首页> 外文期刊>Otolaryngology--head and neck surgery: official journal of American Academy of Otolaryngology-Head and Neck Surgery >Role of membrane type 1-matrix metalloproteinase and gelatinase A in head and neck squamous cell carcinoma invasion in vitro.
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Role of membrane type 1-matrix metalloproteinase and gelatinase A in head and neck squamous cell carcinoma invasion in vitro.

机译:膜1型基质金属蛋白酶和明胶酶A在头颈部鳞状细胞癌体外侵袭中的作用。

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摘要

The proteolytic activity of gelatinase A, a member of the matrix metalloproteinase (MMP) family, is considered to be a critical factor in tumor cell penetration of the extracellular matrix. To express catalytic activity, however, gelatinase A requires activation by another MMP, membrane type 1-matrix metalloproteinase (MT1-MMP). The head and neck squamous cell carcinoma cell line, UM-SCC-1, forms a quiescent monolayer atop collagen unless stimulated with epidermal growth factor (EGF; 3.5 nmol/L), which induces single cell invasion within 48 hours. To determine the role of the MT1-MMP/gelatinase A protease system in an in vitro stromal invasion model, expression vectors for MT1-MMP and gelatinase A were transfected into UM-SCC-1 (SCC-1/MT and SCC-1/gelA, respectively). SCC-1/MT tumor cells were found to invade in the absence of growth factor stimulation. Additionally, these cells displayed shorter onset to invasion and penetrated deeper into the collagen gel with EGF stimulation than did control vector transfectants. SCC-1/gelA cells similarly demonstrated invasion in the absence of EGF and a heightened invasive potential under EGF-stimulated conditions. These results suggest that the MT1-MMP/gelatinase A protease system participates in squamous cell carcinoma invasion of collagenous matrices.
机译:明胶酶A(基质金属蛋白酶(MMP)家族的成员)的蛋白水解活性被认为是肿瘤细胞穿透细胞外基质的关键因素。但是,为了表达催化活性,明胶酶A需要被另一种MMP激活,即膜型1-基质金属蛋白酶(MT1-MMP)。除非经表皮生长因子(EGF; 3.5 nmol / L)刺激,头颈部鳞状细胞癌细胞系UM-SCC-1会在胶原蛋白顶上形成一个静止的单层,在48小时内诱导单细胞侵袭。为了确定MT1-MMP /明胶酶A蛋白酶系统在体外基质侵袭模型中的作用,将MT1-MMP和明胶酶A的表达载体转染到UM-SCC-1(SCC-1 / MT和SCC-1 / gelA)。发现在没有生长因子刺激的情况下,SCC-1 / MT肿瘤细胞会侵袭。另外,与对照载体转染子相比,这些细胞在EGF刺激下显示出更短的侵袭开始并且更深入地渗透到胶原凝胶中。 SCC-1 / gelA细胞在没有EGF的情况下同样表现出侵袭性,并且在EGF刺激的条件下具有更高的侵袭潜力。这些结果表明MT1-MMP /明胶酶A蛋白酶系统参与了胶原基质的鳞状细胞癌侵袭。

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