巴尔干地方性肾病患者上路尿路癌中发现的微rna干扰和马兜铃酸中毒的分子特征:对当前文献的系统回顾。

IF 0.5 4区 医学 Q4 GENETICS & HEREDITY
D Bašić, I Ignjatović, Lj Janković Veličković, A Veljković
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引用次数: 0

摘要

术语“马兜铃酸肾病”(AAN)用于包括任何形式的中毒性间质性肾病,由摄入含有马兜铃酸(AA)的植物或由食物中的环境污染物(如巴尔干地方性肾病(BEN))引起。马兜铃酸(AA)中毒与上尿路上皮癌(UTUC)的发展密切相关;然而,潜在的分子机制仍有待确定。MicroRNAs (miRNA)调节多种生物过程,包括细胞增殖、分化和代谢,作为致癌基因或肿瘤抑制因子。独特的miRNA表达谱表明,miRNA可能在UTUC发育过程中起调节作用。本综述旨在总结有关AA-UTUC BEN患者mirna表达的潜在分子机制的文献资料。强相关性AA-UTUC具有独特的基因改变模式,AL-DNA加合物和独特的肿瘤蛋白(TP53)突变谱AAG到TAG (a: T→T: a)外显子第5位密码子139 (Lys→Stop)的翻转激活p53肿瘤抑制蛋白。此外,p53蛋白不仅负责mirna的表达,还作为mirna的靶分子,通过激活细胞周期蛋白依赖性激酶(CyclinD1)和细胞周期蛋白激酶6(CDK6)来支持细胞周期阻滞,在AA-UTUC致癌性中起着至关重要的作用。本研究提出了一种分子机制,代表了AA中毒、miRNAs表达和BEN患者UTUC进展之间可能存在的独特关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular Characterization of Microrna Interference and Aristolochic Acid Intoxication Found in Upper Tract Urothelial Carcinoma in Patients with Balkan Endemic Nephropathy: A Systematic Review of the Current Literature.

The term "aristolochic acid nephropathy" (AAN) is used to include any form of toxic interstitial nephropathy that is caused either by ingestion of plants containing aristolochic acids (AA) or by the environmental contaminants in food such as in Balkan endemic nephropathy (BEN). Aristolochic acid (AA) intoxication is strongly associated with the development of upper tract urothelial carcinoma (UTUC); however, the underlying molecular mechanism remains to be defined. MicroRNAs (miRNA) regulate several biological processes, including cell proliferation, differentiation, and metabolism, acting as oncogenes or tumor suppressors. A unique miRNA expression profile suggested that miRNAs could function as regulators in UTUC developmental processes. This review aimed to summarize data available in the literature about underlying molecular mechanisms leading to the expression of miRNAs in AA-UTUC patients with BEN. Strong correlation in AA-UTUC has a distinctive gene alteration pattern, AL-DNA adducts, and a unique tumor protein (TP53) mutational spectrum AAG to TAG (A: T→T: A) transversion in codon 139 (Lys → Stop) of exon 5 activates the p53 tumor suppressor protein. Further, p53 protein is responsible not only for the expression of miRNAs but also acts as a target molecule for miRNAs and plays a crucial function in the AA-UTUC pathogenicity through activation of cyclin-dependent kinase (CyclinD1) and cyclin protein kinase 6(CDK6) to support cell cycle arrest. This study, proposed a molecular mechanism that represented a possible unique relationship between AA intoxication, miRNAs expression, and the progression of UTUC in patients with BEN.

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来源期刊
CiteScore
1.00
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Balkan Journal of Medical Genetics is a journal in the English language for publication of articles involving all branches of medical genetics: human cytogenetics, molecular genetics, clinical genetics, immunogenetics, oncogenetics, pharmacogenetics, population genetics, genetic screening and diagnosis of monogenic and polygenic diseases, prenatal and preimplantation genetic diagnosis, genetic counselling, advances in treatment and prevention.
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