ Colorado, Ctr Comprehens Canc, Aurora, CO 80045 USA
[3] Denver Vet Adm Med Ctr, Denver, CO 80220 USA
基金
美国国家卫生研究院;
关键词
EPITHELIAL-MESENCHYMAL TRANSITION; BETA-CATENIN; AGGRESSIVE PHENOTYPE; ANOIKIS RESISTANCE; PROGNOSTIC VALUE; GENE-EXPRESSION; BREAST-CANCER; FACTOR SNAIL; FACTOR PDEF; TGF-BETA;
D O I
10.1074/jbc.M112.434225
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
Loss of E-cadherin is one of the key steps in tumor progression. Our previous studies demonstrate that SAM pointed domain-containing ETS transcription factor (SPDEF) inhibited prostate cancer metastasis in vitro and in vivo. In the present study, we evaluated the relationship between SPDEF and E-cadherin expression in an effort to better understand the mechanism of action of SPDEF in prostate tumor cell invasion and metastasis. The results presented here demonstrate a direct correlation between expression of E-cadherin and SPDEF in prostate cancer cells. Additional data demonstrate that modulation of E-cadherin and SPDEF had similar effects on cell migration/invasion. In addition, siRNA-mediated knockdown of E-cadherin was sufficient to block the effects of SPDEF on cell migration and invasion. We also show that stable forced expression of SPDEF results in increased expression of E-cadherin, whereas down-regulation of SPDEF decreased E-cadherin expression. In addition, we demonstrate that SPDEF expression is not regulated by E-cadherin. Moreover, our chromatin immunoprecipitation and luciferase reporter assay revealed that SPDEF occupies E-cadherin promoter site and acts as a direct transcriptional inducer of E-cadherin in prostate cancer cells. Taken together, to the best of our knowledge, these studies are the first demonstrating requirement of SPDEF for expression of E-cadherin, an essential epithelial cell junction protein. Given that loss of E-cadherin is a central tenant in tumor metastasis, the results of our studies, by providing a new mechanism for regulation of E-cadherin expression, could have far reaching impact.
引用
收藏
页码:12222 / 12231
页数:10
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