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Identification of candidate target genes for endometrial cancer, such as ANO1, using weighted gene co-expression
Fangzhen Wang1, Bo Wang2, Junbei Long3
1The Outpatient Office, Affiliated Hospital of Xiangyang Vocational and Technical College, Xiangyang, Hubei 441000, P.R. China.
Abstract:
Network-based systems biology has become an important method for analysis of high-throughput gene expression data and gene function mining. The aim of the present study was to implement a weighted gene co-expression network analysis to screen genes that were significantly correlated with the clinical phenotype of endometrial cancer based on data from The Cancer Genome Atlas. By using the function 'pickSoftThreshold' in R software, the optimum soft thresholding power was determined to be 4. Subsequently, a total of 2,414 expressed genes were identified among 19,791 genes from 506 samples, which were divided into 24 modules according to the different expression patterns. After analyzing the correlation between the gene expression in these 24 modules and the clinical phenotype of endometrial cancer, the anoctamin 1 (ANO1) gene was selected for further analysis. The Chi-squared test indicated that ANO1 was significantly associated with age (P=0.047), histological type (P<0.001), clinical stage (P<0.001), pathological grade (P<0.001) and positive peritoneal washing (P=0.001) of endometrial carcinoma. Kaplan-Meier survival analysis revealed that a high level of ANO1 was significantly associated with a good prognosis for endometrial cancer patients. Univariate and multivariate Cox regression analysis indicated that ANO1 is an independent prognostic factor in endometrial cancer. Further characterization of the most relevant module containing ANO1 with the database for annotation, visualization and integrated discovery tool suggested that ANO1 is involved in various pathways, including metabolic pathways. The present study suggests that ANO1 may be a potential marker for good prognosis in endometrial cancer.
Insights
Anoktamin 1 (ANO1) gene expression is linked to better outcomes in endometrial cancer. This study identified ANO1 as a potential biomarker for good prognosis in endometrial cancer patients.
Area of Science:
- Genomics
- Systems Biology
- Oncology
Background:
- Network-based systems biology is crucial for analyzing gene expression data and mining gene functions.
- Understanding gene expression patterns is key to identifying biomarkers for cancer prognosis.
Purpose of the Study:
- To implement weighted gene co-expression network analysis to identify genes correlated with endometrial cancer clinical phenotypes.
- To investigate the prognostic significance of the anoctamin 1 (ANO1) gene in endometrial cancer.
Main Methods:
- Weighted gene co-expression network analysis (WGCNA) was performed on The Cancer Genome Atlas (TCGA) endometrial cancer data.
- Gene expression data from 506 samples were clustered into 24 modules, and correlations with clinical phenotypes were assessed.
- Statistical analyses including Chi-squared tests, Kaplan-Meier survival analysis, and Cox regression were used to evaluate ANO1's significance.
Main Results:
- A total of 2,414 genes were identified and clustered into 24 modules.
- The anoctamin 1 (ANO1) gene showed significant associations with age, histological type, clinical stage, pathological grade, and peritoneal washing status.
- High ANO1 expression was correlated with a good prognosis and identified as an independent prognostic factor in endometrial cancer.
Conclusions:
- The anoctamin 1 (ANO1) gene is significantly associated with various clinical characteristics of endometrial cancer.
- ANO1 may serve as a valuable biomarker for predicting a good prognosis in endometrial cancer patients.
- Further research into ANO1's role in metabolic pathways could offer new therapeutic insights.
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