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Thornborrow, E.C., Patel, S., Mastropietro, A.E., Schwartzfarb, E.M. and Manfredi, J.J. (2002) A Conserved Intronic Response Element Mediates Direct p53-Dependent Transcriptional Activation of Both the Human and Murine Bax Genes. Oncogene, 21, 990-999. http://dx.doi.org/10.1038/sj.onc.1205069

has been cited by the following article:

  • TITLE: BAX G(-248)A Gene Polymorphism and Its Association with Risk of Non-Small Cell Lung Cancer—A Case Control Study

    AUTHORS: Jamsheed Javid, Rashid Mir, Pramod Kumar Julka, Prakash Chandra Ray, Alpana Saxena

    KEYWORDS: BAX G(-248)A Polymorphism, PIRA-PCR, NSCLC Risk

    JOURNAL NAME: Open Journal of Apoptosis, Vol.4 No.2, April 29, 2015

    ABSTRACT: Pro-apoptotic Bcl-2 protein BAX is an important member of mitochondrial dependent apoptosis regulation and ultimately plays a pivotal role in malignancies. A promoter G(-248)A polymorphism in the TP53 binding region of BAX results in differential binding capacity of TP53 protein there by regulating its expression, which has been found to be associated with different clinical outcomes in various malignancies. Presently we aimed to analyze the possible impact of the BAX G(-248)A polymorphism on the risk and other clinical features of non-small cell lung cancer in Indian population. The BAX promoter polymorphism was analyzed in blood samples of 320 subjects with 1:1 case/control ratio by primer-introduced restriction analysis PCR and survival curves were plotted using Kaplan-Meier analysis. It was observed that more than 3-fold increased risk of developing non-small cell lung cancer was associated with homozygous AA genotype of BAX G(-248)A promoter polymorphism in Indian population, with more predominant in smokers with pack-year > 45 (heavy) and using cigarette or huka as their smoking source than homozygous GG genotype. Significant associations was observed between TNM stage (p = 0.037) and histological type (0.02), of non-small cell lung cancer patients with the polymorphism. Patients homozygous for A allele exhibited a significant poor overall survival compared with patients displaying GA + AA or GA or GG genotype [median survival 6.0 vs 9.0, 11.0, and 30.0 months, respectively (p