The G(-248)A polymorphism in the promoter region of the Bax gene does not correlate with prognostic markers or overall survival in chronic lymphocytic leukemia

• Published in: Leukemia Vol. 20; no. 1; pp. 77 - 81
• Main Authors: Skogsberg, S, Tobin, G, Kröber, A, Kienle, D, Thunberg, U, Aleskog, A, Karlsson, K, Laurell, A, Merup, M, Vilpo, J, Sundström, C, Roos, G, Jernberg-Wiklund, H, Döhner, H, Nilsson, K, Stilgenbauer, S, Rosenquist, R
• Format: Journal Article
• Language: English
• Published: England Nature Publishing Group 01-01-2006
• Subjects: Adult; Aged; Aged, 80 and over; Bax promoter polymorphism; bcl-2-Associated X Protein - biosynthesis; bcl-2-Associated X Protein - genetics; bcl-2-Associated X Protein/biosynthesis/genetics; Binet stage; Biomarkers, Tumor - biosynthesis; Biomarkers, Tumor - genetics; Chronic lymphocytic leukemia; Cohort Studies; Cytogenetic Analysis; Female; Genomic aberrations; Humans; Immunoglobulin VH gene mutation status; Leukemia, Lymphocytic, Chronic, B-Cell - diagnosis; Leukemia, Lymphocytic, Chronic, B-Cell - genetics; Male; Medicin och hälsovetenskap; Middle Aged; NATURAL SCIENCES; NATURVETENSKAP; Polymorphism, Genetic - genetics; Prognosis; Promoter Regions (Genetics); Promoter Regions, Genetic; Retrospective Studies; Survival Rate; 80 and over; Genetic/genetics; Lymphocytic; Leukemia; Chronic/diagnosis/genetics; Biological/biosynthesis/genetics; Aged; Tumor Markers; Polymorphism
• ISSN: 0887-6924; 1476-5551; 1476-5551
• DOI: 10.1038/sj.leu.2404030

The G(-248)A polymorphism in the promoter region of the Bax gene was recently associated with low Bax expression, more advanced stage, treatment resistance and short overall survival in B-cell chronic lymphocytic leukemia (CLL), the latter particularly in treated patients. To investigate this further, we analyzed 463 CLL patients regarding the presence or absence of the G(-248)A polymorphism and correlated with overall survival, treatment status and known prognostic factors, for example, Binet stage, VH mutation status and genomic aberrations. In this material, similar allele and genotype frequencies of the Bax polymorphism were demonstrated in CLL patients and controls (n=207), where 19 and 21% carried this polymorphism, respectively, and no skewed distribution of the polymorphism was evident between different Binet stages and VH mutated and unmutated CLLs. Furthermore, no difference in overall survival was shown between patients displaying the G(-248)A polymorphism or not (median survival 85 and 102 months, respectively, P=0.21), and the polymorphism did not influence outcome specifically in treated CLL. Neither did the polymorphism affect outcome in prognostic subsets defined by VH mutation status or genomic aberrations. In conclusion, the pathogenic role and clinical impact of the Bax polymorphism is limited in CLL.