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10.18632/oncotarget.14529

http://scihub22266oqcxt.onion/10.18632/oncotarget.14529
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C5355270!5355270!28076327
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suck abstract from ncbi


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pmid28076327      Oncotarget 2017 ; 8 (7): 11356-71
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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): 11356-71 PMID28076327show 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.
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