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Overexpression of LC3A autophagy protein in follicular and diffuse large B-cell lymphomas.

Authors :
Giatromanolaki A
Koukourakis MI
Pouliliou S
Gatter KC
Pezzella F
Harris AL
Sivridis E
Source :
Hematology/oncology and stem cell therapy [Hematol Oncol Stem Cell Ther] 2013 Mar; Vol. 6 (1), pp. 20-5. Date of Electronic Publication: 2013 Feb 28.
Publication Year :
2013

Abstract

Background and Objectives: Autophagy is a self-degradation mechanism induced under stress conditions in all eukaryotic cells. Its activity in human lymphomas has not been studied as yet.<br />Methods: In this study, the autophagic activity of lymphoid cells was investigated in follicular lymphomas (FL; 48 cases), diffuse large B-cell lymphomas (DLBCL; 78 cases), and in reactive follicular hyperplasias (41 cases), using the light chain 3A (LC3A) antibody and a standard immunohistochemical technique.<br />Results: In all cases, the pattern of LC3A reactivity was uniformly diffuse cytoplasmic, but expressed more frequently in FLs (68.8%) than in DLBCLs (41%) (p=0.02), and much more commonly in DLBCLs than in reactive lymph nodes (24.3%) (p<0.006). Interestingly, FLs expressing LC3A in >10% of lymphoid cells (high reactivity) were associated with the hypoxia-related protein HIF1α and the enzyme of anaerobic metabolism lactate dehydrogenase LDH5 (p=0.004 and p=0.003, respectively). Such associations, however, were not a feature in DLBCLs of increased LC3A activity.<br />Conclusions: LC3A expression in FLs is hypoxia-induced, whereas its expression in DLBCLs may be regulated by other molecular mechanisms. The current study provides a tool for further assessment of autophagic activity in translational and autophagy targeting therapy studies.<br /> (Copyright © 2013 King Faisal Specialist Hospital & Research Centre. Published by Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
2589-0646
Volume :
6
Issue :
1
Database :
MEDLINE
Journal :
Hematology/oncology and stem cell therapy
Publication Type :
Academic Journal
Accession number :
23664601
Full Text :
https://doi.org/10.1016/j.hemonc.2013.02.001