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腹主动脉瘤中血管生成和炎症关键调节因子的失调。

Dysregulations of Key Regulators of Angiogenesis and Inflammation in Abdominal Aortic Aneurysm.

机构信息

Chair and Department of Biology and Genetics, Medical University of Lublin, 4a Chodźki St., 20-093 Lublin, Poland.

Chair and Department of Vascular Surgery and Angiology, Medical University of Lublin, 11 Staszica St., 20-081 Lublin, Poland.

出版信息

Int J Mol Sci. 2023 Jul 28;24(15):12087. doi: 10.3390/ijms241512087.

Abstract

Abdominal aortic aneurysm (AAA) is a chronic vascular disease caused by localized weakening and broadening of the abdominal aorta. AAA is a clearly underdiagnosed disease and is burdened with a high mortality rate (65-85%) from AAA rupture. Studies indicate that abnormal regulation of angiogenesis and inflammation contributes to progression and onset of this disease; however, dysregulations in the molecular pathways associated with this disease are not yet fully explained. Therefore, in our study, we aimed to identify dysregulations in the key regulators of angiogenesis and inflammation in patients with AAA in peripheral blood mononuclear cells (using qPCR) and plasma samples (using ELISA). Expression levels of , , , , , and and plasma levels of TGF-alpha, TGF-beta 1, VEGF-A, and VEGF-C were found to be significantly altered in the AAA group compared to the control subjects without AAA. Associations between analyzed factors and risk factors or biochemical parameters were also explored. Any of the analyzed factors was associated with the size of the aneurysm. The presented study identified dysregulations in key angiogenesis- and inflammation-related factors potentially involved in AAA formation, giving new insight into the molecular pathways involved in the development of this disease and providing candidates for biomarkers that could serve as diagnostic or therapeutic targets.

摘要

腹主动脉瘤(AAA)是一种由腹主动脉局部弱化和扩张引起的慢性血管疾病。AAA 是一种明显诊断不足的疾病,AAA 破裂导致的死亡率很高(65-85%)。研究表明,血管生成和炎症的异常调节与该疾病的进展和发生有关;然而,与该疾病相关的分子途径的失调尚不完全清楚。因此,在我们的研究中,我们旨在通过 qPCR 检测外周血单核细胞和 ELISA 检测血浆样本,鉴定 AAA 患者中血管生成和炎症关键调节因子的失调。与无 AAA 的对照组相比,AAA 组中 、 、 、 、 和 的表达水平以及 TGF-α、TGF-β1、VEGF-A 和 VEGF-C 的血浆水平明显改变。还探讨了分析因素与危险因素或生化参数之间的关联。分析的任何因素都与动脉瘤的大小有关。本研究鉴定了与 AAA 形成相关的关键血管生成和炎症相关因子的失调,为该疾病发展过程中涉及的分子途径提供了新的见解,并为可能作为诊断或治疗靶点的生物标志物提供了候选物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/636c/10418409/a6f89f99778a/ijms-24-12087-g001.jpg

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