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Association Between Polymorphisms in Segregation Genes BUB1B and TTK and Gastric Cancer Risk

Overview
Journal Radiol Oncol
Publisher Sciendo
Specialties Oncology
Radiology
Date 2016 Sep 29
PMID 27679546
Citations 20
Authors
Affiliations
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Abstract

Background: Malignant transformation of normal gastric cells is a complex and multistep process, resulting in development of heterogeneous tumours. Susceptible genetic background, accumulation of genetic changes, and environmental factors play an important role in gastric carcinogenesis. Single nucleotide polymorphisms (SNPs) in mitotic segregation genes could be responsible for inducing the slow process of accumulation of genetic changes, leading to genome instability.

Patients And Methods: We performed a case-control study of polymorphisms in mitotic kinases TTK rs151658 and BUB1B rs1031963 and rs1801376 to assess their effects on gastric cancer risk. We examined the TTK abundance in gastric cancer tissues using immunoblot analysis.

Results: C/G genotype of rs151658 was more frequent in patients with diffuse type of gastric cancer and G/G genotype was more common in intestinal types of gastric cancers (p = 0.049). Polymorphic genotype A/A of rs1801376 was associated with higher risk for developing diffuse type of gastric cancer in female population (p = 0.007), whereas A/A frequencies were increased in male patients with subserosa tumour cell infiltration (p = 0.009). T/T genotype of rs1031963 was associated with well differentiated tumours (p = 0.035). TT+CT genotypes of rs1031963 and GG+AG genotypes of rs1801376 were significantly associated with gastric cancer risk (dominant model; OR = 2,929, 95% CI: 1.281-6.700; p = 0.017 and dominant model; OR = 0,364, 95% CI: 0.192-0.691; p = 0.003 respectively).

Conclusions: Our results suggest that polymorphisms in mitotic kinases TTK and BUB1B may contribute to gastric tumorigenesis and risk of tumour development. Further investigations on large populations and populations of different ethnicity are needed to determine their clinical utility.

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References
1.
Gonzalez C, Agudo A . Carcinogenesis, prevention and early detection of gastric cancer: where we are and where we should go. Int J Cancer. 2011; 130(4):745-53. DOI: 10.1002/ijc.26430. View

2.
Ling Y, Zhang X, Bai Y, Li P, Wei C, Song T . Overexpression of Mps1 in colon cancer cells attenuates the spindle assembly checkpoint and increases aneuploidy. Biochem Biophys Res Commun. 2014; 450(4):1690-5. DOI: 10.1016/j.bbrc.2014.07.071. View

3.
Grabsch H, Askham J, Morrison E, Pomjanski N, Lickvers K, Parsons W . Expression of BUB1 protein in gastric cancer correlates with the histological subtype, but not with DNA ploidy or microsatellite instability. J Pathol. 2004; 202(2):208-14. DOI: 10.1002/path.1499. View

4.
Tian W, Li B, Warrington R, Tomchick D, Yu H, Luo X . Structural analysis of human Cdc20 supports multisite degron recognition by APC/C. Proc Natl Acad Sci U S A. 2012; 109(45):18419-24. PMC: 3494910. DOI: 10.1073/pnas.1213438109. View

5.
Hewitt L, Tighe A, Santaguida S, White A, Jones C, Musacchio A . Sustained Mps1 activity is required in mitosis to recruit O-Mad2 to the Mad1-C-Mad2 core complex. J Cell Biol. 2010; 190(1):25-34. PMC: 2911659. DOI: 10.1083/jcb.201002133. View