Silencing of Eag1 Gene Inhibits Osteosarcoma Proliferation and Migration by Targeting STAT3-VEGF Pathway.

So far, the role of Ether à go-go 1 (Eag1) potassium channels in migration and invasion progression of cancers remains elusive. In the present study, the effects of Eag1 knockdown on osteosarcoma cell proliferation, growth, and apoptosis were examined.Then, we evaluated the effects of Eag1 silencing...

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Publicado en:BioMed Research International Vol. 2015; pp. 1 - 11
Autores principales: Xinyu Wu, Zhida Chen, Wengrong Zeng, Yuanfu Zhong, Qingjun Liu, Jin Wu
Formato: pictorial research tables/charts Journal Article
Publicado: Wiley-Blackwell 12/9/2015
Acceso en línea:Ver este registro en EBSCOhost
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      dt: 12/9/2015
      vid: 2015
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      pub: Wiley-Blackwell
      place: Malden, Massachusetts
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        10.1155/2015/617316
        114127858
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        atl: Silencing of Eag1 Gene Inhibits Osteosarcoma Proliferation and Migration by Targeting STAT3-VEGF Pathway.
      aug:
        au:
          Xinyu Wu
          Zhida Chen
          Wengrong Zeng
          Yuanfu Zhong
          Qingjun Liu
          Jin Wu
        affil: Department of Neurology, The Affiliated Southeast Hospital of Xiamen University, Zhangzhou 363000, China.
      sug:
        subj:
          Osteosarcoma
          Cell Migration Inhibition
          Cell Proliferation
          Genetics
          Vascular Endothelial Growth Factors Physiology
          Carrier Proteins Physiology
          Human
          Neoplasm Invasiveness
          Apoptosis
      ab: So far, the role of Ether à go-go 1 (Eag1) potassium channels in migration and invasion progression of cancers remains elusive. In the present study, the effects of Eag1 knockdown on osteosarcoma cell proliferation, growth, and apoptosis were examined.Then, we evaluated the effects of Eag1 silencing on osteosarcoma cell migration and invasion. In addition, we detected the expression of vascular endothelial growth factor (VEGF) and signal transducer and activator of transcription 3 (STAT3) in osteosarcoma cell treated with Eag1 small interfering RNAs (siRNAs). Finally, STAT3 siRNA was employed to determine the influence of downregulation of STAT3 on cell proliferation and migration. The results showed that knockdown of Eag1 significantly suppressed osteosarcoma cell proliferation and osteosarcoma xenografts growth. However, Eag1 silencing had little effect on cell apoptosis. Additionally, osteosarcomacell adhesion, migration, and invasionwere also potently attenuated.Notably, the expression levels ofVEGFdecreased evidently upon Eag1 siRNAs treatment, paralleled with reductions in the expression levels of STAT3. Moreover, a similar pattern was observed in osteosarcoma cell proliferation and migration suppression between STAT3 siRNA and Eag1 siRNAs groups. Our data indicated that Eag1 promotes osteosarcoma proliferation and migration, at least in part, by targeting STAT3-VEGF pathway.
      pubtype: Academic Journal
      doctype:
        pictorial
        research
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      ougenre: Article
    language: English
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