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基质金属蛋白酶(MMP - 2和 - 9)及其抑制剂(TIMP - 1和 - 2)在前列腺癌组织中的表达

Expression of matrix metalloproteinases (MMP-2 and -9) and their inhibitors (TIMP-1 and -2) in prostate cancer tissue.

作者信息

Brehmer B, Biesterfeld S, Jakse G

机构信息

Clinic of Urology, University Clinic Aachen, Germany.

出版信息

Prostate Cancer Prostatic Dis. 2003;6(3):217-22. doi: 10.1038/sj.pcan.4500657.

Abstract

Matrix metalloproteinases (MMPs) have been implicated in progression and metastases of different tumours. The balance between the MMPs and their natural inhibitors (tissue inhibitors of matrix metalloproteinases; TIMP) seems to be an important factor related to this role. Here, the expression of MMP-2 and -9 along with TIMP-1 and -2 was examined in prostate cancer tissue. A total of 40 radical prostatectomy specimens were embedded in paraffin and immunohistochemical staining was performed to detect MMP-2 and -9, and TIMP-1 and -2. The immunoreactivity was assessed semiquantitively using routine light microscopy. The intensity of staining was correlated to preoperative PSA, T category, Gleason score and clinical parameters of the specimens. The imbalance of MMPs and TIMPs was recognised as a significant loss of TIMP-1 in malignant epithelium and an upregulation of MMPs. Palpable tumours (T2, T3) expressed significantly more MMP-2 and significantly less MMP-9 than T1c tumours. Our data are in accordance with other literature reports in that an imbalance of MMPs and TIMPs is found in malignant tumours. The observed imbalance of MMP and TIMP is mainly caused by a loss of TIMP-1. Furthermore, palpable tumours demonstrated significantly more MMP-2 and significantly less MMP-9 expression than nonpalpable tumours.

摘要

基质金属蛋白酶(MMPs)与不同肿瘤的进展和转移有关。MMPs与其天然抑制剂(基质金属蛋白酶组织抑制剂;TIMP)之间的平衡似乎是与该作用相关的一个重要因素。在此,检测了前列腺癌组织中MMP-2和-9以及TIMP-1和-2的表达。总共40个前列腺癌根治术标本被石蜡包埋,并进行免疫组织化学染色以检测MMP-2和-9以及TIMP-1和-2。使用常规光学显微镜对免疫反应性进行半定量评估。染色强度与术前前列腺特异性抗原(PSA)、T分期、 Gleason评分以及标本的临床参数相关。MMPs和TIMPs的失衡表现为恶性上皮中TIMP-1的显著缺失以及MMPs的上调。可触及肿瘤(T2、T3)比T1c肿瘤表达显著更多的MMP-2和显著更少的MMP-9。我们的数据与其他文献报道一致,即在恶性肿瘤中发现了MMPs和TIMPs的失衡。观察到的MMP和TIMP失衡主要是由TIMP-1的缺失引起的。此外,可触及肿瘤比不可触及肿瘤表现出显著更多的MMP-2表达和显著更少的MMP-9表达。

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