Transcription factor Snai1-1 induces osteosarcoma invasion and metastasis by inhibiting E-cadherin expression
Author(s) -
Huiguang Yang,
Yunqing Zhang,
Zhengming Zhou,
Xuefeng Jiang,
Aidong Shen
Publication year - 2014
Publication title -
oncology letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.766
H-Index - 54
eISSN - 1792-1082
pISSN - 1792-1074
DOI - 10.3892/ol.2014.2079
Subject(s) - snai1 , small hairpin rna , osteosarcoma , transfection , epithelial–mesenchymal transition , cancer research , oncogene , metastasis , cadherin , transcription factor , biology , cell , cell cycle , cancer , cell culture , gene , gene knockdown , biochemistry , genetics
Osteosarcoma (OS) is a type of primary malignant bone tumor with a high propensity for local recurrence and distant metastasis. A previous study showed Snail-1 is highly expressed in OS cells. The present study aimed to investigate the association between the transcription factor Snai1 and E-cadherin in OS. SaOS 2 OS cells were transfected either with a plasmid expressing short hairpin RNA (shRNA) specific for the Snai1-1 gene (SaOS 2 -shRNA) or a negative control plasmid (SaOS 2 -Mock). The expression levels of E-cadherin and Snai1-1 in the transfected and control cells were determined by quantitative polymerase chain reaction and western blot analysis. In addition, the study was extended to evaluate the migratory and invasive properties of the cells through a Transwell experiment. The results show that E-cadherin was expressed at a high level in the SaOS 2 -shRNA cells, which were much less migratory and invasive than the control cells. Overexpression of Snai1-1 in OS is associated with tumor progression, possibly through the suppression of E-cadherin expression and induction of the process of epithelial-mesenchymal transition, which contributes to the proceeding invasion and metastasis of OS cells.
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