The Assessment of CDX1, IHH, SHH, GATA4, FOXA2, FOXF1 in Congenital Intra-Abdominal Adhesions

Q3 Medicine
Helēna Freijere Pope, M. Pilmane, Anna Junga, A. Petersons
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Abstract

Congenital abdominal adhesions are a rare condition that can result in a small bowel obstruction at any age, more frequently in pediatric populations. The cause remains unknown, and the importance of aberrant congenital bands is related to the difficulty of diagnosis, and cases of death with late detection have been documented. This research examines the expression of Caudal Type Homeobox 1 (CDX1), Indian Hedgehog (IHH), Sonic Hedgehog (SHH), GATA Binding Protein 4 (GATA4), Forkhead Box A2 (FOXA2) and Forkhead Box F1 (FOXF1) gene expression in human abdominal congenital adhesion fibroblast and endothelium cells by chromogenic in situ hybridization, with the aim of elucidating their potential association with the etiology of congenital intra-abdominal adhesion band development. The potential genes’ signals were examined using a semi-quantitative approach. Significant correlations were observed between the expression of CDX1 (p <.001) and SHH (p=0.032) genes in fibroblasts from congenital intra-abdominal adhesions compared to fibroblasts from control peritoneal tissue. Statistically significant very strong correlations were found between the CDX1 and IHH comparing endothelium and fibroblast cells in congenital abdominal adhesion bands. There was no statistically significant difference found in the distribution of IHH, FOXA2, GATA4, and FOXF1 between the fibroblasts and endothelium of the patients compared to the control group. The presence of notable distinctions and diverse associations suggests the potential involvement of numerous morpho-pathogenetic processes in the development of intraabdominal adhesions.
CDX1、IHH、SHH、GATA4、FOXA2、FOXF1 对先天性腹腔内粘连的评估
先天性腹腔粘连是一种罕见的疾病,可导致任何年龄段的小肠梗阻,在儿科人群中更为常见。病因至今不明,先天性异常腹腔粘连的重要性与诊断的难度有关,有文献记载发现过晚导致死亡的病例。这项研究检测了尾状同源染色体 1(CDX1)、印度刺猬(IHH)、声刺猬(SHH)、GATA 结合蛋白 4(GATA4)的表达、通过显色原位杂交研究人腹腔先天性粘连成纤维细胞和内皮细胞中叉头盒 A2(FOXA2)和叉头盒 F1(FOXF1)基因的表达,旨在阐明它们与先天性腹腔内粘连带发育病因的潜在联系。采用半定量方法对潜在基因的信号进行了检测。与对照腹膜组织的成纤维细胞相比,先天性腹腔内粘连的成纤维细胞中 CDX1(p <.001)和 SHH(p=0.032)基因的表达存在显著相关性。先天性腹腔粘连带内皮细胞和成纤维细胞的 CDX1 和 IHH 比较发现,两者之间存在统计学意义上的非常强的相关性。与对照组相比,患者的成纤维细胞和内皮细胞中 IHH、FOXA2、GATA4 和 FOXF1 的分布无明显统计学差异。明显的差异和多种关联的存在表明,腹腔内粘连的发生可能与多种形态-病理过程有关。
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来源期刊
Acta Medica Lituanica
Acta Medica Lituanica Medicine-General Medicine
CiteScore
0.70
自引率
0.00%
发文量
33
审稿时长
16 weeks
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