PMID- 19675076 OWN - NLM STAT- MEDLINE DCOM- 20100216 LR - 20210816 IS - 1479-6821 (Electronic) IS - 1351-0088 (Linking) VI - 16 IP - 4 DP - 2009 Dec TI - Estrogen receptor 1 mRNA is a prognostic factor in ovarian carcinoma: determination by kinetic PCR in formalin-fixed paraffin-embedded tissue. PG - 1229-39 LID - 10.1677/ERC-08-0338 [doi] AB - Epidemiological and cell culture studies indicate that ovarian carcinoma growth is dependent on estrogen stimulation. However, possibly due to the lack of a reliable biomarker that helps to select patients according to prognostically relevant estrogen receptor (ER) levels, clinical trials using anti-estrogenic therapeutics in ovarian carcinoma have had inconsistent results. Therefore, we tested if ER expression analysis by a quantitative method might be useful in this regard in formalin-fixed paraffin-embedded (FFPE) tissue. In a study group of 114 primary ovarian carcinomas expression of estrogen receptor 1 (ESR1) mRNA was analyzed using a new method for RNA extraction from FFPE tissue that is based on magnetic beads, followed by kinetic PCR. The prognostic impact of ESR1 mRNA expression was investigated and compared to ERalpha protein expression as determined by immunohistochemistry. In univariate survival analysis the expression level of ESR1 mRNA was a significant positive prognostic factor for patient survival (hazard ratio (HR) 0.230 (confidence interval (CI) 0.102-0.516), P=0.002). ERalpha protein expression was correlated to ESR1 mRNA expression (P=0.0001); however, ERalpha protein expression did not provide statistically significant prognostic information. In multivariate analysis, ESR1 mRNA expression emerged as a prognostic factor, independent of stage, grade, residual tumor mass, age, and ERalpha protein expression (HR 0.227 (CI 0.078-0.656), P=0.006). Our results indicate that the determination of ESR1 levels by kinetic PCR may be superior to immunohistochemical methods in assessment of biologically relevant levels of ER expression in ovarian carcinoma, and is feasible in routinely used FFPE tissue. FAU - Darb-Esfahani, Silvia AU - Darb-Esfahani S AD - Institute of Pathology, Charite Universitatsmedizin Berlin, Berlin, Germany. silvia.darb-esfahani@charite.de FAU - Wirtz, Ralph M AU - Wirtz RM FAU - Sinn, Bruno V AU - Sinn BV FAU - Budczies, Jan AU - Budczies J FAU - Noske, Aurelia AU - Noske A FAU - Weichert, Wilko AU - Weichert W FAU - Faggad, Areeg AU - Faggad A FAU - Scharff, Susanne AU - Scharff S FAU - Sehouli, Jalid AU - Sehouli J FAU - Oskay-Ozcelik, Guelten AU - Oskay-Ozcelik G FAU - Zamagni, Claudio AU - Zamagni C FAU - De Iaco, Pierandrea AU - De Iaco P FAU - Martoni, Andrea AU - Martoni A FAU - Dietel, Manfred AU - Dietel M FAU - Denkert, Carsten AU - Denkert C LA - eng PT - Journal Article DEP - 20090812 PL - England TA - Endocr Relat Cancer JT - Endocrine-related cancer JID - 9436481 RN - 0 (Biomarkers, Tumor) RN - 0 (ESR1 protein, human) RN - 0 (Estrogen Receptor alpha) RN - 0 (RNA, Messenger) SB - IM MH - Adenocarcinoma, Clear Cell/genetics/metabolism/secondary MH - Adenocarcinoma, Mucinous/genetics/metabolism/secondary MH - Adult MH - Aged MH - Aged, 80 and over MH - Biomarkers, Tumor/genetics/metabolism MH - Carcinoma, Transitional Cell/genetics/metabolism/secondary MH - Cystadenocarcinoma, Serous/genetics/metabolism/secondary MH - Endometrial Neoplasms/genetics/metabolism/secondary MH - Estrogen Receptor alpha/*genetics/metabolism MH - Female MH - Humans MH - Immunoenzyme Techniques MH - Middle Aged MH - Ovarian Neoplasms/*genetics/metabolism/pathology MH - Paraffin Embedding MH - Prognosis MH - RNA, Messenger/*genetics/metabolism MH - Reverse Transcriptase Polymerase Chain Reaction EDAT- 2009/08/14 09:00 MHDA- 2010/02/17 06:00 CRDT- 2009/08/14 09:00 PHST- 2009/08/14 09:00 [entrez] PHST- 2009/08/14 09:00 [pubmed] PHST- 2010/02/17 06:00 [medline] AID - ERC-08-0338 [pii] AID - 10.1677/ERC-08-0338 [doi] PST - ppublish SO - Endocr Relat Cancer. 2009 Dec;16(4):1229-39. doi: 10.1677/ERC-08-0338. Epub 2009 Aug 12.