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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 ): 11356-11371
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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.
  • |Adult [MESH]
  • |Aged [MESH]
  • |Animals [MESH]
  • |Blotting, Western [MESH]
  • |Carcinoma, Non-Small-Cell Lung/genetics/*pathology [MESH]
  • |Cell Line, Tumor [MESH]
  • |Female [MESH]
  • |Fluorescent Antibody Technique [MESH]
  • |Gene Expression Regulation, Neoplastic/*genetics [MESH]
  • |Glycogen Synthase Kinase 3 beta/*biosynthesis/genetics [MESH]
  • |Heterografts [MESH]
  • |Humans [MESH]
  • |Immunohistochemistry [MESH]
  • |Lung Neoplasms/genetics/*pathology [MESH]
  • |Male [MESH]
  • |Mice [MESH]
  • |Mice, Inbred BALB C [MESH]
  • |MicroRNAs/*genetics/metabolism [MESH]
  • |Middle Aged [MESH]
  • |Neoplastic Stem Cells/metabolism/pathology [MESH]
  • |Real-Time Polymerase Chain Reaction [MESH]
  • |Signal Transduction/physiology [MESH]
  • |Up-Regulation [MESH]


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