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AAV-Mediated angiotensin 1-7 overexpression inhibits tumor growth of lung cancer in vitro and in vivo.
- Source :
-
Oncotarget [Oncotarget] 2017 Jan 03; Vol. 8 (1), pp. 354-363. - Publication Year :
- 2017
-
Abstract
- 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.
- Subjects :
- Angiotensin I genetics
Angiotensin I therapeutic use
Animals
Carcinoma, Non-Small-Cell Lung drug therapy
Cell Line, Tumor
Cell Movement
Cell Proliferation
DNA Replication
Down-Regulation
Epithelial-Mesenchymal Transition
Female
Genetic Vectors genetics
Humans
Immunohistochemistry
Lung blood supply
Lung pathology
Lung Neoplasms drug therapy
Mice
Mice, Inbred BALB C
Mice, Nude
Multienzyme Complexes metabolism
Neovascularization, Pathologic drug therapy
Neovascularization, Pathologic pathology
Peptide Fragments genetics
Peptide Fragments therapeutic use
Proteolysis
Vascular Endothelial Growth Factor A metabolism
Xenograft Model Antitumor Assays
Angiotensin I metabolism
Carcinoma, Non-Small-Cell Lung pathology
Cell Cycle Proteins metabolism
Dependovirus genetics
Lung Neoplasms pathology
Nuclear Proteins metabolism
Peptide Fragments metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1949-2553
- Volume :
- 8
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Oncotarget
- Publication Type :
- Academic Journal
- Accession number :
- 27861149
- Full Text :
- https://doi.org/10.18632/oncotarget.13396