Identification of Biomarkers for Esophageal Squamous Cell Carcinoma Using Feature Selection and Decision Tree Methods

Author:

Tung Chun-Wei12,Wu Ming-Tsang345,Chen Yu-Kuei6,Wu Chun-Chieh7,Chen Wei-Chung8,Li Hsien-Pin89,Chou Shah-Hwa9,Wu Deng-Chyang1011,Wu I-Chen1011

Affiliation:

1. School of Pharmacy, Kaohsiung Medical University, Kaohsiung 80708, Taiwan

2. Ph.D. Program in Toxicology, Kaohsiung Medical University, Kaohsiung 80708, Taiwan

3. Department of Family Medicine, Kaohsiung Medical University Hospital, Kaohsiung 80708, Taiwan

4. Department of Public Health, Kaohsiung Medical University, Kaohsiung 80708, Taiwan

5. Center of Environmental and Occupational Medicine, Kaohsiung Municipal Hsiao-Kang Hospital, Kaohsiung 812, Taiwan

6. Department of Food Science and Nutrition, Meiho University, Pingtung 91202, Taiwan

7. Department of Pathology, Kaohsiung Medical University Hospital, Kaohsiung 80708, Taiwan

8. Division of Chest Surgery, Kaohsiung Municipal Hsiao-Kang Hospital, Kaohsiung 812, Taiwan

9. Division of Chest Surgery, Department of Surgery, Kaohsiung Medical University Hospital, Kaohsiung 80708, Taiwan

10. Division of Gastroenterology, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung 80708, Taiwan

11. Department of Medicine, Faculty of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung 80708, Taiwan

Abstract

Esophageal squamous cell cancer (ESCC) is one of the most common fatal human cancers. The identification of biomarkers for early detection could be a promising strategy to decrease mortality. Previous studies utilized microarray techniques to identify more than one hundred genes; however, it is desirable to identify a small set of biomarkers for clinical use. This study proposes a sequential forward feature selection algorithm to design decision tree models for discriminating ESCC from normal tissues. Two potential biomarkers of RUVBL1 and CNIH were identified and validated based on two public available microarray datasets. To test the discrimination ability of the two biomarkers, 17 pairs of expression profiles of ESCC and normal tissues from Taiwanese male patients were measured by using microarray techniques. The classification accuracies of the two biomarkers in all three datasets were higher than 90%. Interpretable decision tree models were constructed to analyze expression patterns of the two biomarkers. RUVBL1 was consistently overexpressed in all three datasets, although we found inconsistent CNIH expression possibly affected by the diverse major risk factors for ESCC across different areas.

Funder

National Science Council

Publisher

Hindawi Limited

Subject

General Environmental Science,General Biochemistry, Genetics and Molecular Biology,General Medicine

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