卵巢癌液体活检的新发现

Antoniadis Panagiotis, Gheorghe Florentina Alina, Nitu Madalina Ana Maria, Nitu Cezara Gabriela, Constantinescu Diana Roxana, Duica Florentina
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摘要

通过新的分析技术的发展,许多关于肿瘤疾病方法的问题已经得到阐明。随着近年来分析方法的发展,各种组学技术已经发展到可以在不同时间在癌症患者的血液中评估肿瘤细胞和产物的特征。卵巢癌(OC)是最难诊断的肿瘤之一,由于这些疾病的高度异质性,在病因和分子特征方面是不同的,但它们只是共享一个解剖外观,生存率很低。最近的研究结果表明,分类为不同组织型的几种类型的卵巢癌实际上源于非卵巢问题,并且几乎没有分子相似性。在此背景下,卵巢癌的筛查和诊断可以通过使用液体活检技术评估外周血循环肿瘤细胞来进行。液体活检分析的各种分子的研究进展表明,肿瘤内和肿瘤间异质性以及肿瘤的时空演变可以通过一系列血液检查而不是通过对原发肿瘤组织样本的组织病理学分析来追踪。因此,利用液体活检对循环肿瘤细胞(CTC)、循环肿瘤DNA (ctDNA)、循环无细胞RNA(非编码和mRNA、细胞外囊泡)、肿瘤诱导血小板或不同mirna等分子进行评估,可以改善患者的管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
New insights of liquid biopsy in ovarian cancer
Through the development of new analysis technologies, many issues regarding the approach to tumoral diseases have been elucidated. With analytical assays developed in the last years, various omics technologies have evolved in such a manner that the characteristics of tumor cells and products can be evaluated (assessed) in the bloodstream of cancer patients at different times. Ovarian Cancer (OC) is one of the most difficult to diagnose umors, with low survival rates due to the high heterogeneity of these diseases that are distinct in terms of etiology and molecular characteristics, but which simply share an anatomical appearance. Recent findings have indicated that several types of ovarian cancer classified into different histotypes are in fact derived from non-ovarian issues and share few molecular similarities. Within this context, ovarian cancer screening and diagnosis can be made through the evaluation of circulating tumor cells in peripheral blood using liquid biopsy technologies. Advances in the study of various molecules analyzed by liquid biopsy have shown that elucidation of intratumoural and intertumoural heterogeneity and spatial and temporal tumor evolution could be traced by serial blood tests rather than by histopathological analyses of tissue samples from a primary tumor. Therefore, evaluation of some molecules such as circulating tumor cells (CTC), circulating tumor DNA (ctDNA), circulating cell-free RNA (non-coding and mRNA, extracellular vesicles), tumor-educated platelets or different miRNAs using liquid biopsy could lead to improvement of patient management.
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