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基因表达在压力性尿失禁中的作用:证据的综合评价。

The Role of Gene Expression in Stress Urinary Incontinence: An Integrative Review of Evidence.

机构信息

Department of Gynecology and Obstetrics, University Hospital Centre, 10 000 Zagreb, Croatia.

Medical School, University of Zagreb, 10 000 Zagreb, Croatia.

出版信息

Medicina (Kaunas). 2023 Apr 3;59(4):700. doi: 10.3390/medicina59040700.

DOI:10.3390/medicina59040700
PMID:37109658
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10142382/
Abstract

Stress urinary incontinence (SUI) is defined as unintentional urine leakage occurring as a consequence of increased intraabdominal pressure due to absent or weak musculus detrusor contractility. It affects postmenopausal women more often than premenopausal and is associated with quality of life (QoL) deterioration. The complex SUI etiology is generally perceived as multifactorial; however, the overall impact of environmental and genetic influences is deficiently understood. In this research report, we have disclosed the upregulation of 15 genes and the downregulation of 2 genes in the genetic etiology of SUI according to the accessible scientific literature. The analytical methods used for the analysis of gene expression in the studies investigated were immunohistochemistry, immunofluorescence staining, PCR, and Western blot. In order to facilitate the interpretation of the results, we have used GeneMania, a potent software which describes genetic expression, co-expression, co-localization, and protein domain similarity. The importance of this review on the genetic pathophysiology of SUI lies in determining susceptibility for targeted genetic therapy, detecting clinical biomarkers, and other possible therapeutic advances. The prevention of SUI with the timely recognition of genetic factors may be important for avoiding invasive operative urogynecological methods.

摘要

压力性尿失禁(SUI)定义为由于腹内压增加而导致的无意识尿液泄漏,这是由于逼尿肌收缩力缺失或减弱引起的。它在绝经后妇女中比绝经前妇女更为常见,并且与生活质量(QoL)恶化有关。SUI 的复杂病因通常被认为是多因素的;然而,环境和遗传影响的总体影响理解不足。在本研究报告中,我们根据可获得的科学文献,揭示了 SUI 遗传病因中 15 个基因的上调和 2 个基因的下调。用于研究中基因表达分析的分析方法是免疫组织化学、免疫荧光染色、PCR 和 Western blot。为了便于解释结果,我们使用了 GeneMania,这是一种强大的软件,用于描述基因表达、共表达、共定位和蛋白质结构域相似性。本综述对 SUI 的遗传病理生理学的重要性在于确定靶向基因治疗的易感性,检测临床生物标志物和其他可能的治疗进展。通过及时识别遗传因素来预防 SUI 对于避免侵入性手术性妇科泌尿科方法可能很重要。

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本文引用的文献

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Macrophage Receptor With Collagenous Structure Polymorphism and Recurrent Respiratory Infections and Wheezing During Infancy: A 5-Years Follow-Up Study.具有胶原结构的巨噬细胞受体多态性与婴儿期反复呼吸道感染及喘息:一项5年随访研究
Front Pediatr. 2021 Jul 27;9:666423. doi: 10.3389/fped.2021.666423. eCollection 2021.
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Genome-Wide Association Study Identifies Two Novel Loci Associated with Female Stress and Urgency Urinary Incontinence.全基因组关联研究鉴定出与女性应激性和急迫性尿失禁相关的两个新位点。
J Urol. 2021 Sep;206(3):679-687. doi: 10.1097/JU.0000000000001822. Epub 2021 Apr 27.
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The PRISMA 2020 statement: an updated guideline for reporting systematic reviews.
PRISMA 2020 声明:系统评价报告的更新指南。
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High Expression of COL17A1 Predicts Poor Prognosis and Promotes the Tumor Progression via NF-B Pathway in Pancreatic Adenocarcinoma.COL17A1高表达预示胰腺癌预后不良并通过NF-κB途径促进肿瘤进展。
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Targeting STAT3 in Cancer Immunotherapy.靶向 STAT3 在癌症免疫治疗中的作用。
Mol Cancer. 2020 Sep 24;19(1):145. doi: 10.1186/s12943-020-01258-7.
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NHD2-15, a novel antagonist of Growth Factor Receptor-Bound Protein-2 (GRB2), inhibits leukemic proliferation.NHD2-15,一种生长因子受体结合蛋白-2(GRB2)的新型拮抗剂,可抑制白血病增殖。
PLoS One. 2020 Aug 11;15(8):e0236839. doi: 10.1371/journal.pone.0236839. eCollection 2020.
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ANO1 in urethral SMCs contributes to sex differences in urethral spontaneous tone.ANO1 在尿道平滑肌细胞中的表达导致了尿道自发张力的性别差异。
Am J Physiol Renal Physiol. 2020 Sep 1;319(3):F394-F402. doi: 10.1152/ajprenal.00174.2020. Epub 2020 Jul 20.
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J Pediatr Surg. 2020 Aug;55(8):1621-1625. doi: 10.1016/j.jpedsurg.2020.02.001. Epub 2020 Feb 11.
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