4.7 Article

Using aptamers to elucidate esophageal cancer clinical samples

Journal

SCIENTIFIC REPORTS
Volume 5, Issue -, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/srep18516

Keywords

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Funding

  1. National Natural Science Foundation of China [NSFC 81370983, NSFC 21221003, NSFC 21327009]
  2. Foundation of National Key Scientific Instrument and Equipment Development Projects [2011YQ0301241403]
  3. National Key Scientific Program of China [2011CB911000]
  4. National Natural Science Youth Foundation of China [81400864, 81500692]
  5. Hunan Province Natural Science Key Fund Project [2014SK2003]
  6. Foundation of China Hunan Provincial Science & Technology Department [2014FJ3109]
  7. Scientific Research Project of Hunan Provincial Health Department [B2013-010]
  8. Collaborative Innovation Center for Chemistry and Molecular Medicine [80106001]
  9. Special Fund for Young Teachers of Central South University [2012QNZT100]
  10. NSFC [NSFC 21221003, NSFC 21327009]
  11. China National Instrumentation Program [2011YQ03012412]
  12. National Institutes of Health [GM079359, GM 111386, CA133086]
  13. Pathology Department of Xiangya Hospital

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The epithelial cell adhesion molecule (EpCAM) is closely correlated with the occurrence and development of various cancers of epithelial origin. This study tested, for the first time, the ability of EpCAM aptamer SYL3C to detect EpCAM expression in 170 cases of esophageal cancer (EC) and precancerous lesions, as well as 20 cases of EC series samples, using immunofluorescence imaging analysis. Corresponding antibodies were used as control. EpCAM overexpression was 98% in both esophageal squamous cell carcinoma (ESCC) and esophageal adenocarcinoma (EACA) and 100% in metastasis, but no EpCAM overexpression was detected in undifferentiated EC (UEC). Significant differences were noted among various stages of differentiation (p < 0.05) with the degree of differentiation inversely correlated with the expression of EpCAM. Overexpressed EpCAM was detected in severe dysplasia, but negative in mild to moderate dysplasia and benign esophageal lesions. In a competitive binding experiment, EpCAM aptamer generated a staining pattern similar to that of antibody, but the binding sites with EpCAM were different. Based on these results, it can be concluded that EpCAM is suitable for use as an EC biomarker, therapeutic target, and effective parameter for tumor transfer and prognosis evaluation by aptamer SYL3C staining.

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