Next-generation tissue microarray (ngTMA) increases the quality of biomarker studies: an example using CD3, CD8, and CD45RO in the tumor microenvironment of six different solid tumor types
© Zlobec et al.; licensee BioMed Central Ltd. 2013
Received: 13 March 2013
Accepted: 23 April 2013
Published: 30 April 2013
Tissue microarray (TMA) technology revolutionized the investigation of potential biomarkers from paraffin-embedded tissues. However, conventional TMA construction is laborious, time-consuming and imprecise. Next-generation tissue microarrays (ngTMA) combine histological expertise with digital pathology and automated tissue microarraying. The aim of this study was to test the feasibility of ngTMA for the investigation of biomarkers within the tumor microenvironment (tumor center and invasion front) of six tumor types, using CD3, CD8 and CD45RO as an example.
Ten cases each of malignant melanoma, lung, breast, gastric, prostate and colorectal cancers were reviewed. The most representative H&E slide was scanned and uploaded onto a digital slide management platform. Slides were viewed and seven TMA annotations of 1 mm in diameter were placed directly onto the digital slide. Different colors were used to identify the exact regions in normal tissue (n = 1), tumor center (n = 2), tumor front (n = 2), and tumor microenvironment at invasion front (n = 2) for subsequent punching. Donor blocks were loaded into an automated tissue microarrayer. Images of the donor block were superimposed with annotated digital slides. Exact annotated regions were punched out of each donor block and transferred into a TMA block. 420 tissue cores created two ngTMA blocks. H&E staining and immunohistochemistry for CD3, CD8 and CD45RO were performed.
All 60 slides were scanned automatically (total time < 10 hours), uploaded and viewed. Annotation time was 1 hour. The 60 donor blocks were loaded into the tissue microarrayer, simultaneously. Alignment of donor block images and digital slides was possible in less than 2 minutes/case. Automated punching of tissue cores and transfer took 12 seconds/core. Total ngTMA construction time was 1.4 hours. Stains for H&E and CD3, CD8 and CD45RO highlighted the precision with which ngTMA could capture regions of tumor-stroma interaction of each cancer and the T-lymphocytic immune reaction within the tumor microenvironment.
Based on a manual selection criteria, ngTMA is able to precisely capture histological zones or cell types of interest in a precise and accurate way, aiding the pathological study of the tumor microenvironment. This approach would be advantageous for visualizing proteins, DNA, mRNA and microRNAs in specific cell types using in situ hybridization techniques.
KeywordsTissue microarray Next-generation Tumor microenvironment Automation Pathology
In the late 1990s, tissue microarray (TMA) technology revolutionized the investigation of potential prognostic and predictive biomarkers . TMAs involve the transfer of small tissue cores, typically 0.6 mm in diameter, from formalin-fixed paraffin-embedded (FFPE) tissues into an empty paraffin block . This repeated transfer of tissue cores leads to the construction of a “tissue-archive” that can contain hundreds of tissue samples from a small or large number of patients. TMAs can be used to study tissue morphology, expression of proteins or genes and chromosomal aberrations using different stains, immunohistochemistry and in situ hybridization [3–5]. The combination of TMAs and clinically annotated samples represents an elegant and cost-effective approach to study panels of biomarkers under identical experimental conditions and to develop prognostic or predictive models of patient outcomes .
Despite these considerable advantages, conventional construction of TMAs is not without its limitations. TMA construction is often described as a meticulous, laborious and time-consuming process. A major drawback lies in the “approximation” of desired tissue spots for transfer into the TMA. Before tissues can be punched out of their blocks, the corresponding hematoxylin and eosin (H&E) slides are reviewed. The histological areas of interest are then marked using a felt-tip pen directly on the slide. When various tissue types are present, different colors and marking of assorted sizes are made. Pathologists familiar with TMA construction will confirm that annotating “specific” regions of interest in this manner is challenging. The manual alignment of the annotated region from an H&E slide to the donating block is not always exact.
It is now recognized that tumor heterogeneity can have a significant impact on the interpretation of biomarkers . Increasingly important is the targeting of particular cell types, tissue types or histological zones using various core diameters of 0.6, 1.0, 1.5 or 2.0 mm. Traditional methods of tissue microarraying are suboptimal to achieve this goal; there is hence an urgent need to improve TMA technology to acquire histological precision, enhance the accuracy of punching and speed of construction. We have used the term next-generation TMAs (ngTMAs) to define the combination of cutting-edge digital pathology, automated tissue microarraying and histopathological expertise. The goal is to create TMAs containing the accurately determined histological structures with the aim of further optimizing biomarker research.
An example where ngTMAs would be useful is the investigation of the immune infiltrates in patients with different tumor types . In colorectal cancers, immunohistochemical panels of immune infiltrates such as CD3, CD8 and CD45RO have been investigated in the tumor microenvironment within the main tumor body as well as at the invasion front.
The aim of this study was to determine the feasibility of ngTMAs to investigate biomarkers at the tumor-stroma interface within the main tumor body and invasion front of six tumor types: malignant melanomas, as well as lung, prostate, gastric, colon and breast cancers, using T-cell markers CD3, CD8 and CD45RO as an example.
Materials and methods
In order to investigate the feasibility of ngTMAs for the assessment of host-related factors of the tumor microenvironment, six of the most frequently diagnosed tumor types were selected. Sixty cases were retrieved from the archives of the Institute of Pathology, University of Bern from 2009–2011 including 10 cases each of lung cancer, breast cancer, prostate cancer, gastric cancer, malignant melanoma and colon cancer. The diagnostic H&E slides were reviewed and the most representative one concerning the tumor microenvironment was selected for subsequent scanning. The use of patient material has been approved by the ethics committee of the Bern University Hospital (16-03-12).
Slide scanning and annotation
The selected H&E slide of each whole tissue section was placed into a scanning cartridge and loaded into the slide scanner (Pannoramic P250, 3DHistech). All 60 slides could be processed in a single run. Digital images were uploaded onto the digital slide management platform Case Center (http://ngtma.path.unibe.ch/casecenter). Each slide could then be opened and viewed using Pannoramic Viewer software (3DHistech).
Automated tissue microarraying
The 60 donor blocks corresponding to the 60 annotated digital slides were loaded into the automated tissue microarrayer (Grandmaster, 3DHistech) and an image of each block was taken. Two empty paraffin embedded recipient blocks were simultaneously loaded. A tissue microarray layout was created to design a punching-schema for the final tissue microarray block. The created layout consisted of 243 tissue punches at 1 mm in diameter, suggesting that 2 ngTMA blocks would be sufficient for this study.
With the Grandmaster software, each digital slide could be retrieved from the Case Center. Using tissue landmarks, the image of the donor block and the digital slide were superimposed for exact correspondence. Annotations could then be viewed and confirmed. Punching of the donor blocks and transfer into the recipient block could be made after confirmation of each annotation and occurred in the sequence arranged with the layout. The result was 2 ngTMAs, the first containing tissue cores of lung, stomach, colon and breast and the second containing additional spots of breast, malignant melanoma and prostate tissues.
The two ngTMAs were sectioned at 4 μm. After de-paraffination and rehydration, standard H&E staining was undertaken. In order to visualize the host-related immune markers, immunohistochemistry for the following antibodies was performed using an automated immunostainer (Leica, Bond III): Anti-CD3 (Abcam, clone SP7, tris buffer, 95° 30 minutes, 1:400), anti-CD8 (Dako, clone C8/144B, Tris buffer, 95° 20 minutes, 1:100) and anti-CD45RO (Abcam, clone UCH-L1, citrate buffer, 100° 30 minutes, 1:4000).
Slide scanning and annotation
All 60 slides could be loaded and scanned automatically overnight. The time required for each scan varied in accordance with the size of the whole tissue section and ranged from 5 to 12 minutes. Total scanning time was approximately 10 hours. Slides were directly uploaded to the correct folder in the Case Center. Digital slide annotation could be easily and rapidly performed in 1 minute, on average. Therefore, 7 annotations on 60 cases could be performed within 1 hour.
Automated tissue microarraying
The maximum capacity of the Grandmaster arrayer is 60 donor blocks therefore all selected blocks could be uploaded simultaneously. Land marking of donor block images and correspondence with digital slides was possible in less than 2 minutes per case followed by confirmation of annotated regions. Automated punching of tissue cores and transfer to the recipient block took 12 second per core. Punching could either be performed after confirming all annotations or after each single confirmed annotation. Total time for creating the 2 ngTMAs containing 420 cores at 1 mm in diameter was 1.4 hours.
Less than 2% of all tissue cores were unsuccessfully transferred from the donor block to the recipient block. These cores could however be recuperated in a second attempt resulting in a 100% successful transfer rate.
The tumor microenvironment is captured using ngTMA
Evaluation of the tumor microenvironment: host-related features
Planning and design
Based on scientific hypothesis and requirements, an interdisciplinary research task force should consider statistical issues such as sample size and the number of tissue punches per patient depending on the tumor types and especially from which tumor location. This step should be considered the “strategic level” of ngTMA and should not be under-estimated to avoid waste of time, material, human and financial resources; fast scanning and user friendly digital platform: these steps allow the visualization of slides using a digital platform which is the interface between all research groups involved and allows the discussion of cases without the need for additional meetings that are often logistically difficult to organize; precise annotations: this step is likely the most crucial as it requires experience in morphology to exactly determine the tumor locations from which the tissue punches should be taken from. In colorectal cancer, for example, a well-constructed ngTMA should include punches from normal tissue, tumor center, tumor front, intra-tumoral and peri-tumoral microenvironment and if available preoperative biopsies, lymph nodes or distant metastases. Differentiating these various histological “zones” may be challenging to the untrained eye and hence, an optimal ngTMA would be constructed in collaboration with pathologists; automated punching: this step facilitates the working process by its precision and flexibility; the choice of the core size depends on the scientific hypothesis; more “functional” ngTMAs such as one investigating epithelial-mesenchymal transition (EMT) may require a smaller sample size but larger tissue cores areas (1.5-2.0 mm in diameter), whereas more high-throughput studies could be performed using the “traditional” 0.6 mm punch size. In our experience using a conventional arrayer, an average of 15 cores can be punched and transferred per hour. Donor block punching and transfer to the recipient block took 12 seconds per core, thus significantly reducing the time and human resources necessary for TMA construction.
In the present analysis we tested whether the new approach of “ngTMA” could be an ideal platform to study the tumor microenvironment of different solid tumors. Indeed, the selected immune markers CD3, CD8 and CD45RO which are proposed as important prognostic immune infiltrates in the literature  could be visualized by immunohistochemistry in precisely targeted tissue punches from the microenvironment of the tumor center and the tumor invasive front. This approach may even become more important in the future when not only proteins, but also mRNA and microRNA can be visualized on paraffin embedded tissues using in situ hybridization techniques.
The authors would like to thank Guido Suter, Clinical Manager for his continued dedication and advice on this project and Mary Economou, Caroline Hammer and Dominique Müller for excellent technical support.
- Kallioniemi OP, Wagner U, Kononen J, Sauter G: Tissue microarray technology for high-throughput molecular profiling of cancer. Hum Mol Genet. 2001, 10: 657-10.1093/hmg/10.7.657.View ArticlePubMedGoogle Scholar
- Voduc D, Kenney C, Nielsen TO: Tissue microarrays in clinical oncology. Semin Radiat Oncol. 2008, 18: 89-10.1016/j.semradonc.2007.10.006.PubMed CentralView ArticlePubMedGoogle Scholar
- Fleischmann A, Rotzer D, Seiler R, Studer UE, Thalmann GN: Her2 amplification is significantly more frequent in lymph node metastases from urothelial bladder cancer than in the primary tumours. Eur Urol. 2011, 60: 350-10.1016/j.eururo.2011.05.035.View ArticlePubMedGoogle Scholar
- Tapia C: HER2 analysis in breast cancer: reduced immunoreactivity in FISH non-informative cancer biopsies. Int J Oncol. 2004, 25: 1551-PubMedGoogle Scholar
- Zlobec I: Node-negative colorectal cancer at high risk of distant metastasis identified by combined analysis of lymph node status, vascular invasion, and Raf-1 kinase inhibitor protein expression. Clin Cancer Res. 2008, 14: 143-10.1158/1078-0432.CCR-07-1380.View ArticlePubMedGoogle Scholar
- Zlobec I: Role of RHAMM within the hierarchy of well-established prognostic factors in colorectal cancer. Gut. 2008, 57: 1413-10.1136/gut.2007.141192.View ArticlePubMedGoogle Scholar
- Rehemtulla A: Overcoming intratumor heterogeneity of polygenic cancer drug resistance with improved biomarker integration. Neoplasia. 2012, 14: 1278-PubMed CentralView ArticlePubMedGoogle Scholar
- Galon J: Cancer classification using the Immunoscore: a worldwide task force. J Transl Med. 2012, 10: 205-10.1186/1479-5876-10-205.PubMed CentralView ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.