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2017 ; 8
(7
): 11356-11371
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gab.com Text
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MiR-410 induces stemness by inhibiting Gsk3? but upregulating ?-catenin in
non-small cells lung cancer
#MMPMID28076327
Ke X
; Yuan Y
; Guo C
; Yang Y
; Pu Q
; Hu X
; Tang K
; Luo X
; Jiang Q
; Su X
; Liu L
; Zhu W
; Wei Y
Oncotarget
2017[Feb]; 8
(7
): 11356-11371
PMID28076327
show ga
Our previous research indicated miR-410 played a critical role in promoting the
tumorigenesis and development of NSCLC (non-small cells lung cancer). MiR-410 has
been recently reported to be crucial for development and differentiation of
embryonic stem cells. But it remains elusive whether miR-410 stimulates the
stemness of cancer until now. Herein, we identify miR-410 induces the stemness
and is associated with the progression of NSCLC. We demonstrate miR-410 increases
the levels of stem cells marker Sox2, Oct4, Nanog, CXCR4 as well as lung cancer
stem cells surface marker CD44 and CD166. MiR-410 promotes stem cells-like
properties such as proliferation, sphere formation, metastasis and
chemoresistance. Moreover, Gsk3? is directly targeted and post-transcriptionally
downregulated by miR-410. Also, the expression levels of miR-410 and Gsk3? may be
correlated to clinicopathological differentiation in NSCLC tumor specimens.
Additionally, we demonstrate miR-410 induces stemness through inhibiting Gsk3?
but increasing Sox2, Oct4, Nanog and CXCR4, which binds to ?-catenin signaling.
In conclusion, our findings identify the miR-410/Gsk3?/?-catenin signaling axis
is a novel molecular circuit in inducing stemness of NSCLC.