Howard J C, Li Q, Chu W, Zochodne B, Kapoor M, Ung Y, Rosen K, Ben-David Y
Department of Medical Biophysics, University of Toronto, Division of Cancer Biology, Sunnybrook and Women's College Health Sciences Centre & Toronto-Sunnybrook Regional Cancer Centre, Toronto, Ontario, Canada.
Oncogene. 2001 Apr 26;20(18):2291-300. doi: 10.1038/sj.onc.1204348.
Erythroleukemias induced by various strains of Friend virus are multistage malignancies that result from the accumulation of genetic mutations, including the activation of proto-oncogenes and the inactivation of tumor suppressor genes. In this study, we demonstrate that Bcl-2 expression is activated in the majority of F-MuLV-induced erythroleukemia cell lines. In contrast, Bcl-2 was not expressed in any of the FV-P-induced erythroleukemia cell lines and protein levels were low or negligible in FV-A-induced erythroleukemia cell lines examined. In vivo, Bcl-2 expression levels gradually increased in F-MuLV-induced erythroleukemic cells prior to adaptation to culture. High expression of Bcl-2 in F-MuLV-induced erythroleukemic cells was shown to proceed the emergence of p53 mutation suggesting that Bcl-2 expression may delay p53 mutation in the leukemic cells. This is further supported by the demonstration that the majority of F-MuLV-induced erythroleukemia cell lines established from primary tumors induced in p53 mutant mice express low to negligible levels of Bcl-2. We have shown that the high levels of Bcl-2 expression in FV-P-induced erythroleukemic cells inhibited apoptosis induced by etoposide, low serum and p53 expression. Similarly, ectopic Bcl-2 expression within these cells also provided protection from apoptosis induced by etoposide and growth in low serum. These results suggest that the anti-apoptotic action of Bcl-2 may confer a selective in vivo and in vitro growth advantage to F-MuLV-induced erythroleukemic cells, which is not shared by FV-P/FV-A-induced erythroleukemic cells. The observed induction of Bcl-2 expression in vivo constitutes a novel but late oncogenic event associated with the progression of F-MuLV-induced erythroleukemias.
由不同株系的弗氏病毒诱导产生的红白血病是多阶段恶性肿瘤,由基因突变的积累导致,包括原癌基因的激活和肿瘤抑制基因的失活。在本研究中,我们证明在大多数F-MuLV诱导的红白血病细胞系中Bcl-2表达被激活。相反,在任何FV-P诱导的红白血病细胞系中均未检测到Bcl-2表达,并且在所检测的FV-A诱导的红白血病细胞系中其蛋白水平很低或可忽略不计。在体内,F-MuLV诱导的红白血病细胞在适应培养之前,Bcl-2表达水平逐渐升高。F-MuLV诱导的红白血病细胞中Bcl-2的高表达先于p53突变的出现,这表明Bcl-2表达可能会延迟白血病细胞中p53突变的发生。从p53突变小鼠原发肿瘤建立的大多数F-MuLV诱导的红白血病细胞系中Bcl-2表达水平低至可忽略不计,这进一步支持了上述观点。我们已经表明,FV-P诱导的红白血病细胞中高水平的Bcl-2表达可抑制依托泊苷、低血清和p53表达诱导的细胞凋亡。同样,这些细胞中异位表达的Bcl-2也能保护细胞免受依托泊苷诱导的凋亡以及在低血清中生长的影响。这些结果表明,Bcl-2的抗凋亡作用可能赋予F-MuLV诱导的红白血病细胞在体内和体外的选择性生长优势,而FV-P/FV-A诱导的红白血病细胞则不具备这种优势。在体内观察到的Bcl-2表达的诱导是与F-MuLV诱导的红白血病进展相关的一个新的但较晚期的致癌事件。