Peschos D, Damala C, Stefanou D, Tsanou E, Assimakopoulos D, Vougiouklakis T, Charalabopoulos K, Agnantis N J
Department of Forensic Medicine, Medical School, University of Ioannina, Ioannina, Greece.
Histol Histopathol. 2006 Jun;21(6):603-8. doi: 10.14670/HH-21.603.
The matrix metalloproteinases (MMPs) are a family of proteolytic zinc-containing enzymes, which are responsible for the breakdown of the extracellular matrix components in pathological and physiological conditions. They are involved in basement membrane disruption, stroma and blood vessel penetration, metastasis and more recently there is evidence that they participate in tumor growth and angiogenic events. Matrix metalloproteinase 2 and 9 (MMP 2 and 9) belong to the gelatinases, a subgroup of MMPs, and have the capacity to degrade the triple helix type IV collagen of basal lamina of the basement membrane. With the present study, we tried to demonstrate the expression of MMP-9 immunohistochemically, comparatively in benign, premalignant and malignant lesions of the larynx. We studied 154 laryngeal lesions including 55 squamous cell carcinomas, 8 in situ carcinomas, 54 cases of dysplasia (of low and intermediate grade), 13 papillomas and 24 cases of keratosis. Overexpression of MMP 9 was observed in 74.4% and 50% in invasive and in situ squamous cell carcinomas respectively. In dysplastic cases, in papillomas and in keratoses the percentage of overexpression was 62.9%, 61.53% and 54.16% respectively and the expression of MMP-9 was significantly higher in invasive squamous cell carcinomas compared to dysplasias (p=0.000004). Also significantly higher was the expression of MMP-9 in dysplastic cases compared to papillomas (p=0.023). The MMP-9 expression was related neither to survival nor to the other available clinicopathological parameters (tumor size, grade, clinical stage, lymph node status and patient age). In conclusion, our study indicates that the expression of MMP-9 is up-regulated in a stepwise fashion, with two main steps, the first one, when a dysplastic lesion evolves and the next one, when the dysplasia progresses to invasive carcinoma.
基质金属蛋白酶(MMPs)是一类含锌的蛋白水解酶家族,在病理和生理条件下负责细胞外基质成分的分解。它们参与基底膜破坏、基质和血管浸润、转移,最近有证据表明它们参与肿瘤生长和血管生成事件。基质金属蛋白酶2和9(MMP 2和9)属于明胶酶,是MMPs的一个亚组,具有降解基底膜基底层的三螺旋IV型胶原蛋白的能力。在本研究中,我们试图通过免疫组织化学方法比较喉良性、癌前和恶性病变中MMP - 9的表达。我们研究了154例喉部病变,包括55例鳞状细胞癌、8例原位癌、54例(低级别和中级别的)发育异常、13例乳头状瘤和24例角化病。侵袭性和原位鳞状细胞癌中MMP 9的过表达率分别为74.4%和50%。在发育异常病例、乳头状瘤和角化病中,过表达率分别为62.9%、61.53%和54.16%,与发育异常相比,侵袭性鳞状细胞癌中MMP - 9的表达显著更高(p = 0.000004)。与乳头状瘤相比,发育异常病例中MMP - 9的表达也显著更高(p = 0.023)。MMP - 9的表达与生存率以及其他可用的临床病理参数(肿瘤大小、分级、临床分期、淋巴结状态和患者年龄)均无关。总之,我们的研究表明,MMP - 9的表达呈逐步上调,主要有两个阶段,第一个阶段是发育异常病变的演变,第二个阶段是发育异常进展为侵袭性癌。