Decline in Antigenicity of Tumor Markers by Storage Time Using Pathology Sections Cut From Tissue Microarrays
AuthorBlows, FM; Ali, HR; Dawson, S-J; Le Quesne, J; Provenzano, E; Caldas, C; Pharoah, PDP
Source TitleApplied Immunohistochemistry and Molecular Morphology
PublisherLIPPINCOTT WILLIAMS & WILKINS
University of Melbourne Author/sDawson, Sarah-Jane
AffiliationSir Peter MacCallum Department of Oncology
Document TypeJournal Article
CitationsBlows, F. M., Ali, H. R., Dawson, S. -J., Le Quesne, J., Provenzano, E., Caldas, C. & Pharoah, P. D. P. (2016). Decline in Antigenicity of Tumor Markers by Storage Time Using Pathology Sections Cut From Tissue Microarrays. APPLIED IMMUNOHISTOCHEMISTRY & MOLECULAR MORPHOLOGY, 24 (3), pp.221-226. https://doi.org/10.1097/PAI.0000000000000172.
Access StatusOpen Access
Sectioning a whole tissue microarrray (TMA block) and storing the sections maximizes the number of sections obtained, but may impair the antigenicity of the stored sections. We have investigated the impact of TMA section storage on antigenicity. First, we reexamined existing TMA data to determine whether antigenicity in stored sections changes over time. Component scores for each marker, based on cellular compartment of staining and score-type, were evaluated separately. Residual components scores adjusted for grade, tumor size, and node positivity, were regressed on the number of days storage to evaluate the effect of storage time. Storage time ranged from 2 to 1897 days, and the mean change in antigenicity per year ranged from -0.88 (95% confidence interval, -1.11 to -0.65) to 0.035 (95% confidence interval, 0.016-0.054). Further analysis showed no significant improvement in the fit of survival models if storage time adjusted scores were included in the models rather than unadjusted scores. We then compared 3 ways of processing TMA sections after cutting-immediate staining, staining after 1 year, and staining after 1 year coated in wax-on the immunohistochemistry results for: progesterone receptor, a routinely used, robust antibody, and MKI67, which is generally considered less robust. The progesterone receptor scores for stored sections were similar to those for unstored sections, whereas the MKI67 scores for stored sections were substantially different to those for unstored sections. Wax coating made little difference to the results. Biomarker antigenicity shows a small decline over time that is unlikely to have an important effect on studies of prognostic biomarkers.
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