Pancreatic cancer biomarker detection by two support vector strategies for recursive feature elimination

Biomark Med. 2019 Feb;13(2):105-121. doi: 10.2217/bmm-2018-0273. Epub 2019 Feb 15.

Abstract

Aim: Pancreatic cancer is one of the worst malignant tumors in prognosis. Therefore, to reduce the mortality rate of pancreatic cancer, early diagnosis and prompt treatment are particularly important.

Results: We put forward a new feature-selection method that was used to find clinical markers for pancreatic cancer by combination of Support Vector Machine Recursive Feature Elimination (SVM-RFE) and Large Margin Distribution Machine Recursive Feature Elimination (LDM-RFE) algorithms. As a result, seven differentially expressed genes were predicted as specific biomarkers for pancreatic cancer because of their highest accuracy of classification on cancer and normal samples.

Conclusion: Three (MMP7, FOS and A2M) out of the seven predicted gene markers were found to encode proteins secreted into urine, providing potential diagnostic evidences for pancreatic cancer.

Keywords: LDM-RFE; SVM-RFE; biomarker detection; pancreatic cancer; urinary excretory protein.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Algorithms*
  • Biomarkers, Tumor / genetics*
  • Biomarkers, Tumor / urine
  • Case-Control Studies
  • Gene Expression Profiling*
  • Humans
  • Matrix Metalloproteinase 7 / genetics
  • Matrix Metalloproteinase 7 / urine
  • Pancreas / metabolism
  • Pancreas / pathology*
  • Pancreatic Neoplasms / diagnosis*
  • Pancreatic Neoplasms / genetics
  • Pancreatic Neoplasms / urine
  • Prognosis
  • Proto-Oncogene Proteins c-fos / genetics
  • Proto-Oncogene Proteins c-fos / urine
  • Support Vector Machine*
  • Survival Rate
  • alpha-Macroglobulins / genetics
  • alpha-Macroglobulins / urine

Substances

  • A2M protein, human
  • Biomarkers, Tumor
  • FOS protein, human
  • Proto-Oncogene Proteins c-fos
  • alpha-Macroglobulins
  • MMP7 protein, human
  • Matrix Metalloproteinase 7