Department of Obstetrics and Gynecology, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, 90095, USA.
UCLA Eli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research, University of California Los Angeles, Los Angeles, CA, 90095, USA.
Reprod Sci. 2020 Sep;27(9):1778-1790. doi: 10.1007/s43032-020-00175-w. Epub 2020 Mar 2.
Progesterone therapy is a viable treatment for complex atypical hyperplasia (CAH) and endometrial adenocarcinoma, though reliable molecular determinants of response are not available. To explore if analysis of pre-therapy endometrial biopsies could yield biomarkers of response to progesterone, patients with CAH or adenocarcinoma undergoing treatment with progestins were included in this cross-sectional study. Immunohistochemistry for progesterone receptor (PR) was performed. Manual PR expression scores (PRES) were first calculated for biopsies by counting PR-positive nuclei in 12 sensitive vs 9 resistant samples. Significant differences in manual PRES were detected in the stroma (p < 0.01) and total endometrium (p < 0.01) for sensitive vs resistant patients. Manual PRES in the stroma had the highest accuracy in segregating sensitive vs resistant patients (96%). Differences in epithelial PRES were not significant. To validate these findings, a correlation between manual PRES and visual PRES was performed in the 21 patients. An additional 11 patients were analyzed to test if visual PRES would be predictive of response to progesterone. Visual PRES in epithelia and stroma in the 32 specimens was calculated. Significant differences in visual PRES were detected in the stroma for sensitive vs resistant samples (p < 0.01), while differences in epithelial and total endometrium were not significant. Whole genome bisulfite sequencing was performed on DNA isolated using pre-therapy biopsies from 6 sensitive and 6 resistant patients in this cohort. Differentially methylated regions were identified in the stroma and epithelium when evaluating sensitive vs resistant samples. Pathways involved in cell adhesion demonstrated the greatest difference in methylation in these samples.
孕激素治疗是复杂非典型增生 (CAH) 和子宫内膜腺癌的可行治疗方法,尽管目前还没有可靠的反应分子决定因素。为了探讨在孕激素治疗前的子宫内膜活检中是否可以获得孕激素反应的生物标志物,本研究纳入了接受孕激素治疗的 CAH 或腺癌患者。对孕激素受体 (PR) 进行免疫组织化学染色。首先通过计算 12 个敏感样本和 9 个耐药样本中 PR 阳性核来计算活检的手动 PR 表达评分 (PRES)。在敏感和耐药患者的间质 (p < 0.01) 和整个子宫内膜 (p < 0.01) 中,手动 PRES 存在显著差异。间质中手动 PRES 对区分敏感和耐药患者的准确性最高 (96%)。上皮 PRES 的差异不显著。为了验证这些发现,在 21 名患者中对手动 PRES 和视觉 PRES 进行了相关性分析。另外分析了 11 名患者,以测试视觉 PRES 是否可以预测孕激素的反应。在 32 个标本中计算了上皮和间质的视觉 PRES。在敏感和耐药样本中,间质中的视觉 PRES 存在显著差异 (p < 0.01),而上皮和整个子宫内膜的差异不显著。对本队列中 6 名敏感和 6 名耐药患者的孕激素治疗前活检进行全基因组亚硫酸氢盐测序。在评估敏感和耐药样本时,在间质和上皮中鉴定出差异甲基化区域。在这些样本中,细胞黏附途径的甲基化差异最大。