A Support Vector Machine Model Predicting the Risk of Duodenal Cancer in Patients with Familial Adenomatous Polyposis at the Transcript Levels.

Objective. Familial adenomatous polyposis (FAP) is one major type of inherited duodenal cancer. The estimate of duodenal cancer risk in patients with FAP is critical for selecting the optimal treatment strategy. Methods. Microarray datasets related with FAP were retrieved from the Gene Expression Om...

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Publicado en:BioMed Research International pp. 1 - 13
Autores principales: Liu, Weiqing, Dong, Jian, Ma, Shumin, Liang, Lei, Yang, Jun
Formato: pictorial research tables/charts Journal Article
Publicado: Wiley-Blackwell 6/16/2020
Acceso en línea:Ver este registro en EBSCOhost
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      dt: 6/16/2020
      pid: 480
      pub: Wiley-Blackwell
      place: Malden, Massachusetts
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        143804543
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        10.1155/2020/5807295
        143804543
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        atl: A Support Vector Machine Model Predicting the Risk of Duodenal Cancer in Patients with Familial Adenomatous Polyposis at the Transcript Levels.
      aug:
        au:
          Liu, Weiqing
          Dong, Jian
          Ma, Shumin
          Liang, Lei
          Yang, Jun
        affil: Department of Internal Medicine Oncology, First Affiliated Hospital of Kunming Medical University, Kunming, China
      sug:
        subj:
          Support Vector Machine
          Adenomatous Polyposis Coli Complications
          Duodenal Neoplasms Risk Factors
          Risk Assessment
          Gene Expression Profiling
          Human
          Microarray Analysis
          Comparative Studies
          Metabolic Networks and Pathways
          Intracellular Signaling Peptides and Proteins Analysis
          Cell Cycle Proteins Analysis
          Chemokines Analysis
          Transcription Factors Analysis
          Polymerase Chain Reaction Methods
      ab: Objective. Familial adenomatous polyposis (FAP) is one major type of inherited duodenal cancer. The estimate of duodenal cancer risk in patients with FAP is critical for selecting the optimal treatment strategy. Methods. Microarray datasets related with FAP were retrieved from the Gene Expression Omnibus (GEO) database. Differentially expressed genes were identified by FAP vs. normal samples and FAP and duodenal cancer vs. normal samples. Furthermore, functional enrichment analyses of these differentially expressed genes were performed. A support vector machine (SVM) was performed to train and validate cancer risk prediction model. Results. A total of 196 differentially expressed genes were identified between FAP compared with normal samples. 177 similarly expressed genes were identified both in FAP and duodenal cancer, which were mainly enriched in pathways in cancer and metabolic-related pathway, indicating that these genes in patients with FAP could contribute to duodenal cancer. Among them, Cyclin D1, SDF-1, AXIN, and TCF were significantly upregulated in FAP tissues using qRT-PCR. Based on the 177 genes, an SVM model was constructed for prediction of the risk of cancer in patients with FAP. After validation, the model can accurately distinguish FAP patients with high risk from those with low risk for duodenal cancer. Conclusion. This study proposed a cancer risk prediction model based on an SVM at the transcript levels.
      pubtype: Academic Journal
      doctype:
        pictorial
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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