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Updated: May 18, 2026

A Lectin HPLC Method to Enrich Selectively-glycosylated Peptides from Complex Biological Samples
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A Lectin HPLC Method to Enrich Selectively-glycosylated Peptides from Complex Biological Samples

Published on: October 1, 2009

Glycan profiling of endometrial cancers using lectin microarray.

Yoshihiro Nishijima1, Masashi Toyoda, Mayu Yamazaki-Inoue

  • 1Department of Reproductive Biology, National Research Institute for Child Health and Development, 2-10-1 Okura, Tokyo 157-8535, Japan.

Genes to Cells : Devoted to Molecular & Cellular Mechanisms
|September 11, 2012
PubMed
Summary

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Lectin microarray analysis successfully distinguished endometrial cancer from normal tissue and differentiated cancer subtypes. This glycan profiling method shows potential for tumor characterization and predicting chemotherapy response.

Area of Science:

  • Glycobiology
  • Cancer Research
  • Biotechnology

Background:

  • Cell surface glycans undergo alterations during malignant transformation.
  • Distinguishing between normal endometrium and endometrial cancer is crucial for diagnosis and treatment.

Purpose of the Study:

  • To characterize and differentiate endometrial cancer from normal endometrium using glycan profiling.
  • To investigate the potential of lectin microarray analysis for tumor characterization and predicting chemotherapy response.

Main Methods:

  • Glycan profiling was performed using lectin microarray analysis on three cell lines (two endometrial cancer types and one normal endometrium).
  • Analysis involved 45 lectins to categorize cell lines and identify specific glycan differences between cancer subtypes (G1 and G3).

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  • Lectin microarray analysis was also applied to G3 type tissues and ovarian cancer cell lines.
  • Main Results:

    • The lectin microarray successfully categorized the three cell lines into distinct groups.
    • Six lectins (Ulex europaeus agglutinin I, Sambucus sieboldiana agglutinin, Sambucus nigra agglutinin, Trichosanthes japonica agglutinin I, Amaranthus caudatus agglutinin, and Bauhinia purpurea lectin) identified clear glycan differences between G1 and G3 endometrial cancer types.
    • Stage I and Stage III/IV G3 endometrial cancer tissues were distinguished by the signal patterns of Dolichos biflorus agglutinin, Bauhinia purpurea lectin, and Amaranthus caudatus agglutinin.
    • Anticancer drug-sensitive ovarian cancer cell lines exhibited minimal activity with specific lectins.

    Conclusions:

    • Lectin microarray analysis is effective in characterizing and distinguishing endometrial cancer from normal tissue.
    • This method can differentiate between endometrial cancer subtypes (G1 and G3) and cancer stages.
    • Glycan profiling using lectin microarrays holds promise for assessing tumor characteristics and predicting chemotherapy treatment success.