Expression of estrogen receptor beta isoforms in pancreatic adenocarcinoma
Document Type
Journal Article
Publication Date
12-1-2018
Journal
Oncotarget
Volume
9
Issue
102
DOI
10.18632/oncotarget.26503
Keywords
Estrogen receptor; Image analysis; Pancreas; Proliferative activity; Quantitative biomarker analysis
Abstract
Copyright: Younes et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Limited studies have shown that some patients with pancreatic adenocarcinoma (PAC) may benefit from treatment with tamoxifen. PAC has been shown to be largely negative for estrogen receptor alpha (ER-alpha). The aim of this pilot study was to investigate ER-beta expression in human PAC. Sections of tissue microarray with 18 evaluable cases of human PAC were stained by immunohistochemistry (IHC) for ER-beta1, ER-beta2, ER-beta5, and Cyclin A. The levels of ER-beta isoform expression and the S-phase fraction (SPF) were determined using quantitative digital image analysis. Higher mean and median ER-beta2 levels correlated with male sex (p = 0.057 and p = 0.035, respectively), older age (p = 0.005 and p = 0.006, respectively), and lower pT stage (p = 0.008 and p = 0.009). Mean and median ER-beta5 levels correlated negatively with SPF (p = 0.021 and p = 0.047, respectively). Mean ER-beta1 expression did not correlate with any of the above mentioned clinicopathologic factors. The findings in this pilot study, although should be considered preliminary, suggest that some ER-beta isoforms may play a role in the biology of PAC. Additional larger studies are needed to confirm our findings, and to determine whether ER-beta may be considered for future targeted therapy.
APA Citation
Younes, M., Ly, C., Singh, K., Ertan, A., Younes, P., & Bailey, J. (2018). Expression of estrogen receptor beta isoforms in pancreatic adenocarcinoma. Oncotarget, 9 (102). http://dx.doi.org/10.18632/oncotarget.26503