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2016 ; 7
(52
): 86134-86147
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Gli1 promotes colorectal cancer metastasis in a Foxm1-dependent manner by
activating EMT and PI3K-AKT signaling
#MMPMID27863385
Zhang C
; Wang Y
; Feng Y
; Zhang Y
; Ji B
; Wang S
; Sun Y
; Zhu C
; Zhang D
; Sun Y
Oncotarget
2016[Dec]; 7
(52
): 86134-86147
PMID27863385
show ga
Colorectal cancer(CRC) is one of the most commonly diagnosed cancers in human
beings and metastasis is the main death reason. Recently, Gli1 has been reported
to be a key regulator of various cancer biologies and genes expressions. However,
the detailed molecular mechanism of Gli1 in CRC metastasis remains largely
unknown. In this study, we aimed to investigate the role of Gli1 in CRC
metastasis. We used qRT-PCR, Immunohistochemistry and Western blot to test the
expression levels of Gli1, Foxm1 and other target genes in the tissues and cells;
Lentivirus stable transfection to change the expression levels of Gli1 and Foxm1;
Wound-healing, cell invasion, migration assays and tail vein metastatic assay to
test the role of Gli1 in CRC metastasis in vitro and vivo. We demonstrated that
Gli1 was significantly overexpressed in colorectal cancer tissues and cells.
Foxm1 level had a positive correlation with Gli1. Furthermore, we found that Gli1
promotes colorectal cancer cells metastasis in a Foxm1-dependent manner by
activating EMT and PI3K-AKT signaling. Thus, we proved that Gli1 plays important
role in CRC metastasis and provided a new visual field on the therapy of CRC
metastasis.