This case control study aims to investigate the role of MMP-2 -1306C>T polymorphism as a potential risk factor and possible prognostic marker for breast cancer in a South European population. 113 consecutive incident cases of histologically confirmed ductal breast cancer and 124 healthy controls were recruited. MMP-2 -1306C>T polymorphism was genotyped; multivariate logistic regression as well as Cox regression analysis were performed. MMP-2 -1306C>T status was not associated with breast cancer risk either at the total sample or at the subanalyses on premenopausal and postmenopausal women. At the survival analysis, a trend towards a favorable association between MMP-2 -1306C>T allele and disease-free survival as well as overall survival was observed. Regarding subanalyses on ER-negative and ER-positive cases, the favorable association implicating MMP-2 -1306C>T allele was particularly evident among ER-positive cases; no significant associations emerged among ER-negative cases. MMP-2 -1306C>T polymorphism does not seem to be a risk factor for breast cancer in South European population; however, a trend towards a favorable association with survival has been observed.

Download full-text PDF

Source
http://dx.doi.org/10.1007/s11033-013-2604-5DOI Listing

Publication Analysis

Top Keywords

mmp-2 -1306c>t
28
breast cancer
20
-1306c>t polymorphism
16
south european
12
european population
12
favorable association
12
risk factor
8
cancer south
8
trend favorable
8
-1306c>t allele
8

Similar Publications

Article Synopsis
  • - The study investigated the roles of genetic variations in the MTHFR and MMP-2 genes in individuals' susceptibility to bladder cancer in Turkey's Thrace region, using blood samples from 179 participants (98 patients and 81 healthy controls).
  • - Key findings indicated that the MTHFR A1298C CC genotype and the MMP-2 TT genotype were associated with increased risk of developing bladder cancer, while certain genotypes (AC for MTHFR and AC for MMP-2) acted as protective factors.
  • - The research concluded that specific gene combinations, particularly the CC-CC combined genotype of C677T/A1298C, were identified as significant genetic risk factors for bladder cancer development, highlighting the complexity
View Article and Find Full Text PDF

Association of matrix metalloproteinase-2 gene variants with diabetic nephropathy risk.

J Gene Med

November 2023

Laboratory of Human Genome and Multifactorial Diseases (LR12ES07), Faculty of Pharmacy of Monastir, University of Monastir, Monastir, Tunisia.

Background: Diabetic nephropathy is a highly destructive microvascular complication of diabetes. Genetic predisposition is involved in the pathogenesis of diabetic nephropathy, with multiple allelic polymorphisms associated with the development and progression of the disease, thereby increasing the overall risk. To date, no study is available that shows the association of matrix metalloproteinase-2 (MMP-2) gene polymorphisms with diabetic nephropathy risk.

View Article and Find Full Text PDF

Matrix Metalloproteinase-2 () and-9 () Gene Variants and Microvascular Complications in Type 2 Diabetes Patients.

Balkan J Med Genet

June 2022

Clinic for Endocrinology, Diabetes and Metabolic Diseases, Clinical Centre of Serbia, Faculty of Medicine, University of Belgrade, Belgrade, Serbia.

Vascular complications are the leading cause of increased morbidity and mortality of diabetic patients. It has been postulated that matrix metalloproteinases and , zinc-dependent endopeptidases through remodeling of the extracellular matrix, can contribute to the onset and progression of diabetic vascular complications. The aim of our study was to assess whether there is a major difference in single nucleotide polymorphisms in the (at position -1306C˃T) and (at position -1562C˃T) gene in type 2 diabetic patients and healthy controls and to determine whether there is an association of these gene variants with the presence of microvascular complications in diabetic patients.

View Article and Find Full Text PDF

Objective: To determine the associations between matrix metalloproteinase-2 (MMP-2, encoded by the gene) 1306C/T and 735C/T polymorphisms and first and recurrent ischemic stroke in a Chinese population.

Methods: Patients with first and recurrent ischemic stroke were included. Serum MMP-2 was measured, and 1306C/T and 735C/T polymorphisms were detected.

View Article and Find Full Text PDF

Objectives: Acute and chronic allograft rejection have been continuously an important obstacle in the follow-up of renal transplant recipients. During clinical management, several factors acting simultaneously result in acute rejection and chronic allograft nephropathy. Matrix metalloproteinases and tissue inhibitors of metalloproteinases are responsible for the organization of the extracellular matrix and play roles in cell proliferation and cellular invasion.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!