Autophagy-active beclin-1 correlates with favourable clinical outcome in non-Hodgkin lymphomas

• DOI: 10.1038/modpathol.2010.80
• Publication Date: 2010-05-14T14:02:55Z
• Authors: Giuseppina Nicotra; Francesca Mercalli; Claudia Peracchio; Roberta Castino; Carlo Follo; Guido Valente; Ciro Isidoro
• Keywords: Adult; Aged, 80 and over; Male; 0303 health sciences; Lymphoma, Non-Hodgkin; Blotting, Western; Fluorescent Antibody Technique; Membrane Proteins; Kaplan-Meier Estimate; Middle Aged; Prognosis; 3. Good health; 03 medical and health sciences; Autophagy; Biomarkers, Tumor; Humans; Beclin-1; Female; Apoptosis Regulatory Proteins; Aged; Neoplasm Staging; Proportional Hazards Models

The expression of beclin-1, an oncosuppressor monoallelically deleted in >60% epithelial cancers, has been shown to be developmentally regulated in T and B lymphocytes. By interacting with either bcl-2 or class III phosphatidyl-inositol-3-phosphate kinase, beclin-1 regulates apoptosis and autophagy, two processes crucial for lymphatic tissue homeostasis. We analyzed the potential link between beclin-1-mediated autophagy and the malignant behaviour of lymphomas. The tissue expression of beclin-1 was analyzed in a large series of non-Hodgkin lymphomas and correlated with patient's clinical outcome. By immunofluorescence, beclin-1 staining showed faintly detectable and diffusely distributed in the cytoplasm (regarded as negative) or confined to the perinuclear region as large and brilliant puncta suggestive of macro-aggregate reactivity (regarded as positive). The positive expression of beclin-1 well correlated with the presence of LC3-positive autophagic vacuoles and was inversely correlated with the expression of bcl-2. Non-Hodgkin lymphomas in which > or =20% of tumour cells expressed high level of beclin-1 aggregates were associated with a complete (57%) or partial (35%) remission. The 5-year overall survival probability, calculated by the Kaplan-Meier method, was 92% and 42% in beclin-1-expressing non-Hodgkin lymphomas with > or =20% and <20% positive cells, respectively (log-rank test, P<0.000.1). In Cox multivariate analysis, the level of beclin-1 expression, adjusted for patient's age and pathologic stage, revealed to be significantly correlated with patient's survival (P<0.0001). This is the first demonstration of the involvement of beclin-1 and autophagy in the clinical behaviour of non-Hodgkin lymphomas. The present data are compatible with the hypothesis that non-Hodgkin lymphomas with upregulated autophagy are more responsive to chemotherapy and indicate that beclin-1 could be a valuable independent prognostic factor in this heterogeneous group of tumours.