TY - JOUR
T1 - Aberrant overexpression of the cell polarity module Scribble in human cancer
AU - Vaira, Valentina
AU - Faversani, Alice
AU - Dohi, Takehiko
AU - Maggioni, Marco
AU - Nosotti, Mario
AU - Tosi, Delfina
AU - Altieri, Dario C.
AU - Bosari, Silvano
N1 - Funding Information:
Supported by a fellowship of the Doctorate School of Molecular Medicine at Università degli Studi di Milano (A.F.) and in part by grants from the National Institutes of Health ( CA140043 , CA78810 , and CA118005 to D.C.A.) and the Fondazione Berlucchi (S.B.).
PY - 2011/6
Y1 - 2011/6
N2 - Human Scribble (Scrib) is an evolutionary-conserved cell polarity protein, but its potential role in human cancer is controversial. Herein, we show that Scrib is nearly universally overexpressed in cultured tumor cell lines and genetically disparate cancer patient series compared with matched normal tissues in vivo. Instead of a membrane association seen in normal epithelia, tumor-associated Scrib is mislocalized and found predominantly in the cytosol. Small-interfering RNA silencing of Scrib in model lung adenocarcinoma A549 cells inhibited cell migration in wound-healing assays, suppressed tumor cell invasion across Matrigelcoated inserts, and down-regulated the expression of cell motility markers and mediators of epithelial-mesenchymal transition. These data uncover a previously unrecognized exploitation of Scrib for aberrant tumor cell motility and invasion, thus potentially contributing to disease progression in humans.
AB - Human Scribble (Scrib) is an evolutionary-conserved cell polarity protein, but its potential role in human cancer is controversial. Herein, we show that Scrib is nearly universally overexpressed in cultured tumor cell lines and genetically disparate cancer patient series compared with matched normal tissues in vivo. Instead of a membrane association seen in normal epithelia, tumor-associated Scrib is mislocalized and found predominantly in the cytosol. Small-interfering RNA silencing of Scrib in model lung adenocarcinoma A549 cells inhibited cell migration in wound-healing assays, suppressed tumor cell invasion across Matrigelcoated inserts, and down-regulated the expression of cell motility markers and mediators of epithelial-mesenchymal transition. These data uncover a previously unrecognized exploitation of Scrib for aberrant tumor cell motility and invasion, thus potentially contributing to disease progression in humans.
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U2 - 10.1016/j.ajpath.2011.02.028
DO - 10.1016/j.ajpath.2011.02.028
M3 - Article
C2 - 21549346
AN - SCOPUS:79959378518
SN - 0002-9440
VL - 178
SP - 2478
EP - 2483
JO - American Journal of Pathology
JF - American Journal of Pathology
IS - 6
ER -