Increased Expression of LYNX1 in Ovarian Serous Cystadenocarcinoma Predicts Poor Prognosis.

Few studies have reported the function of LYNX1 in ovarian cancer. We retrieved LYNX1 gene expression data and clinical information of 376 patients with ovarian cancer from The Cancer Genome Atlas (TCGA) project website. Wilcoxon signed-rank test and logistic regression were used to analyze the rela...

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Publicado en:BioMed Research International pp. 1 - 12
Autores principales: Liu, Hui, Wang, Ao, Ma, Yushan
Formato: research tables/charts Journal Article
Publicado: Wiley-Blackwell 11/25/2020
Acceso en línea:Ver este registro en EBSCOhost
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      dt: 11/25/2020
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      pub: Wiley-Blackwell
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        10.1155/2020/1392674
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        atl: Increased Expression of LYNX1 in Ovarian Serous Cystadenocarcinoma Predicts Poor Prognosis.
      aug:
        au:
          Liu, Hui
          Wang, Ao
          Ma, Yushan
        affil: Department of Anesthesiology, West China Second Hospital of Sichuan University, Key Laboratory of Birth Defects and Related Diseases of Women and Children, Sichuan University, Ministry of Education, Chengdu, China
      sug:
        subj:
          Ovarian Neoplasms Prognosis
          Neoplasms, Cystic, Mucinous, and Serous
          Adenocarcinoma Prognosis
          Gene Expression Profiling
          Proteins Metabolism
          Human
          Wilcoxon Signed Rank Test
          Logistic Regression
          Kaplan-Meier Estimator
          Univariate Statistics
          Biological Markers
          Genetic Techniques
      ab: Few studies have reported the function of LYNX1 in ovarian cancer. We retrieved LYNX1 gene expression data and clinical information of 376 patients with ovarian cancer from The Cancer Genome Atlas (TCGA) project website. Wilcoxon signed-rank test and logistic regression were used to analyze the relationship between clinical pathologic features and LYNX1 expression. The Kaplan–Meier method was used to draw survival curves of patients, and Cox regression was used to calculate the relationship between LYNX1 expression and survival rate or the clinicopathological characteristics of the patients. Gene set enrichment analysis (GSEA) was performed, and the correlation between LYNX1 expression and cancer immune infiltrates was investigated via single sample gene set enrichment analysis (ssGSEA). High LYNX1 expression in ovarian serous cystadenocarcinoma (OVs) was associated with tumor residual disease (RD). In Kaplan–Meier survival analysis, patients with OVs who also displayed high LYNX1 expression had decreased overall survival (OS) and disease-specific survival (DSS) than those with low LYNX1 expression. Univariate analysis also supported that patients with high LYNX1 expression had lower OS than those with low LYNX1 expression. LYNX1 expression has the potential to be a prognostic molecular marker of poor survival in OVs.
      pubtype: Academic Journal
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    language: English
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