Department of Dermatology, People's Hospital of Zhengzhou, Zhengzhou, China.
J Dermatol. 2012 Apr;39(4):339-43. doi: 10.1111/j.1346-8138.2011.01441.x. Epub 2011 Dec 13.
Elevated heparanase and matrix metalloproteinase (MMP)-9, frequently found in human cancer, is a major cause of degradation of the extracellular matrix (ECM) and basement membrane (BM), thus facilitating tumor cell migration and invasion. Although a lot of work has been done, the role of heparanase and MMP-9 has not been delineated in skin cancer progression. The purpose of this study was to do such an exploration. To investigate the role of heparanase and MMP-9 in cutaneous malignant melanoma (CMM) development, we performed immunohistochemical analysis to detect the alternation of these two factors in paraffin-embedded biopsy specimens of normal skin, junctional nevi and CMM. It is interesting to note that the expression profile of heparanase and MMP-9 was similar. Contrary to negative staining in normal skin, overexpression of heparanase and cytoplasmic MMP-9 was observed in as many as 70% of CMM, whereas only 10% of the junctional nevi exhibited faint staining (P = 0.0005, P = 0.0000). Considering the lymph node (LN) metastasis, the expression of the two factors is significantly higher in LN-positive lesions than that in LN-negative lesions (P = 0.0295, P = 0.0013). Meanwhile, there was positive correlation between the expression of MMP-9 and heparanase (r = 0.689, P = 0.003). The first expression of MMP-9 and heparanase occurs at benign lesions. However, the significantly increased expression in advanced CMM stages, particularly in LN-positive metastasis lesions, might synergistically contribute to degradation of ECM and BM, therefore promoting carcinogenesis and metastasis.
肝素酶和基质金属蛋白酶(MMP)-9 水平升高常见于人类癌症,是细胞外基质(ECM)和基底膜(BM)降解的主要原因,从而促进肿瘤细胞迁移和侵袭。尽管已经做了很多工作,但肝素酶和 MMP-9 在皮肤癌进展中的作用尚未阐明。本研究旨在对此进行探讨。为了研究肝素酶和 MMP-9 在皮肤恶性黑色素瘤(CMM)发展中的作用,我们通过免疫组织化学分析检测了这两种因子在石蜡包埋活检标本中的变化,包括正常皮肤、交界痣和 CMM。有趣的是,肝素酶和 MMP-9 的表达谱相似。与正常皮肤的阴性染色相反,高达 70%的 CMM 中观察到肝素酶和细胞质 MMP-9 的过表达,而只有 10%的交界痣表现出微弱染色(P = 0.0005,P = 0.0000)。考虑到淋巴结(LN)转移,LN 阳性病变中两种因子的表达明显高于 LN 阴性病变(P = 0.0295,P = 0.0013)。同时,MMP-9 和肝素酶的表达之间存在正相关(r = 0.689,P = 0.003)。MMP-9 和肝素酶的首次表达发生在良性病变中。然而,在 CMM 晚期,尤其是在 LN 阳性转移病变中,表达显著增加,可能协同促进 ECM 和 BM 的降解,从而促进癌变和转移。