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基于粗针活检构建组织微阵列——一项系统文献综述

Construction of tissue microarrays from core needle biopsies - a systematic literature review.

作者信息

Albanghali Mohammad, Green Andrew, Rakha Emad, Aleskandarany Mohamed, Nolan Chris, Ellis Ian, Cheung Kwok-Leung

机构信息

Division of Medical Sciences and Graduate Entry Medicine, School of Medicine, University of Nottingham, Royal Derby Hospital Centre, Derby, UK.

Division of Cancer and Stem Cells, School of Medicine, University of Nottingham, Nottingham, UK.

出版信息

Histopathology. 2016 Feb;68(3):323-32. doi: 10.1111/his.12802. Epub 2015 Oct 25.

Abstract

In some clinical circumstances, core needle biopsy (CNB) may be the only source of material from cancer tissue for diagnostic use. The volume of tissue available in a CNB is low, and opportunities for research use can therefore be limited. The tissue microarray (TMA) principle, if applied to the use of CNBs, could facilitate research studies in circumstances where CNB specimens are available. However, various challenges are expected in applying such a technique in CNBs, which has limited their use in research. We therefore conducted a systematic review of the literature on this subject. A systematic search was carried out with CINAHL, EMBASE, the Cochrane library, and MEDLINE, to identify studies that have primarily developed methods for constructing TMAs from CNBs. Eight studies were found to meet the inclusion criteria; six of these employed the vertical rearrangement technique, and two used multiple layers of biopsy tissue. Representation of the CNB was significantly influenced by the quantity of tumour cells present in the original biopsy and the degree of heterogeneity of biomarker expression. This review shows that technologies have been developed to enable construction of TMAs from CNBs. However, challenges remain to improve amplification and representation.

摘要

在某些临床情况下,粗针活检(CNB)可能是获取癌症组织用于诊断的唯一材料来源。CNB可获得的组织量较少,因此用于研究的机会可能有限。如果将组织微阵列(TMA)原理应用于CNB的使用,在有CNB标本的情况下可以促进研究。然而,在CNB中应用这种技术预计会面临各种挑战,这限制了其在研究中的应用。因此,我们对关于这个主题的文献进行了系统综述。使用CINAHL、EMBASE、Cochrane图书馆和MEDLINE进行了系统检索,以识别主要开发了从CNB构建TMA方法的研究。发现有八项研究符合纳入标准;其中六项采用了垂直重排技术,两项使用了多层活检组织。原始活检中存在的肿瘤细胞数量和生物标志物表达的异质性程度对CNB的代表性有显著影响。本综述表明,已经开发出了从CNB构建TMA的技术。然而,在提高扩增和代表性方面仍存在挑战。

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