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http://dx.doi.org/10.7314/APJCP.2016.17.2.815

Significance of ATM Gene Polymorphisms in Chronic Myeloid Leukemia - a Case Control Study from India  

Gorre, Manjula (Department of Genetics, Osmania University)
Mohandas, Prajitha Edathara (Department of Genetics, Osmania University)
Kagita, Sailaja (Homibhabha Cancer Hospital and Research Centre)
Cingeetham, Anuradha (Jawaharlal Nehru Technological University)
Vuree, Sugunakar (Department of Genetics, Osmania University)
Jarjapu, Sarika (Department of Genetics, Osmania University)
Nanchari, Santhoshirani (Department of Genetics, Osmania University)
Meka, Phanni Bhushann (Department of Genetics, Osmania University)
Annamaneni, Sandhya (Department of Genetics, Osmania University)
Dunna, Nageswara Rao (Shastra University)
Digumarti, Raghunadharao (Homibhabha Cancer Hospital and Research Centre)
Satti, Vishnupriya (Department of Genetics, Osmania University)
Publication Information
Asian Pacific Journal of Cancer Prevention / v.17, no.2, 2016 , pp. 815-821 More about this Journal
Abstract
Background: Development of chronic myeloid leukemia (CML) involves formation of double strand breaks (DSBs) which are initially sensed by the ataxia telangiectasia mutated (ATM) signal kinase to induce a DNA damage response (DDR). Mutations or single nucleotide polymorphisms in ATM gene are known to influence the signaling capacity resulting in susceptibility to certain genetic diseases such as cancers. Materials and Methods: In the present study, we have analyzed -5144A>T (rs228589) and C4138T (rs3092856) polymorphisms of theATM gene through polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) in 925 subjects (476 CML cases and 449 controls). Results: The A allele of -5144A>T polymorphism and T allele of C4138T polymorphism which were known to be influencing ATM signaling capacity are significantly associated with enhanced risk for CML independently and also in combination (evident from the haplotype and diplotype analyses). Significant elevation in the frequencies of both the risk alleles among high risk groups under European Treatment and Outcome Study (EUTOS) score suggests the possible role of these polymorphisms in predicting the prognosis of CML patients. Conclusions: This study provides the first evidence of association of functional ATM gene polymorphisms with the increased risk of CML development as well as progression.
Keywords
Chronic myeloid leukemia; ATM-5144A>T; C4138T; EUTOS score; progression;
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