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Updated: Jun 2, 2026

Isolation, Culture, and Characterization of Prostate Cancer-Associated Fibroblasts
Published on: August 1, 2025
Glycophenotype of prostatic carcinomas
M N Khabaz1, J McClure, S McClure
1Department of Pathology, Faculty of Medicine, Jordan University of Science and Technology, Irbid, Jordan. nkhabaz@yahoo.co.uk
Prostate cancer cells show altered glycosylation patterns, including changes in fucosylation and galactosylation, and express Lewis antigens not found in normal prostate tissue. These glycophenotypic changes are linked to cancer progression.
Area of Science:
- Biochemistry
- Oncology
- Glycobiology
Background:
- Carbohydrate antigens on tumor cell surfaces influence prostate cancer progression and metastasis.
- Understanding glycosylation changes is crucial for identifying potential biomarkers and therapeutic targets.
Purpose of the Study:
- To investigate alterations in glycosylation patterns in prostatic carcinoma compared to benign prostate tissue.
- To identify specific changes in oligosaccharide sequences and Lewis antigen expression.
Main Methods:
- Comparative lectin-histochemical analysis of 27 prostatic carcinoma and benign prostate samples.
- Utilized fifteen biotinylated lectins and monoclonal antibodies against Lewis antigens.
- Employed a semi-quantitative study to analyze staining intensity and binding patterns.
Main Results:
- Prostatic carcinoma exhibited distinct glycophenotypes with increased staining for several lectins (AAA, UEA-1, DBA, WFA, VVA, HPA, BSA-1B4, MPA, ECA, AHA, CTA).
- Lewis antigens (Lewisa, sialyl Lewisa, sialyl Lewisx) were expressed in carcinomas but absent in benign tissues.
- Observed increased fucosylation, galactosylation, branching, and sialylation on O-glycans in cancer cells.
Conclusions:
- Prostate cancer cells undergo significant glycophenotypic modifications.
- These changes involve altered fucosylation, galactosylation, and sialylation patterns, particularly on O-glycans.
- The expression of Lewis antigens in carcinoma suggests their potential role in cancer development or progression.
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