Immunohistochemiluminescence detection: a quantitative tool in breast cancer HER-2 status evaluation

Her-2 status evaluation in breast cancer has prognostic and treatment response value but its interobserver variation among pathologists is a problem since it is not quantitatively assayed. This study presents an immunohistochemiluminescence method to quantify Her-2 in breast cancer. Anti-Her-2 antib...

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Published inDisease markers Vol. 34; no. 5; pp. 373 - 377
Main Authors de Melo Rêgo, Moacyr Jesus Barreto, Cordeiro, Marina Ferraz, Cavalcanti, Carmelita de Lima Bezerra, de Carvalho Junior, Luiz Bezerra, Beltrão, Eduardo Isidoro Carneiro
Format Journal Article
LanguageEnglish
Published IOS Press 01.01.2013
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Summary:Her-2 status evaluation in breast cancer has prognostic and treatment response value but its interobserver variation among pathologists is a problem since it is not quantitatively assayed. This study presents an immunohistochemiluminescence method to quantify Her-2 in breast cancer. Anti-Her-2 antibody was conjugated to acridinium ester (AE) and used to evaluate/quantify Her-2 status in breast Invasive Ductal Carcinoma (IDC, n = 50) comparing with traditional immunohistochemistry. Anti-HER-2-AE results were expressed in Relative Lights Units (RLU) and showed to be able to distinguish and quantify the differences between the three groups of Her-2 status. 3+ Her-2 status presented the highest RLU (246,982 × 10 3 ± 2.061 × 10 3 ) compared to 2+ (76,146 × 10 3 ± 0.290 × 10 3 ), negative (27,415 × 10 3 ± 1.445 × 10 3 ) and normal tissues (27,064 × 10 3 ± 2.060). Status differences were significant between 3+ and 2+ ( p = 0.0025); 2+ and negative ( p = 0.0003), and +3 and +1 ( p = 0.0001) beside this, normal breast control RLU was 27,064 × 10 3 ± 2,060 × 10 3 , similar to negative cases. Results showed that anti-HER-2-AE conjugate was effective in breast tumors Her-2 status evaluation, allowing its quantitative establishment to consequently decrease the subjectivity in prognostic and predictive information intrinsic to this test.
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ISSN:0278-0240
1875-8630
DOI:10.3233/DMA-130981