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子宫平滑肌肉瘤的分子见解:系统评价。

Molecular Insights in Uterine Leiomyosarcoma: A Systematic Review.

机构信息

Clinic for Gynecology and Obstetrics, University Clinical Centre of Serbia, Koste Todorovića 26, 11000 Belgrade, Serbia.

Faculty of Medicine, University of Belgrade, 11000 Belgrade, Serbia.

出版信息

Int J Mol Sci. 2022 Aug 27;23(17):9728. doi: 10.3390/ijms23179728.

Abstract

Uterine fibroids (UFs) are the most common benign tumors of female genital diseases, unlike uterine leiomyosarcoma (LMS), a rare and aggressive uterine cancer. This narrative review aims to discuss the biology and diagnosis of LMS and, at the same time, their differential diagnosis, in order to distinguish the biological and molecular origins. The authors performed a Medline and PubMed search for the years 1990-2022 using a combination of keywords on the topics to highlight the many genes and proteins involved in the pathogenesis of LMS. The mutation of these genes, in addition to the altered expression and functions of their enzymes, are potentially biomarkers of uterine LMS. Thus, the use of this molecular and protein information could favor differential diagnosis and personalized therapy based on the molecular characteristics of LMS tissue, leading to timely diagnoses and potential better outcomes for patients.

摘要

子宫肌瘤(UFs)是女性生殖系统最常见的良性肿瘤,而不同于子宫平滑肌肉瘤(LMS),它是一种罕见且侵袭性的子宫癌。本叙述性综述旨在讨论 LMS 的生物学和诊断,并同时讨论其鉴别诊断,以区分其生物学和分子起源。作者使用 Medline 和 PubMed 在 1990 年至 2022 年间进行了搜索,使用了关于这些主题的关键词组合,以突出涉及 LMS 发病机制的许多基因和蛋白质。这些基因的突变,除了其酶的表达和功能改变外,都是子宫 LMS 的潜在生物标志物。因此,使用这种分子和蛋白质信息可以有利于基于 LMS 组织的分子特征进行鉴别诊断和个体化治疗,从而为患者及时诊断和潜在更好的治疗结果提供帮助。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6520/9456512/99fa74e916fa/ijms-23-09728-g001.jpg

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