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Optimizing Ventana Chromogenic Dual In-situ Hybridization for Mucinous Epithelial Ovarian Cancer

Overview
Journal BMC Res Notes
Publisher Biomed Central
Date 2013 Dec 31
PMID 24373486
Citations 1
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Abstract

Background: Dual in-situ hybridization (DISH) assay is a relatively new assay for evaluating Human Epidermal Growth Factor Receptor 2 (HER2) genomic amplification. Optimization protocol for the assay is not yet well established, especially for archival tissues. Although there is a recommended nominal protocol, it is not suited for formalin-fixed and paraffin-embedded (FFPE) samples that were archived for long periods.

Findings: In a study on local population of mucinous epithelial ovarian cancer, we developed a series of optimization protocols based on the age of samples to improve success of the DISH assay. A decision workflow was generated to facilitate individualization of further optimization protocols. The optimizations were evaluated on 92 whole tissue sections of FFPE mucinous ovarian tumors dating from 1990 to 2011. Overall, 79 samples were successfully assayed for DISH using the series of optimization protocols. We found samples older than 1 year required further optimization beyond the nominal protocol recommended. Thirteen samples were not further assayed after first DISH assay due to inadequately preserved nuclear morphology with no ISH signals throughout the tissue section.

Conclusion: The study revealed age of samples and storage conditions were major factors in successful DISH assays. Samples that were ten years or less in age, and archived in-house were successfully optimized, whereas older samples, which were also archived off-site, have a higher frequency of unsuccessful optimizations. The study provides practical and important guidelines for the new DISH assay which can facilitate successful HER2 evaluation in ovarian cancers and possibly other cancers as well.

Citing Articles

Chromogenic In Situ Hybridization (CISH) as a Method for Detection of C-Myc Amplification in Formalin-Fixed Paraffin-Embedded Tumor Tissue: An Update.

Todorovic-Rakovic N Methods Mol Biol. 2021; 2318:313-320.

PMID: 34019299 DOI: 10.1007/978-1-0716-1476-1_17.

References
1.
Huang R, Chen G, Matsumura N, Lai H, Mori S, Li J . Histotype-specific copy-number alterations in ovarian cancer. BMC Med Genomics. 2012; 5:47. PMC: 3567940. DOI: 10.1186/1755-8794-5-47. View

2.
Mayr D, Kanitz V, Amann G, Engel J, Burges A, Lohrs U . HER-2/neu gene amplification in ovarian tumours: a comprehensive immunohistochemical and FISH analysis on tissue microarrays. Histopathology. 2006; 48(2):149-56. DOI: 10.1111/j.1365-2559.2005.02306.x. View

3.
Koh Y, Lee H, Lee J, Kang J, Gong G . Dual-color silver-enhanced in situ hybridization for assessing HER2 gene amplification in breast cancer. Mod Pathol. 2011; 24(6):794-800. DOI: 10.1038/modpathol.2011.9. View

4.
Anglesio M, Kommoss S, Tolcher M, Clarke B, Galletta L, Porter H . Molecular characterization of mucinous ovarian tumours supports a stratified treatment approach with HER2 targeting in 19% of carcinomas. J Pathol. 2012; 229(1):111-20. DOI: 10.1002/path.4088. View

5.
Gruver A, Peerwani Z, Tubbs R . Out of the darkness and into the light: bright field in situ hybridisation for delineation of ERBB2 (HER2) status in breast carcinoma. J Clin Pathol. 2010; 63(3):210-9. PMC: 2921277. DOI: 10.1136/jcp.2009.062760. View