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Immunoglobulin Gene Sequence Analysis In Chronic Lymphocytic Leukemia: From Patient Material To Sequence Interpretation
Published on: November 26, 2018
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LGALS3 as a prognostic factor for classical Hodgkin's lymphoma
Young Wha Koh1, Se Jin Jung2, Chan-Sik Park3
1Department of Pathology, Ajou University School of Medicine, Suwon, Korea.
Summary
Galectin-3 (LGALS3) protein expression in tumor cells predicts poor survival in classical Hodgkin
Area of Science:
- Oncology
- Molecular Biology
- Immunology
Background:
- Galectin-3 (LGALS3) is a lectin involved in tumor progression by inhibiting apoptosis.
- LGALS3 shares structural similarities with BCL2, another protein implicated in cell survival.
- The prognostic value of LGALS3 and BCL2 in classical Hodgkin's lymphoma (cHL) requires further investigation.
Purpose of the Study:
- To evaluate the prognostic significance of LGALS3 and BCL2 expression in patients with classical Hodgkin's lymphoma.
- To determine if LGALS3 or BCL2 expression can predict survival outcomes in cHL.
- To identify potential therapeutic targets or patient subgroups requiring intensified treatment.
Main Methods:
- Retrospective analysis of diagnostic tissues from 110 uniformly treated cHL patients.
- Immunohistochemical assessment of LGALS3 and BCL2 protein expression in Hodgkin/Reed-Sternberg cells.
- Statistical analysis including survival analysis and multivariate analysis.
Main Results:
- LGALS3 protein expression was observed in 25% of patients and was significantly associated with poor overall survival (P=0.007) and event-free survival (P<0.001).
- BCL2 protein expression was found in 14% of patients but showed no association with survival outcomes (P=0.928 and P=0.900).
- LGALS3 was identified as an independent prognostic factor for event-free survival (P=0.007) and showed prognostic value in limited-stage cHL.
Conclusions:
- LGALS3 protein expression is an independent prognostic factor in classical Hodgkin's lymphoma.
- LGALS3 may help identify limited-stage cHL patients who could benefit from more intensive therapy.
- BCL2 expression did not demonstrate prognostic significance in this cohort.
