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Matrix metalloproteinases (MMPs): Modern molecular markers of open-angle glaucoma diagnosis and therapy

机译:基质金属蛋白酶(MMPs):开角型青光眼诊断和治疗的现代分子标记

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Glaucoma is one of the most important civilization diseases and leads to irreversible blindness. In spite of many years of research, the causes of this disorder remain unclear. This disease is extremely difficult to diagnose because its primary phase is asymptomatic. After laborious research it has been discovered that metalloproteinases, i.e. proteolytic enzymes involved in the pathogenesis of many kinds of glaucoma, are crucial in glaucoma diagnosis. The overexpression of matrixins leads to degradation of extracellular matrix components, which results in eye tissue injury and changes of tissue properties. Structural disorders occurring in this way are one of the many key reasons for progressive glaucomatous optic neuropathy. The presence of altered expressions of MMP-1, -2, -3, -7, -9, and -12 and their tissue inhibitors TIMP-1 and -2 in the glaucomatous eye paves new ways for the diagnosis and treatment of open-angle glaucoma. The detection of polymorphisms and mutations in genes encoding these enzymes will allow qualifying a patient to a risk group and people who are already ill may be treated by regulation of metalloproteinases activity. This review focuses on the presence and function of metalloproteinases in open-angle glaucoma and on treatment possibilities through MMP regulation.
机译:青光眼是最重要的文明疾病之一,并导致不可逆转的失明。尽管进行了多年的研究,但尚不清楚这种疾病的病因。由于该疾病的主要症状是无症状的,因此很难诊断。经过艰苦的研究,已发现金属蛋白酶,即参与多种青光眼发病机理的蛋白水解酶,对青光眼的诊断至关重要。基质素的过表达导致细胞外基质成分的降解,这导致眼组织损伤和组织性质的改变。以这种方式发生的结构障碍是进行性青光眼性视神经病变的许多关键原因之一。 MMP-1,-2,-3,-7,-9和-12及其组织抑制剂TIMP-1和-2表达的改变在青光眼中的存在为开眼的诊断和治疗铺平了道路角性青光眼。对编码这些酶的基因的多态性和突变的检测将使患者有资格进入危险组,并且已经患病的人可以通过调节金属蛋白酶活性来治疗。这篇综述集中在开角型青光眼中金属蛋白酶的存在和功能以及通过MMP调节的治疗可能性。

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