Literature DB >> 25292033

Germline variations of apurinic/apyrimidinic endonuclease 1 (APEX1) detected in female breast cancer patients.

Kashif Ali1, Ishrat Mahjabeen, Maimoona Sabir, Ruqia Mehmood Baig, Maryam Zafeer, Muhammad Faheem, Mahmood Akhtar Kayani.   

Abstract

Apurinic/apyrimidinic endonuclease 1 (APEX1) is a multifunctional protein which plays a central role in the BER pathway. APEX1 gene being highly polymorphic in cancer patients and has been indicated to have a contributive role in Apurinic/apyrimidinic (AP) site accumulation in DNA and consequently an increased risk of cancer development. In this case-control study, all exons of the APEX1 gene and its exon/intron boundaries were amplified in 530 breast cancer patients and 395 matched healthy controls and then analyzed by single-stranded conformational polymorphism followed by sequencing. Sequence analysis revealed fourteen heterozygous mutations, seven 5'UTR, one 3 'UTR, two intronic and four missense. Among identified mutations one 5'UTR (rs41561214), one 3'UTR (rs17112002) and one missense mutation (Ser129Arg, Mahjabeen et al., 2013) had already been reported while the remaining eleven mutations. Six novel mutations (g.20923366T>G, g.20923435G>A, g.20923462G>A, g.20923516G>A, 20923539G>A, g.20923529C>T) were observed in 5'UTR region, two (g.20923585T>G, g.20923589T>G) in intron1 and three missense (Glu101Lys, Ala121Pro, Ser123Trp) in exon 4. Frequencues of 5'UTR mutations; g.20923366T>G, g.20923435G>A and 3'UTR (rs17112002) werecalculated as 0.13, 0.1 and 0.1 respectively. Whereas, the frequency of missense mutations Glu101Lys, Ser123Trp and Ser129Arg was calculated as 0.05. A significant association was observed between APEX1 mutations and increased breast cancer by ~9 fold (OR=8.68, 95%CI=2.64 to 28.5) with g.20923435G>A (5'UTR) , ~13 fold (OR= 12.6, 95%CI=3.01 to 53.0) with g.20923539G>A (5'UTR) and~5 fold increase with three missense mutations [Glu101Lys (OR=4.82, 95%CI=1.97 to 11.80), Ser123Trp (OR=4.62, 95%CI=1.7 to 12.19), Ser129Arg (OR=4.86, 95%CI=1.43 to 16.53)]. The incidence of observed mutations was found higher in patients with family history and with early menopause. In conclusion, our study demonstrates a significant association between germ line APEX1 mutations and breast cancer patients in the Pakistani population.

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Year:  2014        PMID: 25292033     DOI: 10.7314/apjcp.2014.15.18.7589

Source DB:  PubMed          Journal:  Asian Pac J Cancer Prev        ISSN: 1513-7368


  3 in total

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Authors:  Ara Cho; Jung Eun Shim; Eiru Kim; Fran Supek; Ben Lehner; Insuk Lee
Journal:  Genome Biol       Date:  2016-06-23       Impact factor: 13.583

2.  DNA Repair Molecular Beacon assay: a platform for real-time functional analysis of cellular DNA repair capacity.

Authors:  Jianfeng Li; David Svilar; Steven McClellan; Jung-Hyun Kim; Eun-Young Erin Ahn; Conchita Vens; David M Wilson; Robert W Sobol
Journal:  Oncotarget       Date:  2018-08-03

3.  Identification of Breast Cancer Subtype-Specific Biomarkers by Integrating Copy Number Alterations and Gene Expression Profiles.

Authors:  Claudia Cava; Mirko Pisati; Marco Frasca; Isabella Castiglioni
Journal:  Medicina (Kaunas)       Date:  2021-03-12       Impact factor: 2.430

  3 in total

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