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Updated: Mar 26, 2026

A Next-generation Tissue Microarray ngTMA Protocol for Biomarker Studies
Published on: September 23, 2014
Tissue microarray use for immunohistochemical study of ameloblastoma.
Rodrigo Neves-Silva1, Felipe Paiva Fonseca1, Adriana Souza de Jesus2
1Oral Diagnosis Department, Semiology and Pathology, Piracicaba Dental School, University of Campinas (UNICAMP), Piracicaba, São Paulo, Brazil.
Tissue microarrays (TMA) are validated for ameloblastoma research. A 1.0-mm core in duplicate offers a reliable method for immunohistochemical studies of ameloblastoma.
Area of Science:
- Oral pathology
- Oncology
- Molecular biology
Background:
- Ameloblastoma is an aggressive odontogenic tumor known for high recurrence rates.
- Understanding ameloblastoma's molecular mechanisms is crucial for improved treatment strategies.
- Tissue microarray (TMA) is a high-throughput technique with potential for ameloblastoma research, but requires validation.
Purpose of the Study:
- To validate the use of TMA for immunohistochemical analysis of ameloblastoma.
- To determine the optimal TMA design for ameloblastoma studies.
Main Methods:
- Forty ameloblastoma cases were used to create TMA blocks with 1.0-mm and 2.0-mm cores, assembled in triplicate.
- Immunohistochemistry was performed for cytokeratins 14 and 19, Bcl-2, and Ki-67.
- TMA results were compared with conventional whole-section slides (CWSS) using semiquantitative analysis.
Main Results:
- Both 1.0-mm and 2.0-mm cores showed significant correlation with CWSS, particularly for Ki-67 and CK19.
- No significant differences were observed between core sizes or between duplicate and triplicate arrangements.
- 1.0-mm TMA cores exhibited a higher rate of core loss (33.74%) compared to 2.0-mm cores (4.99%).
Conclusions:
- Manual arrayer-based 1.0-mm TMA in duplicate is a valid and effective method for ameloblastoma immunohistochemical studies.
- This method demonstrates satisfactory agreement between TMA cores and CWSS.
- TMA provides a reliable approach for investigating the molecular characteristics of ameloblastoma.
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