2022-RA-1251-ESGO P-cadherin: a promising prognostic biomarker for homologous repair proficient high grade serous ovarian carcinoma

R. Canario, Inês Morgado, A. Ribeiro, N. Mendes, P. Lopes, M. Teixeira, C. Bartosch, J. Paredes
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Abstract

acquired platinum resistance in many cases, and emerging evidence suggests epigenetic alterations may be critical. We wish to investigate epigenetic changes that may drive platinum resistance in HGSC by treating established HGSC cell lines and patient-derived cells with pulses of carboplatin and investigating the nature, kinetics and plasticity of platinuminduced epigenetic changes. Methodology We will mimic, using in an in vitro two-dimensional model, multiple cycles of platinum-based chemotherapy as used clinically. We will generate preliminary results from established cell lines and primary cultures. The primary cell cultures are collected from the ascites of patients with HGSC treated at Imperial College NHS Trust, London. Following validation (p53, PAX8 immunocytochemistry), carboplatin sensitivity is assessed (sulforhodamine B assay). Cells are then pulsed with four cycles of carboplatin (50mM for 6 hours) with a week of recovery between each cycle. Chemosensitivity of surviving cells is measured after each cycle. The cells are then harvested for downstream methylation (Illumina 850k array), transcriptomic (RNA sequencing) and chromatin accessibility (ATAC sequencing) assays. Cells are also imaged using STORM (Stochastic Optical Reconstruction Microscopy). Preliminary STORM data already indicate differences in chromatin structure and the distribution of specific histone modifications between paired sensitive and resistant HGSC cell lines. Results We will receive the raw data within 8–12 weeks from now for the bioinformatic analysis. Differential gene expression analysis will uncover differently enriched pathways under the selective pressure of platinum-based chemotherapy. Conclusion Understanding the epigenetic landscape of HGSC in real time using physiologically relevant models will allow us to identify possible therapeutic targets that could eventually prevent platinum resistance.
2022-RA-1251-ESGO p -钙粘蛋白:一种有希望的同源修复高级别浆液性卵巢癌的预后生物标志物
在许多病例中获得性铂耐药,新出现的证据表明表观遗传改变可能至关重要。我们希望通过用卡铂脉冲处理已建立的HGSC细胞系和患者来源的细胞,并研究铂诱导的表观遗传变化的性质、动力学和可塑性,来研究可能驱动HGSC铂抗性的表观遗传变化。我们将在体外二维模型中模拟临床使用的多周期铂基化疗。我们将从已建立的细胞系和原代培养中产生初步结果。原代细胞培养物是从伦敦帝国学院NHS信托治疗的HGSC患者的腹水中收集的。验证后(p53, PAX8免疫细胞化学),评估卡铂敏感性(硫代丹胺B测定)。然后用卡铂(50mM,持续6小时)脉冲四个周期的细胞,每个周期之间有一周的恢复时间。每个周期后检测存活细胞的化学敏感性。然后收集细胞进行下游甲基化(Illumina 850k阵列),转录组(RNA测序)和染色质可及性(ATAC测序)测定。细胞也使用STORM(随机光学重建显微镜)成像。STORM的初步数据已经表明,在配对的敏感和耐药HGSC细胞系之间,染色质结构和特定组蛋白修饰的分布存在差异。结果我们将在8-12周内收到原始数据,用于生物信息学分析。差异基因表达分析将揭示在铂基化疗的选择压力下不同富集的途径。结论利用生理学相关模型实时了解HGSC的表观遗传学景观将使我们能够确定可能的治疗靶点,从而最终预防铂耐药。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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