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2016 ; 9
(ä): 5417-25
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Long noncoding RNA SPRY4-IT1 promotes malignant development of colorectal cancer
by targeting epithelial-mesenchymal transition
#MMPMID27621655
Cao D
; Ding Q
; Yu W
; Gao M
; Wang Y
Onco Targets Ther
2016[]; 9
(ä): 5417-25
PMID27621655
show ga
The clinical significance and biological functions of long noncoding RNA SPRY4
intronic transcript 1 (SPRY4-IT1) in colorectal cancer (CRC) remain largely
unclear. Herein, we are the first to report that the SPRY4-IT1 was significantly
upregulated in CRC tissues, serum, and cells. Higher SPRY4-IT1 expression was
markedly associated with advanced Tumor Node Metastasis (TNM) stage in a cohort
of 84 CRC patients. Multivariate analyses indicated that SPRY4-IT1 expression
could be useful as an independent predictor for overall survival. Further in
vitro experiments revealed that knockdown of SPRY4-IT1 inhibited the
proliferation, migration, and invasion of CRC cells and induced cell cycle
arrestment. Moreover, we confirmed that the expression of epithelial-mesenchymal
transition-related genes was modulated through alteration of SPRY4-IT1
expression. These results suggest that SPRY4-IT1, as an oncogenic regulator, may
serve as a candidate prognostic marker and potential target for CRC therapies.