Gelatinase B (-1562C/T) polymorphism in tumor progression and invasion of breast cancer

被引:35
作者
Chiranjeevi, P. [1 ]
Spurthi, K. Mrudula [1 ]
Rani, N. Santhoshi [1 ]
Kumar, G. Rajesh [1 ]
Aiyengar, T. Mohini [1 ]
Saraswati, M. [1 ]
Srilatha, G. [1 ]
Kumar, G. Kishore [1 ]
Sinha, Sudha [2 ,3 ]
Kumari, C. Sanjeeva [2 ,3 ]
Reddy, B. Nagarjuna [2 ,3 ]
Vishnupriya, S. [1 ]
Rani, H. Surekha [1 ]
机构
[1] Osmania Univ, Dept Genet, Hyderabad 500007, Andhra Pradesh, India
[2] MNJ Inst Oncol, Hyderabad, Andhra Pradesh, India
[3] Reg Canc Ctr, Hyderabad, Andhra Pradesh, India
关键词
Breast cancer; Tumor invasion; Allele specific; Genotyping; Matrix metalloproteinases; MMP-9; gene; MATRIX METALLOPROTEINASES; INCREASED EXPRESSION; MATRIX-METALLOPROTEINASE-9; MMP-9; RISK; PROGNOSIS; PROMOTER; SUSCEPTIBILITY; METASTASIS; INHIBITORS;
D O I
10.1007/s13277-013-1181-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Matrix metalloproteinases (MMPs) play an important role in breast cancer tumor invasion and progression. MMP-9 is a member of the MMP family and is also known as Gelatinase B or type IV collagenases (92 kDa) and possesses proteolytic activity against type IV collagen, a major component of the basement membrane. Our study aims to examine the association of Gelatinase B (-1562C > T) promoter polymorphism with breast cancer invasion and progression. The study involves 200 breast cancer patients and age-matched 191 healthy controls. The SNP-1562C > T (rs3918242) in MMP-9 promoter region was examined by allele-specific polymerase chain reaction and gel electrophoresis. The genotypes were determined and compared between patients and controls, and the influence of the polymorphism on clinicopathological data was analyzed. The T allele of the -1562C > T MMP-9 polymorphism was detected more frequently in breast cancer patients than controls (p < 0.001). Our results suggest the clinical importance of MMP-9 gene polymorphism (-1562C > T) in breast cancer patients. The study may also help in identifying individuals at risk of developing breast cancer.
引用
收藏
页码:1351 / 1356
页数:6
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