Przybylowska Karolina, Kluczna Anita, Zadrozny Marek, Krawczyk Tadeusz, Kulig Andrzej, Rykala Jan, Kolacinska Agnieszka, Morawiec Zbigniew, Drzewoski Jozef, Blasiak Janusz
Department of Molecular Genetics, University of Lodz, Lodz, Poland.
Breast Cancer Res Treat. 2006 Jan;95(1):65-72. doi: 10.1007/s10549-005-9042-6. Epub 2005 Nov 3.
Matrix metalloproteinases play a crucial role in the cancer invasion and metastasis, angiogenesis and tumorigenicity. A single guanine insertion--the 1G/2G polymorphism in the promoter of the matrix metalloproteinase 1 (MMP-1) gene creates a binding site for the transcription factor AP-1 and thus may affect the transcription level of MMP-1. The C-->T substitution at the polymorphic site of the MMP-9 gene promoter results in a higher transcription activity of the T-allelic promoter trough the loss of binding site for a repressor protein. The aim of this work was to investigate the influence of 1G/2G and C-->T polymorphisms on the MMP-1 and MMP-9 level and therefore on the occurrence and progression of breast cancer.
We investigated the distribution of genotypes and frequency of alleles of the 1G/2G and C-->T polymorphisms for 270 patients with breast cancer and 300 healthy women served as control. The genotypes were determined by RFLP-PCR. Additionally, we estimated the level of MMP-1 and MMP-9 antigens in tumor samples and normal breast tissue using ELISA.
The levels of MMP-1 in tumor samples of node positive patients ware significantly higher than in samples of node negative patients (p<0.05). Increased level of MMP-9 correlates with Bloom-Richardson grading III (p<0.05), increased tumor size (p<0.05) and absence of estrogen and progesterone receptors (p<0.01). Additionally, both MMP-1 and MMP-9 levels were higher in tumor than in the normal breast tissue. We showed the higher risk of metastasis development in lymph node for the 2G/2G genotype (OR=2.14; CI 95% 1.24;3.69) and the 2G allele carriers (OR=1.68; CI 95% 1.19;2.39). We found correlation between the T allele (OR=2.61; CI 95% 1.33;4.87), 2G (OR=2.58; CI 95% 1.35;4.91) and malignance.
The results suggest that MMP-1 is responsible for the local invasion and MMP-9 is associated with the malignance and the growth of the tumor. We suggest that the 2G allele of the 1G/2G MMP-1 gene polymorphism may be associated with the lymph node metastasis in patients with breast cancer and therefore it can be considered as a progression marker in this disease.
基质金属蛋白酶在癌症侵袭、转移、血管生成和肿瘤发生中起关键作用。单个鸟嘌呤插入——基质金属蛋白酶1(MMP-1)基因启动子中的1G/2G多态性产生了转录因子AP-1的结合位点,因此可能影响MMP-1的转录水平。MMP-9基因启动子多态性位点的C→T替换导致T等位基因启动子因阻遏蛋白结合位点的缺失而具有更高的转录活性。本研究旨在探讨1G/2G和C→T多态性对MMP-1和MMP-9水平的影响,进而对乳腺癌发生和进展的影响。
我们调查了270例乳腺癌患者和300名健康女性作为对照的1G/2G和C→T多态性的基因型分布和等位基因频率。通过限制性片段长度多态性聚合酶链反应(RFLP-PCR)确定基因型。此外,我们使用酶联免疫吸附测定(ELISA)估计肿瘤样本和正常乳腺组织中MMP-1和MMP-9抗原的水平。
淋巴结阳性患者肿瘤样本中MMP-1水平显著高于淋巴结阴性患者样本(p<0.05)。MMP-9水平升高与布卢姆-理查森分级III级(p<0.05)、肿瘤大小增加(p<0.05)以及雌激素和孕激素受体缺失(p<0.01)相关。此外,肿瘤中MMP-1和MMP-9水平均高于正常乳腺组织。我们发现2G/2G基因型(比值比[OR]=2.14;95%置信区间[CI]1.24;3.69)和2G等位基因携带者(OR=1.68;CI 95% 1.19;2.39)发生淋巴结转移的风险更高。我们发现T等位基因(OR=2.61;CI 95% 1.33;4.87)、2G(OR=2.58;CI 95% 1.35;4.91)与恶性程度之间存在相关性。
结果表明MMP-1负责局部侵袭,MMP-9与肿瘤的恶性程度和生长相关。我们认为1G/2G MMP-1基因多态性的2G等位基因可能与乳腺癌患者的淋巴结转移相关,因此可被视为该疾病的进展标志物。