PMID- 24427354 OWN - NLM STAT- MEDLINE DCOM- 20140905 LR - 20211021 IS - 1936-2625 (Electronic) IS - 1936-2625 (Linking) VI - 7 IP - 1 DP - 2014 TI - Evaluation of the progesterone receptor status in breast cancer using three different antibodies: a comparison by Allred score system. PG - 331-9 AB - Breast cancer (BC) hormonal receptors status is assessed by immunohistochemistry (IHC), a specific, sensitive, and accessible method that guide breast cancer treatment. In this study, we evaluated progesterone receptor (PR) expression in 53 BC cases using 3 anti-PgR antibodies (AB): monoclonal (SP42 and PgR636) and polyclonal ab62621. Primary BC cases (with signed informed consent) were used to generate tissue microarray platforms, where PR expression was accessed by IHC and evaluated by the Allred score. Categorical and quantitative data are shown in percentage and mean, respectively. Concordance (CON) and correlation among ABs were analyzed by Kappa factor (Kappa), Spearman's correlation coefficient (rho) or intraclass correlation coefficient. Staining patterns of each AB were compared by paired T-Test. We noted poor CON and Kappa between ab62621 vs SP42 (CON=64.1%; Kappa=0.247), and ab62621 vs PgR636 (CON=62.3%; Kappa=0.204), but higher CON between SP42 vs PgR636 (CON 90.6%; Kappa=0.738). Data were corroborated by Mc Nemar statistical test (p=0.019, p=0.014 and p>0.05, respectively). Regarding staining intensity (SI) among PgR+ samples, we found higher proportion of weak staining and lower SI for ab62621 (48.3%; mean IS=1.6), when compared to SP42 (20.0%, mean IS=2.1, T-test p<0.01) and PgR636 (2.3, 21.9%, T-test p<0.01). Within the entire sample, similar results were observed following rho: SP42 vs PgR636 (rho=0.8103); ab62621 vs SP42 (rho=0.3524); ab62621 vs PgR636 (rho=0.4075). As for proportion of stained cells and proportion score (PS), among PgR+ samples, the mean values for ab62621 (75.4%; 4.8) were significantly higher than those of SP42 (56.3%, 4.3; T-test p<0.01) and RPG636 (60.1%; 4.2; T-test p<0.01). Similar data were found after analyzing PS for the entire sample: SP42 vs PgR636 (rho=0.8588); SP42 vs ab62621 (rho=0.4832); RPG636 vs ab62621 (rho=0.4050). Our data indicate that anti-PgR monoclonal ABs, PgR636 and SP42, are, unlike ab62621, equally suitable to test BC PgR status by IHC due to their higher accuracy. Therefore, we suggest their clinical use during BC diagnosis; thus, enabling more precise therapeutic decisions to treat BC. FAU - Daltoe, Renata Dalmaschio AU - Daltoe RD AD - Biotechnology Program/RENORBIO, Federal University of Espirito Santo Brazil ; Department of Pharmacy and Nutrition, Federal University of Espirito Santo Brazil. FAU - Madeira, Klesia Pirola AU - Madeira KP AD - Biotechnology Program/RENORBIO, Federal University of Espirito Santo Brazil. FAU - de Carvalho, Alex Assis AU - de Carvalho AA AD - Department of Pathology, Federal University of Espirito Santo Brazil. FAU - de Rezende, Lucas Cunha Dias AU - de Rezende LC AD - Biotechnology Program/RENORBIO, Federal University of Espirito Santo Brazil. FAU - Silva, Ian Victor AU - Silva IV AD - Department of Morphology, Federal University of Espirito Santo Brazil. FAU - Rangel, Leticia Batista Azevedo AU - Rangel LB AD - Biotechnology Program/RENORBIO, Federal University of Espirito Santo Brazil ; Department of Pharmaceutical Sciences, Federal University of Espirito Santo Brazil. LA - eng PT - Comparative Study PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20131215 PL - United States TA - Int J Clin Exp Pathol JT - International journal of clinical and experimental pathology JID - 101480565 RN - 0 (Antibodies) RN - 0 (Antibodies, Monoclonal) RN - 0 (Receptors, Progesterone) SB - IM MH - Antibodies MH - *Antibodies, Monoclonal MH - Breast Neoplasms/*metabolism MH - Carcinoma/*metabolism MH - Female MH - Humans MH - Immunohistochemistry/*methods MH - Receptors, Progesterone/*analysis MH - Reproducibility of Results MH - Tissue Array Analysis PMC - PMC3885488 OTO - NOTNLM OT - Progesterone receptor OT - antibodies OT - breast cancer EDAT- 2014/01/16 06:00 MHDA- 2014/09/06 06:00 PMCR- 2013/12/15 CRDT- 2014/01/16 06:00 PHST- 2013/09/25 00:00 [received] PHST- 2013/10/15 00:00 [accepted] PHST- 2014/01/16 06:00 [entrez] PHST- 2014/01/16 06:00 [pubmed] PHST- 2014/09/06 06:00 [medline] PHST- 2013/12/15 00:00 [pmc-release] PST - epublish SO - Int J Clin Exp Pathol. 2013 Dec 15;7(1):331-9. eCollection 2014.