VEGF、YAP1和PTEN免疫染色在子痫前期的微阵列表达结果。

Ayhan Atigan, Yeliz Arman Karakaya, Derya Kiliç, Omer Tolga Guler
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引用次数: 0

摘要

我们的目的是评估YAP1、PTEN、VEGF在子痫前期患者胎盘和健康孕妇胎盘中滋养细胞侵袭的表达,这与癌症的发病机制相似。对70名分娩妇女的胎盘进行了评估,其中包括30名先兆子痫妇女和40名健康对照者。采用微阵列法对胎盘组织进行YAP1、PTEN、VEGF免疫组化染色。YAP1、PTEN和VEGF强度的平均值±标准差为;1.57±0.71,2.59±0.80,1.61±0.59,分别。子痫前期组PTEN强度明显低于对照组(2.37±0.99 vs 2.75±0.58,p = 0.049)。各组间YAP1、VEGF染色差异无统计学意义(p > 0.05)。先兆子痫的发病机制尚不清楚。然而,由于滋养细胞侵袭和内皮细胞修复与癌症机制具有相似的方面,因此子痫前期和癌症研究都是相互支持的。我们的研究是一个原型研究,表明通过使用微阵列方法作为经济模型,可以很容易地进行大规模参与研究。
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Microarray expression results of VEGF, YAP1 and PTEN immunostains in preeclampsia cases.

We aimed to evaluate the expression of YAP1, PTEN, VEGF in the placentas of patients with preeclampsia and placentas of healthy pregnant women for trophoblast invasion, which is similar to cancer etiopathogenesis. The placentas of 70 women who gave birth, including 30 preeclampsia and 40 healthy controls, were evaluated. YAP1, PTEN and VEGF immunohistochemical staining were performed using the microarray method on placental tissue. The mean ± standard deviation for YAP1, PTEN and VEGF intensity were; 1.57 ± 0.71,2.59 ± 0.80, 1.61 ± 0.59, respectively. PTEN intensity was statistically significantly lower in the preeclampsia group than in the control group (2.37 ± 0.99 vs 2.75 ± 0.58, p = .049). There was no difference between the groups in terms of YAP1 and VEGF staining (p > .05). The etiopathogenesis of preeclampsia is still unclear. However, since trophoblast invasion and endothelial repair have similar aspects with cancer mechanisms, both preeclampsia and cancer studies are progressing by supporting each other. Our study is a prototype study showing that large-participation studies can be carried out easily by using the microarray method as an economic model.

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来源期刊
CiteScore
3.50
自引率
0.00%
发文量
38
审稿时长
>12 weeks
期刊介绍: The Journal of Immunoassay & Immunochemistry is an international forum for rapid dissemination of research results and methodologies dealing with all aspects of immunoassay and immunochemistry, as well as selected aspects of immunology. They include receptor assay, enzyme-linked immunosorbent assay (ELISA) in all of its embodiments, ligand-based assays, biological markers of ligand-receptor interaction, in vivo and in vitro diagnostic reagents and techniques, diagnosis of AIDS, point-of-care testing, clinical immunology, antibody isolation and purification, and others.
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