TY - JOUR
T1 - LEF1 targeting EMT in prostate cancer invasion is regulated by miR-34a
AU - Liang, Jiaqian
AU - Li, Yirong
AU - Daniels, Garrett
AU - Sfanos, Karen
AU - De Marzo, Angelo
AU - Wei, Jianjun
AU - Li, Xin
AU - Chen, Wenqiang
AU - Wang, Jinhua
AU - Zhong, Xuelin
AU - Melamed, Jonathan
AU - Zhao, Jun
AU - Lee, Peng
N1 - Publisher Copyright:
© 2015 American Association for Cancer Research.
PY - 2015/4/1
Y1 - 2015/4/1
N2 - The microRNA-34a (miR-34a), a tumor-suppressive microRNA (miRNA), is implicated in epithelial-mesenchymal transition (EMT) and cancer stem cells. Lymphoid enhancer-binding factor-1 (LEF1) is a key transcription factor in the Wnt signaling pathway, and has been suggested to be involved in regulation of cell proliferation and invasion. Here, the molecular mechanism of miR-34a and LEF1 in cooperatively regulating prostate cancer cell invasion is described. Molecular profiling analysis of miRNA levels in prostate cancer cells revealed a negative correlation between miR-34a and LEF1 expression, and the downregulation of LEF1 by miR-34a was confirmed by luciferase assays. Furthermore, miR-34a specifically repressed LEF1 expression through direct binding to its 30-untranslated regions (30-UTR). miR-34a modulated the levels of LEF1 to regulate EMT in prostate cancer cells. Functionally, miR-34a negatively correlated with the migration and invasion of prostate cancer cells through LEF1. An analysis of miR-34a expression levels in matched human tumor and benign tissues demonstrated consistent and statistically significant downregulation of miR-34a in primary prostate cancer specimens. These data strongly suggest that miR-34a/LEF1 regulation ofEMTplays an important role in prostate cancer migration and invasion.
AB - The microRNA-34a (miR-34a), a tumor-suppressive microRNA (miRNA), is implicated in epithelial-mesenchymal transition (EMT) and cancer stem cells. Lymphoid enhancer-binding factor-1 (LEF1) is a key transcription factor in the Wnt signaling pathway, and has been suggested to be involved in regulation of cell proliferation and invasion. Here, the molecular mechanism of miR-34a and LEF1 in cooperatively regulating prostate cancer cell invasion is described. Molecular profiling analysis of miRNA levels in prostate cancer cells revealed a negative correlation between miR-34a and LEF1 expression, and the downregulation of LEF1 by miR-34a was confirmed by luciferase assays. Furthermore, miR-34a specifically repressed LEF1 expression through direct binding to its 30-untranslated regions (30-UTR). miR-34a modulated the levels of LEF1 to regulate EMT in prostate cancer cells. Functionally, miR-34a negatively correlated with the migration and invasion of prostate cancer cells through LEF1. An analysis of miR-34a expression levels in matched human tumor and benign tissues demonstrated consistent and statistically significant downregulation of miR-34a in primary prostate cancer specimens. These data strongly suggest that miR-34a/LEF1 regulation ofEMTplays an important role in prostate cancer migration and invasion.
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U2 - 10.1158/1541-7786.MCR-14-0503
DO - 10.1158/1541-7786.MCR-14-0503
M3 - Article
C2 - 25587085
AN - SCOPUS:84928040874
SN - 1541-7786
VL - 13
SP - 681
EP - 688
JO - Molecular Cancer Research
JF - Molecular Cancer Research
IS - 4
ER -