The Good and the Bad of SHROOM3 in Kidney Development and Disease: A Narrative Review.

IF 1.6 Q3 UROLOGY & NEPHROLOGY Canadian Journal of Kidney Health and Disease Pub Date : 2023-12-13 eCollection Date: 2023-01-01 DOI:10.1177/20543581231212038
Amy Paul, Allison Lawlor, Kristina Cunanan, Pukhraj S Gaheer, Aditya Kalra, Melody Napoleone, Matthew B Lanktree, Darren Bridgewater
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Abstract

Purpose of review: Multiple large-scale genome-wide association meta-analyses studies have reliably identified an association between genetic variants within the SHROOM3 gene and chronic kidney disease. This association extends to alterations in known markers of kidney disease including baseline estimated glomerular filtration rate, urinary albumin-to-creatinine ratio, and blood urea nitrogen. Yet, an understanding of the molecular mechanisms behind the association of SHROOM3 and kidney disease remains poorly communicated. We conducted a narrative review to summarize the current state of literature regarding the genetic and molecular relationships between SHROOM3 and kidney development and disease.

Sources of information: PubMed, PubMed Central, SCOPUS, and Web of Science databases, as well as review of references from relevant studies and independent Google Scholar searches to fill gaps in knowledge.

Methods: A comprehensive narrative review was conducted to explore the molecular mechanisms underlying SHROOM3 and kidney development, function, and disease.

Key findings: SHROOM3 is a unique protein, as it is the only member of the SHROOM group of proteins that regulates actin dynamics through apical constriction and apicobasal cell elongation. It holds a dichotomous role in the kidney, as subtle alterations in SHROOM3 expression and function can be both pathological and protective toward kidney disease. Genome-wide association studies have identified genetic variants near the transcription start site of the SHROOM3 gene associated with chronic kidney disease. SHROOM3 also appears to protect the glomerular structure and function in conditions such as focal segmental glomerulosclerosis. However, little is known about the exact mechanisms by which this protection occurs, which is why SHROOM3 binding partners remain an opportunity for further investigation.

Limitations: Our search was limited to English articles. No structured assessment of study quality was performed, and selection bias of included articles may have occurred. As we discuss future directions and opportunities, this narrative review reflects the academic views of the authors.

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SHROOM3 在肾脏发育和疾病中的利弊:叙述性综述。
综述目的:多项大规模全基因组关联荟萃分析研究可靠地确定了 SHROOM3 基因内的遗传变异与慢性肾病之间的关联。这种关联还延伸到已知肾脏疾病标志物的改变,包括基线估计肾小球滤过率、尿白蛋白与肌酐比率和血尿素氮。然而,人们对 SHROOM3 与肾脏疾病相关的分子机制的了解仍然很少。我们进行了一项叙述性综述,总结了有关 SHROOM3 与肾脏发育和疾病之间的遗传和分子关系的文献现状:信息来源:PubMed、PubMed Central、SCOPUS 和 Web of Science 数据库,以及相关研究的参考文献和独立的 Google Scholar 搜索,以填补知识空白:对 SHROOM3 与肾脏发育、功能和疾病的分子机制进行了全面的叙述性综述:SHROOM3是一种独特的蛋白质,因为它是SHROOM组蛋白质中唯一通过顶端收缩和顶端基底细胞伸长调节肌动蛋白动力学的成员。它在肾脏中扮演着双重角色,因为 SHROOM3 表达和功能的微妙变化既可能是病理变化,也可能对肾脏疾病具有保护作用。全基因组关联研究发现,SHROOM3 基因转录起始位点附近的遗传变异与慢性肾病有关。在局灶节段性肾小球硬化症等情况下,SHROOM3 似乎还能保护肾小球的结构和功能。然而,人们对这种保护的确切机制知之甚少,这就是为什么SHROOM3的结合伙伴仍是进一步研究的机会:我们的搜索仅限于英文文章。局限性:我们的搜索仅限于英文文章,没有对研究质量进行结构化评估,因此可能存在对纳入文章的选择偏差。当我们讨论未来的方向和机遇时,这篇叙述性综述反映了作者的学术观点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.00
自引率
5.90%
发文量
84
审稿时长
12 weeks
期刊介绍: Canadian Journal of Kidney Health and Disease, the official journal of the Canadian Society of Nephrology, is an open access, peer-reviewed online journal that encourages high quality submissions focused on clinical, translational and health services delivery research in the field of chronic kidney disease, dialysis, kidney transplantation and organ donation. Our mandate is to promote and advocate for kidney health as it impacts national and international communities. Basic science, translational studies and clinical studies will be peer reviewed and processed by an Editorial Board comprised of geographically diverse Canadian and international nephrologists, internists and allied health professionals; this Editorial Board is mandated to ensure highest quality publications.
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