Department of Pathology, New York University Medical Center, New York, NY, USA.
J Clin Pathol. 2013 Jul;66(7):627-9. doi: 10.1136/jclinpath-2012-201171. Epub 2013 Mar 9.
To develop and validate a technique for construction of intermediate density tissue microarray (TMA) slides based on the transfer of tissue from pre-existing routine slides provided for pathology diagnosis with validation to show preservation of morphology and antigenicity of the transferred tissue.
Prostate cancer patch TMAs were constructed using 20 cores acquired from radical prostatectomy histology slides. The preservation of morphology and antigenicity of these patch TMAs were tested with immunohistochemistry (IHC) in comparison to a traditional TMA.
After IHC staining, 35 of 39 cores (89.7%) on the patch TMA were intact compared with 39 of 40 cores (97.5%) on the traditional TMA. Expression patterns and density of the antigens (34BE12, p63 and AMACR) on the patch TMA were almost identical to the traditional TMA.
Patch TMA represents a viable alternative for tissue-based IHC studies when paraffin blocks are unavailable. This may be a valuable tool for allowing use of archival slide material for IHC and enable a standardized TMA platform to be used when the slides sent for review from other institutions are the only source of tissue available.
开发并验证一种基于转移病理诊断用常规切片组织的中间密度组织微阵列(TMA)载片的构建技术,验证其组织形态和抗原性保持情况。
使用从根治性前列腺切除术组织学切片获得的 20 个核心构建前列腺癌组织微阵列。通过免疫组织化学(IHC)比较传统 TMA 对这些组织微阵列的形态和抗原性进行检测。
免疫组化染色后,与传统 TMA 相比,组织微阵列上的 39 个核心中有 35 个(89.7%)保持完整,而传统 TMA 中有 40 个核心中有 39 个(97.5%)保持完整。组织微阵列上的抗原(34BE12、p63 和 AMACR)的表达模式和密度与传统 TMA 几乎相同。
当无法获得石蜡块时,组织微阵列代表了一种可行的基于组织的 IHC 研究替代方法。这可能是一种有价值的工具,可以允许使用存档切片材料进行 IHC,并在其他机构发送的用于审查的切片是唯一可用组织来源时,使用标准化的 TMA 平台。