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10.18632/oncotarget.13396

http://scihub22266oqcxt.onion/10.18632/oncotarget.13396
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suck abstract from ncbi


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pmid27861149
      Oncotarget 2017 ; 8 (1 ): 354-363
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  • AAV-Mediated angiotensin 1-7 overexpression inhibits tumor growth of lung cancer in vitro and in vivo #MMPMID27861149
  • Chen X ; Chen S ; Pei N ; Mao Y ; Wang S ; Yan R ; Bai N ; Li A ; Zhang Y ; Du H ; Chen B ; Sumners C ; Li J ; Li H
  • Oncotarget 2017[Jan]; 8 (1 ): 354-363 PMID27861149 show ga
  • Ang-(1-7) inhibits lung cancer cell growth both in vitro and in vivo. However, the molecular mechanism of action is unclear and also the rapid degradation of Ang-(1-7) in vivo limits its clinical application. Here, we have demonstrated that Ang- (1-7) inhibits lung cancer cell growth by interrupting pre-replicative complex assembly and restrains epithelial-mesenchymal transition via Cdc6 inhibition. Furthermore, we constructed a mutant adeno-associated viral vector AAV8 (Y733F) that produced stable and high efficient Ang-(1-7) expression in a xenograft tumor model. The results show that AAV8-mediated Ang-(1-7) over-expression can remarkably suppress tumor growth in vivo by down-regulating Cdc6 and anti-angiogenesis. Ang-(1-7) over-expression via the AAV8 method may be a promising strategy for lung cancer treatment.
  • |Angiotensin I/genetics/*metabolism/therapeutic use [MESH]
  • |Animals [MESH]
  • |Carcinoma, Non-Small-Cell Lung/drug therapy/*pathology [MESH]
  • |Cell Cycle Proteins/*metabolism [MESH]
  • |Cell Line, Tumor [MESH]
  • |Cell Movement [MESH]
  • |Cell Proliferation [MESH]
  • |DNA Replication [MESH]
  • |Dependovirus/*genetics [MESH]
  • |Down-Regulation [MESH]
  • |Epithelial-Mesenchymal Transition [MESH]
  • |Female [MESH]
  • |Genetic Vectors/genetics [MESH]
  • |Humans [MESH]
  • |Immunohistochemistry [MESH]
  • |Lung Neoplasms/drug therapy/*pathology [MESH]
  • |Lung/blood supply/pathology [MESH]
  • |Mice [MESH]
  • |Mice, Inbred BALB C [MESH]
  • |Mice, Nude [MESH]
  • |Multienzyme Complexes/metabolism [MESH]
  • |Neovascularization, Pathologic/drug therapy/pathology [MESH]
  • |Nuclear Proteins/*metabolism [MESH]
  • |Peptide Fragments/genetics/*metabolism/therapeutic use [MESH]
  • |Proteolysis [MESH]
  • |Vascular Endothelial Growth Factor A/metabolism [MESH]


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