Evidence map›Paper›PMID 27600223›Full record

ArticleMicroarrays (Basel, Switzerland)2015

Re-Punching Tissue Microarrays Is Possible: Why Can This Be Useful and How to Do It.

Aurélien Lacombe, Vincenza Carafa, Sandra Schneider, Melanie Sticker-Jantscheff, Luigi Tornillo, Serenella Eppenberger-Castori

Abstract read
In one paragraph

Article in Microarrays (Basel, Switzerland), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Aurélien LacombeMolecular Pathology Division, Institute of Pathology, University Hospital of Basel, CH-4031 Basel, Switzerland. aurelien.lacombe@usb.ch.
Vincenza CarafaMolecular Pathology Division, Institute of Pathology, University Hospital of Basel, CH-4031 Basel, Switzerland. vincenza.carafa@usb.ch.
Sandra SchneiderMolecular Pathology Division, Institute of Pathology, University Hospital of Basel, CH-4031 Basel, Switzerland. sandra.schneider@usb.ch.
Melanie Sticker-JantscheffMolecular Pathology Division, Institute of Pathology, University Hospital of Basel, CH-4031 Basel, Switzerland. melanie.sticker@usb.ch.
Luigi TornilloMolecular Pathology Division, Institute of Pathology, University Hospital of Basel, CH-4031 Basel, Switzerland. luigi.tornillo@unibas.ch.
Serenella Eppenberger-CastoriMolecular Pathology Division, Institute of Pathology, University Hospital of Basel, CH-4031 Basel, Switzerland. sere.eppenberger@unibas.ch.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tissue microarray (TMA) methodology allows the concomitant analysis of hundreds of tissue specimens arrayed in the same manner on a recipient block. Subsequently, all samples can be processed under identical conditions, such as antigen retrieval procedure, reagent concentrations, incubation times with antibodies/probes, and escaping the inter-assays variability. Therefore, the use of TMA has revolutionized histopathology translational research projects and has become a tool very often used for putative biomarker investigations. TMAs are particularly relevant for large scale analysis of a defined disease entity. In the course of these exploratory studies, rare subpopulations can be discovered or identified. This can refer to subsets of patients with more particular phenotypic or genotypic disease with low incidence or to patients receiving a particular treatment. Such rare cohorts should be collected for more specific investigations at a later time, when, possibly, more samples of a rare identity will be available as well as more knowledge derived from concomitant, e.g., genetic, investigations will have been acquired. In this article we analyze for the first time the limits and opportunities to construct new TMA blocks using tissues from older available arrays and supplementary donor blocks. In summary, we describe the reasons and technical details for the construction of rare disease entities arrays.

Indexed as

EFFPEH&ampIHCROITMATMA-GMTMA-M

Identifiers

PMID27600223
PMCPMC4996397

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.