Dysregulation of autophagy in human follicular lymphoma is independent of overexpression of BCL-2

• Published in: Oncotarget 2014-11, Vol.5 (22), p.11653-11668
• Main Authors: McCarthy, Aine, Marzec, Jacek, Clear, Andrew, Petty, Robert D, Coutinho, Rita, Matthews, Janet, Wilson, Andrew, Iqbal, Sameena, Calaminici, Maria, Gribben, John G, Jia, Li
• Format: Article
• Language: English
• Subjects: Antigens, CD - metabolism; Antigens, Differentiation, Myelomonocytic - metabolism; Apoptosis Regulatory Proteins - metabolism; Autophagy; B-Lymphocytes - metabolism; Beclin-1; Biopsy; Cathepsin D - metabolism; Cell Line, Tumor; DNA, Complementary - metabolism; Flow Cytometry; Gene Expression Profiling; Gene Expression Regulation; Gene Expression Regulation, Neoplastic; GTP-Binding Proteins - metabolism; Humans; Lymph Nodes - pathology; Lymphoma, Follicular - metabolism; Lymphoma, Follicular - pathology; Macrophages - metabolism; Membrane Proteins - metabolism; Microtubule-Associated Proteins - metabolism; Proto-Oncogene Proteins c-bcl-2 - metabolism; Research Paper; RNA-Binding Proteins - metabolism; Tissue Array Analysis; Transglutaminases - metabolism
• ISSN: 1949-2553; 1949-2553
• DOI: 10.18632/oncotarget.2605

Overexpression of the anti-apoptotic protein BCL-2 is characteristic of human follicular lymphoma (FL) and some cases of diffuse large B cell lymphoma (DLBCL). We aimed to determine autophagy status in primary FL and DLBCL samples and the BCL-2+/BCL-2- lymphoma cell lines using both autophagy PCR array and tissue microarray (TMA). A greater number of autophagy machinery genes were up-regulated in the BCL-2+ Su-DHL4 cell line compared with BCL-2- Su-DHL8 cells, at both the basal level and in response to autophagic stress. The autophagy-related gene expression profiles were determined in purified and unpurified malignant human lymph node biopsies. Seven autophagy machinery genes were up-regulated in purified FL B-cells compared with reactive B-cells. Only 2 autophagy machinery genes were up-regulated in DLBCL B-cells. In unpurified tissue biopsies, 20 of 46 genes in FL and 2 of 5 genes in DLBCL with increased expression were autophagy machinery genes. Expression of autophagy substrates p62 and LC3 were determined by TMAs. FL samples showed significantly decreased levels of both p62 and LC3 compared with reactive and DLBCL, indicative of an increased autophagy activity in FL. In summary, these results demonstrate that FL showed increased basal autophagy activity, regardless of overexpression of BCL-2 in this disease.