BAX/BCL-XL gene expression ratio inversely correlates with disease progression in chronic myeloid leukemia

Abstract

BCR-ABL fusion gene is implicated in the pathogenesis of chronic myeloid leukemia (CML), encoding the oncoprotein p210 BCR-ABL with an anti-apoptotic activity. The inability to undergo apoptosis is an important mechanism of drug resistance and neoplastic evolution in CML. The gene transcript expression of mitochondrial apoptotic related genes BAX and BCL-XL were evaluated by quantitative Real Time PCR (qPCR) in vitro in K562 cells and in vivo in peripheral blood of 66 CML patients in different stages of the disease: 13 cases at diagnosis, 34 in chronic phase (CP), 10 in accelerated phase (AP) and 9 in blast crisis (BC). Our results in K562 cells showed that all treatments with different tyrosine kinase inhibitors (TKIs) induced a decreased expression of the antiapoptotic oncogene BCL-XL, whereas the proapoptotic gene BAX remains constant with minor modifications. A significantly lower BAX/BCL-XL expression ratio (mean ± SEM) than a group of healthy individuals (4.8 ± 0.59) were observed in CML patients at diagnosis (1.28 ± 0.16), in AP (1.14 ± 0.20), in BC (1.16 ± 0.30) and in 18% of cases of patients in CP (2.71 ± 0.40). Most CP cases (82%) showed a significantly increased ratio (10.03 ± 1.30), indicating that the treatment with TKIs efficiently inhibited the expression of BCL-XL by blocking BCR-ABL oncoprotein. The BAX/BCL-XL ratio showed a significant inverse correlation (Spearman P< 0.0001) with BCR-ABL/ABL relative expression indicating that low BAX/BCL-XL associated with disease progression. Accordingly, the follow up of a cohort of eight cases during 6 months from diagnosis showed that while the BAX/BCL-XL ratio rapidly increased after treatment in seven cases with good evolution, it decreased in the only one case that showed bad evolution and short survival. Our data suggest that BAX/BCL-XL expression ratio may be a sensitive monitor of disease progression and an early predictor of TKI therapy responsiveness in CML patients.