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10.18632/oncotarget.11722

http://scihub22266oqcxt.onion/10.18632/oncotarget.11722
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C5356564!5356564 !27588393
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suck abstract from ncbi


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pmid27588393
      Oncotarget 2016 ; 7 (42 ): 68397-68411
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  • MicroRNA-140-5p targets insulin like growth factor 2 mRNA binding protein 1 (IGF2BP1) to suppress cervical cancer growth and metastasis #MMPMID27588393
  • Su Y ; Xiong J ; Hu J ; Wei X ; Zhang X ; Rao L
  • Oncotarget 2016[Oct]; 7 (42 ): 68397-68411 PMID27588393 show ga
  • MicroRNAs (miRNAs) are a class of small non-coding RNA molecules that play important roles in carcinogenesis and tumor progression. Previous studies have revealed that MicroRNA-140-5p (miR-140-5p) was abnormally expressed in several cancers. However, its function and possible mechanism in cervical cancer (CC) remains unknown. In this study, the data mining results showed that miR-140-5p was down-regulated in CC specimens and the down-regulation of miR-140-5p was associated with CC poor prognosis. These observations prompted us to further investigate the roles and mechanisms of miR-140-5p in human CC pathogenesis. We found that the over-expression/inhibition of miR-140-5p significantly decreased/increased cell proliferation, migration, and invasion in CC cells in vitro. Meanwhile, the results from in vivo assays showed that the over-expression of miR-140-5p induced significantly suppression of tumor growth and metastasis in nude mice. Furthermore, Insulin like growth factor 2 mRNA binding protein 1 (IGF2BP1) was identified as a direct target of miR-140-5p, and both gain-of-function and loss-of-function assays revealed that IGF2BP1 is also a functional target of miR-140-5p. Taken together, our findings suggested a novel miR-140-5p-IGF2BP1 regulatory circuit for CC pathogenesis, and miR-140-5p may be a potential target for CC therapy.
  • |*Gene Expression Regulation, Neoplastic [MESH]
  • |3' Untranslated Regions/genetics [MESH]
  • |Animals [MESH]
  • |Cell Line, Tumor [MESH]
  • |Cell Movement/genetics [MESH]
  • |Cell Proliferation/*genetics [MESH]
  • |Female [MESH]
  • |HeLa Cells [MESH]
  • |Humans [MESH]
  • |Mice, Inbred BALB C [MESH]
  • |Mice, Nude [MESH]
  • |MicroRNAs/*genetics [MESH]
  • |Neoplasm Metastasis [MESH]
  • |RNA Interference [MESH]
  • |RNA-Binding Proteins/*genetics/metabolism [MESH]
  • |Transplantation, Heterologous [MESH]


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