Corte M D, Gonzalez L O, Corte M G, Quintela I, Pidal I, Bongera M, Vizoso F
Instituto Universitario de Oncología del Principado de Asturias, Oviedo, Spain.
Int J Biol Markers. 2005 Oct-Dec;20(4):242-8. doi: 10.1177/172460080502000407.
Matrix metalloproteases (MMPs), enzymes with the ability to degrade the extracellular matrix, play an important role in tissue invasion by cutaneous malignant melanoma (CMM). One specific MMP, collagenase-3 (MMP-13), is thought to have a key function in the activation of MMP.
To evaluate the expression of MMP-13 in CMM and assess its possible relationship to clinical and pathological parameters.
MMP-13 expression was analyzed in 51 paraffin-embedded tumor samples from patients with invasive CMM, ten samples from in situ melanomas, and in eight samples from benign lesions (three dermal melanocytic nevi, three compound melanocytic nevi and two atypical melanocytic nevi) using immunohistochemical techniques. The median follow-up period in patients with invasive CMM was 50 months.
Benign lesions were consistently negative for MMP-13, whereas three of the ten in situ melanomas (30%) and 23 of the 51 invasive CMMs (45%) showed positive immunostaining for MMP-13. The percentage of MMP-13-positive tumors correlated significantly and positively with the mitotic index (p=0.002) in invasive CMM. However, our results did not show any significant association between tumoral MMP-13 expression and relapse-free survival in patients with invasive CMM.
MMP-13 appears to be a factor associated with tumor aggressiveness in CMM. It seems to eliminate an important barrier not only against tumoral invasion but also against proliferation.
基质金属蛋白酶(MMPs)是一类具有降解细胞外基质能力的酶,在皮肤恶性黑色素瘤(CMM)的组织侵袭过程中发挥重要作用。一种特定的MMP,即胶原酶-3(MMP-13),被认为在MMP的激活中起关键作用。
评估MMP-13在CMM中的表达,并评估其与临床和病理参数的可能关系。
采用免疫组织化学技术,对51例浸润性CMM患者的石蜡包埋肿瘤样本、10例原位黑色素瘤样本以及8例良性病变样本(3例真皮黑素细胞痣、3例复合性黑素细胞痣和2例非典型黑素细胞痣)进行MMP-13表达分析。浸润性CMM患者的中位随访期为50个月。
良性病变的MMP-13始终呈阴性,而10例原位黑色素瘤中有3例(30%)和51例浸润性CMM中有23例(45%)的MMP-13免疫染色呈阳性。在浸润性CMM中,MMP-13阳性肿瘤的百分比与有丝分裂指数显著正相关(p=0.002)。然而,我们的结果并未显示肿瘤MMP-13表达与浸润性CMM患者无复发生存之间存在任何显著关联。
MMP-13似乎是与CMM肿瘤侵袭性相关的一个因素。它似乎不仅消除了肿瘤侵袭的重要障碍,也消除了肿瘤增殖的重要障碍。