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Published on: April 7, 2017
Snail promotes epithelial-mesenchymal transition and invasiveness in human ovarian cancer cells
Yu-Lou Wang1, Xue-Min Zhao1, Zhi-Feng Shuai2
1Department of General Surgery, The First Affiliated Hospital of Qiqihar Medical University Qiqihar 161042, Heilongjiang, China.
Abstract:
There are limited reports with respect to the study on the epithelium-mesenchymal transformation (EMT) mediated by Snail in the ovarian cancer. This study detected the expression of Snail and related EMT markers in the ovarian cancer tissues, and explored the possible molecular mechanism of EMT mediated by Snail in the metastasis of ovarian cancer. The patients diagnosed with ovarian cancer according to the pathology were recruited in this study during 2010-2014. The carcinoma tissue and normal tissue adjacent to carcinoma were surgically obtained from patients. The genes of E-cadherin, β-catenin, Fibronectin and N-cadherin were detected using the RT-PCR. The 64 patients were recruited and diagnosed as ovarian cancer by pathological examination. The expression levels of Snail, Fibronectin and N-cadherin in the stage III and IV were higher than those in the stage I and II, respectively (all P < 0.05). However, the expression levels of E-cadherin and β-catenin decreased along with the stage developed (trend test, both P < 0.05), respectively. The expression of Snail was positively correlated with the expression of Fibronectin, N-cadherin, but negatively correlated with the expression of E-cadherin and β-catenin. The number of A2780 cells entering into the lower compartment in the group of carcinoma tissue were significantly higher than that in the group of normal tissue after transfected with Snail expression vector. While, the invasion ability of A2780 significantly reduced after RNAi-Snail. The correlation between Snail and invasion and metastasis of ovarian cancer and epithelial-mesenchymal transition based on tissue and cell levels, and to some extent explored the molecular mechanism of the EMT process mediated by Snail.
Insights
Snail protein drives epithelial-mesenchymal transition (EMT) in ovarian cancer, promoting metastasis. Inhibiting Snail reduces cancer cell invasion, highlighting its role in ovarian cancer progression.
Area of Science:
- Oncology
- Molecular Biology
- Cell Biology
Background:
- Epithelial-mesenchymal transition (EMT) is crucial for cancer metastasis.
- The role of Snail in mediating EMT in ovarian cancer requires further investigation.
Purpose of the Study:
- To investigate Snail expression and its association with EMT markers in ovarian cancer.
- To explore the molecular mechanisms of Snail-mediated EMT in ovarian cancer metastasis.
Main Methods:
- Retrospective analysis of 64 ovarian cancer patients' tissues (2010-2014).
- RT-PCR to detect E-cadherin, β-catenin, Fibronectin, and N-cadherin gene expression.
- In vitro cell invasion assays using A2780 cells with Snail overexpression and RNAi.
Main Results:
- Snail, Fibronectin, and N-cadherin expression increased with advanced ovarian cancer stages (III/IV vs. I/II).
- E-cadherin and β-catenin expression decreased in advanced stages.
- Snail expression positively correlated with Fibronectin and N-cadherin, and negatively with E-cadherin and β-catenin.
- Snail overexpression enhanced A2780 cell invasion; RNAi-Snail reduced it.
Conclusions:
- Snail is significantly associated with EMT and advanced stages in ovarian cancer.
- Snail plays a critical role in promoting ovarian cancer cell invasion and metastasis.
- Targeting Snail may offer a therapeutic strategy for ovarian cancer.
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