Prostate-Specific Membrane Antigen Expression Is a Potential Prognostic Marker in Endometrial Adenocarcinoma

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Název: Prostate-Specific Membrane Antigen Expression Is a Potential Prognostic Marker in Endometrial Adenocarcinoma
Autoři: Mhawech-Fauceglia, P., Smiraglia, D. J., Bshara, W., Andrews, C., Schwaller, J., South, S., Higgs, D., Lele, S., Herrmann, F., Odunsi, K.
Zdroj: Cancer Epidemiology, Biomarkers & Prevention, Vol. 17, No 3 (2008) pp. 571-577
Informace o vydavateli: American Association for Cancer Research (AACR), 2008.
Rok vydání: 2008
Témata: Adult, Glutamate Carboxypeptidase II, 0301 basic medicine, Down-Regulation, Immunoenzyme Techniques, 618.97, 03 medical and health sciences, 0302 clinical medicine, Cell Line, Tumor, Biomarkers, Tumor, Humans, Aged, Proportional Hazards Models, Aged, 80 and over, Antigens, Surface/*metabolism, Analysis of Variance, Reverse Transcriptase Polymerase Chain Reaction, Middle Aged, Prognosis, Endometrial Neoplasms, 3. Good health, Glutamate Carboxypeptidase II/*metabolism, ddc:618.97, Antigens, Surface, Female, Endometrial Neoplasms/*metabolism, Tumor Markers, Biological/metabolism
Popis: The aim of this study was to determine the role of prostate-specific membrane antigen (PSMA) as a prognostic marker in endometrial adenocarcinoma (EAC) and to explore whether its down-regulation could be due to epigenetic mechanism. First, we examined the expression and the prognostic value of PSMA by semiquantitative reverse transcription-PCR and immunohistochemistry in EAC tissue samples. Second, to explore the role of CpG methylation in down-regulation PSMA in EAC, we evaluated PSMA CpG island methylation using methylation-specific PCR in cells lines and in a subset of patients' samples. Furthermore, association of the status of tumor methylation to the clinical and histologic variables was also evaluated. Higher PSMA mRNA levels were associated with stage I (P = 0.046) and PSMA protein intensity by immunohistochemistry (P = 0.032). In multivariate analysis, loss of PSMA expression was associated with a worse disease-free survival (P = 0.02). PSMA was methylated in prostate cell lines (DU145 and PC3) and endometrial cell lines. In addition, PSMA was methylated in 5 of 18 samples (all 5 had low PSMA mRNA value). There was a significant association between PSMA methylation and loss of protein expression by immunohistochemistry and PSMA-RNA level with P value of 0.036 and 0.011, respectively. In addition, there was an association between PSMA methylation and tumor size (P = 0.025). In summary, (a) PSMA is underexpressed in advanced stage EAC, (b) loss of PSMA expression can be considered as a prognostic marker in patients with EAC, and (c) loss of PSMA expression in a subset of EAC cases could be due to epigenetic silencing. (Cancer Epidemiol Biomarkers Prev 2008;17(3):571–7)
Druh dokumentu: Article
Popis souboru: application/pdf
Jazyk: English
ISSN: 1538-7755
1055-9965
DOI: 10.1158/1055-9965.epi-07-0511
Přístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/18349274
https://edoc.unibas.ch/29983/
https://www.ncbi.nlm.nih.gov/pubmed/18349274
https://cebp.aacrjournals.org/content/17/3/571.full.pdf+html
http://cebp.aacrjournals.org/content/17/3/571.full
https://cebp.aacrjournals.org/content/cebp/17/3/571.full.pdf
https://archive-ouverte.unige.ch/unige:19071
https://archive-ouverte.unige.ch/unige:19071
Přístupové číslo: edsair.doi.dedup.....b44ae2e9184c87891280031fd2b46d23
Databáze: OpenAIRE
Popis
Abstrakt:The aim of this study was to determine the role of prostate-specific membrane antigen (PSMA) as a prognostic marker in endometrial adenocarcinoma (EAC) and to explore whether its down-regulation could be due to epigenetic mechanism. First, we examined the expression and the prognostic value of PSMA by semiquantitative reverse transcription-PCR and immunohistochemistry in EAC tissue samples. Second, to explore the role of CpG methylation in down-regulation PSMA in EAC, we evaluated PSMA CpG island methylation using methylation-specific PCR in cells lines and in a subset of patients' samples. Furthermore, association of the status of tumor methylation to the clinical and histologic variables was also evaluated. Higher PSMA mRNA levels were associated with stage I (P = 0.046) and PSMA protein intensity by immunohistochemistry (P = 0.032). In multivariate analysis, loss of PSMA expression was associated with a worse disease-free survival (P = 0.02). PSMA was methylated in prostate cell lines (DU145 and PC3) and endometrial cell lines. In addition, PSMA was methylated in 5 of 18 samples (all 5 had low PSMA mRNA value). There was a significant association between PSMA methylation and loss of protein expression by immunohistochemistry and PSMA-RNA level with P value of 0.036 and 0.011, respectively. In addition, there was an association between PSMA methylation and tumor size (P = 0.025). In summary, (a) PSMA is underexpressed in advanced stage EAC, (b) loss of PSMA expression can be considered as a prognostic marker in patients with EAC, and (c) loss of PSMA expression in a subset of EAC cases could be due to epigenetic silencing. (Cancer Epidemiol Biomarkers Prev 2008;17(3):571–7)
ISSN:15387755
10559965
DOI:10.1158/1055-9965.epi-07-0511