Survivin Is a Novel Target of CD44-Promoted Breast Tumor Invasion

被引:33
作者
Abdraboh, Mohamed E. [1 ,2 ,3 ]
Gaur, Rajiv L. [1 ]
Hollenbach, Andrew D. [4 ]
Sandquist, Dane [3 ]
Raj, Madhwa H. G. [5 ]
Ouhtit, Allal [1 ]
机构
[1] Sultan Qaboos Univ, Coll Med & Hlth Sci, Dept Genet, Muscat, Oman
[2] Mansoura Univ, Fac Sci, Dept Zool, Mansoura 35516, Egypt
[3] Louisiana State Univ, Dept Pathol, Hlth Sci Ctr, New Orleans, LA USA
[4] Louisiana State Univ, Dept Genet, Hlth Sci Ctr, New Orleans, LA USA
[5] Louisiana State Univ, Hlth Sci Ctr, Dept Obstet & Gynecol, New Orleans, LA USA
关键词
CANCER-CELLS; GENE-EXPRESSION; CD44; GROWTH; RECEPTOR; TRANSCRIPTION; SUPPRESSION; METASTASIS; HYALURONAN; RESISTANCE;
D O I
10.1016/j.ajpath.2011.04.042
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The hyaluronan (HA) receptor CD44 plays an essential role in cell-cell or cell-extraccllular matrix communications and is a bioactive signal transmitter. Although a number of studies have described the function of CD44 in breast cancer (BC) metastasis, the underlying mechanisms have yet to be determined. By using a validated tetracycline-off-regulated CD44 expression system in the MCF-7 cell line combined with microarray analysis, we identified survivin (SVV) as a potential downstream transcriptional target of CD44. To test the hypothesis that SW underpins CD44-promoted BC cell invasion, we combined molecular and pharmacologic approaches and showed that CD44 induction increased SW expression levels, which in turn promotes BC cell invasion. Further, clinical analysis of breast tissue samples showed that SVV expression patterns paralleled those of the standard form of CD44 during breast tumor progression. More interestingly, we identified the PI3K/E2F1 pathway as a potential molecular link between HA/CD44 activation and SVV transcription. In addition to identifying SW as a target for HA/CD44 signaling, this investigation provides a better understanding of the molecular mechanisms that underpin the novel function of SVV in breast cancer metastasis. (Am J Pathol 2011, 179:555-563; DOI: 10.1016/j.ajpath.2011.04.042)
引用
收藏
页码:555 / 563
页数:9
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