scholarly journals Occupational exposure to solvents and acute myeloid leukemia: a population-based, case–control study in four Nordic countries

2014 ◽  
Vol 40 (5) ◽  
pp. 511-517 ◽  
Author(s):  
Madar Talibov ◽  
Susanna Lehtinen-Jacks ◽  
Jan Ivar Martinsen ◽  
Kristina Kjærheim ◽  
Elsebeth Lynge ◽  
...  
Keyword(s):  
Acute Myeloid Leukemia ◽  
Occupational Exposure ◽  
Myeloid Leukemia ◽  
Case Control Study ◽  
Population Based ◽  
Case Control ◽  
Nordic Countries ◽  
Control Study ◽  
Acute Myeloid

scholarly journals NSAID consumption and risk of acute myeloid leukemia: a national population-based case-control study

2018 ◽  
Vol Volume 10 ◽  
pp. 5043-5051 ◽  
Author(s):  
Lene Østgård ◽  
Mette Nørgaard ◽  
Lars Pedersen ◽  
René Østgård ◽  
Lone Friis ◽  
...  
Keyword(s):  
Acute Myeloid Leukemia ◽  
Myeloid Leukemia ◽  
Case Control Study ◽  
Population Based ◽  
Case Control ◽  
National Population ◽  
Nsaid Consumption ◽  
Control Study ◽  
Acute Myeloid

scholarly journals Genetic Variants of ATM & Non-Homologous End Joining Pathway Genes in Acute Myeloid Leukemia: A South India Case-Control Study

Blood ◽  
2019 ◽  
Vol 134 (Supplement_1) ◽  
pp. 5076-5076
Author(s):  
Sugunakar Vuree ◽  
Anuradha Cingeetham ◽  
Dunna Nageswara Rao ◽  
Manjula Gorre ◽  
Sudha Sinha ◽  
...  
Keyword(s):  
Dna Repair ◽  
Acute Myeloid Leukemia ◽  
Myeloid Leukemia ◽  
Case Control Study ◽  
Case Control ◽  
South Indian Population ◽  
End Joining ◽  
Non Homologous End Joining ◽  
Control Study ◽  
Acute Myeloid

Purpose of the study: Deregulated DNA repair is one of the hallmarks of cancers including Acute Myeloid Leukemia (AML), as it results in genomic instability. ATM gene functions as a sensor, activates cascade of events leading to stimulation of multiple DNA damage- responsive signaling pathways. Principal DNA repair mechanism activated in the hematopoietic stem cells is the Non Homologous End Joining (NHEJ) pathway. However, this pathway was shown to be error prone. Functional SNPs in the genes involved in DNA repair might influence the gene expression leading to altered DNA repair which might confer the risk to AML. Materials & Methods: This hospital-based case-control study included 225 AML patients and 326 cancer-free controls from South Indian population. Six polymorphisms of XRCC5, XRCC6, XRCC7 and ATM were genotyped using polymerase chain reaction (PCR)-Restriction Fragment Length Polymorphism (PCR- RFLP) method. Statistical analyses were performed by using SPSS (version20v) and SNPSTAT online tool. Protein-Protein Interaction (PPI) analysis was also done to see the relationship between these genes. Results: We found that there was an elevated risk of AML associated with the XRCC5 VNTR 0R repeat and A allele of 2408G>A polymorphism (p-0.04 and p<0.0001 respectively), the frequencies of G allele (p-<0.0001) of XRCC6 -1310C>G and T allele (p-0.003) of ATM -5144A>T polymorphisms were also significantly increased in AML cases. Further, analyses of the variant genotypes with epidemiological and clinical variables revealed a significant association of the risk genotypes with development and progression of AML. Conclusion: The XRCC5 0R repeat, 2408G>A, XRCC6 -1310 C>G and ATM- 5144A>T polymorphisms, but not XRCC6 -61C>G and XRCC7 6721G>T polymorphisms, play an important role in the pathogenesis of AML. Figure Disclosures No relevant conflicts of interest to declare.

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