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首页> 外文期刊>European spine journal >Transcript levels of major MMPs and ADAMTS-4 in relation to the clinicopathological profile of patients with lumbar disc herniation
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Transcript levels of major MMPs and ADAMTS-4 in relation to the clinicopathological profile of patients with lumbar disc herniation

机译:腰椎间盘突出症患者主要MMP和ADAMTS-4的转录水平与临床病理特征的关系

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The involvement of matrix metalloproteinases (MMPs) in both the pathogenesis of intervertebral disc (ID) herniation and the spontaneous regression of herniated ID fragments remains only partially elucidated. The purpose of the present study was to simultaneously examine the transcript levels of a large number of MMPs (-1, -3, -8, -9, -13 and -14) and ADAMTS-4 (a disintegrin and metalloproteinase with thrombospondin motifs) and to investigate their correlation with the clinicopathologic profile of patients suffering from symptomatic lumbar ID herniation. mRNA expression levels were determined by means of the real-time polymerase chain reaction in 63 herniated and 10 control ID specimens. Our results showed multiple positive correlations among all MMPs and ADAMTS-4 mRNA in herniated samples, indicating their possible synergistic effect in ID herniation. MMP-9 and -13 mRNA levels were significantly elevated in patients with chronic pain, presumably as a consequence of neovascularization and chronic inflammation. Smoking habits were found to have a negative dose-dependent effect on the transcript levels of MMP-3 and MMP-13 and a positive correlation with pain intensity, suggesting an unfavorable role for smoking in the regression process of herniated disc fragments. Our findings provide evidence of the molecular portrait of MMPs and ADAMTS-4 in lumbar ID herniation, as well as of its association with the clinicopathological profile of the patients included in this study, reinforcing the hypothesis of MMPs involvement in the natural history of ID herniation. However, further studies are necessary to elucidate the exact role of MMPs in the resorption process of herniated lumbar discs...
机译:基质金属蛋白酶(MMPs)参与椎间盘(ID)突出的发病机制和突出的ID片段的自发消退的参与仍部分阐明。本研究的目的是同时检查大量MMP(-1,-3,-8,-9,-13和-14)和ADAMTS-4(具有血小板反应蛋白基序的整合素和金属蛋白酶)的转录水平)并研究其与有症状腰椎ID疝患者的临床病理特征的相关性。通过实时聚合酶链反应在63个突出的和10个对照ID标本中确定mRNA表达水平。我们的结果显示,所有MMP和ADAMTS-4 mRNA在椎间盘突出症样本中存在多个正相关,表明它们在ID椎间盘突出症中可能具有协同作用。慢性疼痛患者的MMP-9和-13 mRNA水平显着升高,可能是由于新生血管形成和慢性炎症所致。发现吸烟习惯对MMP-3和MMP-13的转录水平具有负剂量依赖性,并且与疼痛强度呈正相关,这表明吸烟在椎间盘突出的消退过程中起不利作用。我们的发现提供了腰椎ID疝中MMPs和ADAMTS-4的分子画像,以及与本研究中患者的临床病理特征相关的证据,从而加强了MMPs参与ID疝自然史的假设。 。但是,有必要进行进一步的研究以阐明MMP在腰椎间盘突出吸收过程中的确切作用...

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