Shafi Ayesha A, Schiewer Matthew J, de Leeuw Renée, Dylgjeri Emanuela, McCue Peter A, Shah Neelima, Gomella Leonard G, Lallas Costas D, Trabulsi Edouard J, Centenera Margaret M, Hickey Theresa E, Butler Lisa M, Raj Ganesh, Tilley Wayne D, Cukierman Edna, Knudsen Karen E
Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA, USA.
Cancer Biology, Fox Chase Cancer Center, Temple Health, Philadelphia, PA, USA.
Eur Urol Oncol. 2018 Sep;1(4):325-337. doi: 10.1016/j.euo.2018.04.019. Epub 2018 Jun 6.
Androgen deprivation therapy is a first-line treatment for disseminated prostate cancer (PCa). However, virtually all tumors become resistant and recur as castration-resistant PCa, which has no durable cure. One major hurdle in the development of more effective therapies is the lack of preclinical models that adequately recapitulate the heterogeneity of PCa, significantly hindering the ability to accurately predict therapeutic response.
To leverage the ex vivo culture method termed (PDE) to examine the impact of PCa therapeutics on a patient-by-patient basis.
Fresh PCa tissue from patients who underwent radical prostatectomy was cultured as PDEs to examine therapeutic response.
The impact of genomic and chemical perturbations in PDEs was assessed using various parameters (eg, AR levels, Ki67 staining, and desmoplastic indices).
PDE maintained the integrity of the native tumor microenvironment (TME), tumor tissue morphology, viability, and endogenous hormone signaling. Tumor cells in this model system exhibited de novo proliferative capacity. Examination of the native TME in the PDE revealed a first-in-field insight into patient-specific desmoplastic stromal indices and predicted responsiveness to AR-directed therapeutics.
The PDE model allows for a comprehensive evaluation of individual tumors in their native TME to ultimately develop more effective therapeutic regimens tailored to individuals. Discernment of novel stromal markers may provide a basis for applying precision medicine in treating advanced PCa, which would have a transformative effect on patient outcomes.
In this study, an innovative model system was used to more effectively mimic human disease. The patient-derived explant (PDE) system can be used to predict therapeutic response and identify novel targets in advanced disease. Thus, the PDE will be an asset for the development of novel metrics for the implementation of precision medicine in prostate cancer.The patient-derived explant (PDE) model allows for a comprehensive evaluation of individual human tumors in their native tumor microenvironment (TME). TME analysis revealed first-in-field insight into predicted tumor responsiveness to AR-directed therapeutics through evaluation of patient-specific desmoplastic stromal indices.
雄激素剥夺疗法是转移性前列腺癌(PCa)的一线治疗方法。然而,几乎所有肿瘤都会产生耐药性并复发为去势抵抗性前列腺癌,目前尚无持久的治愈方法。开发更有效疗法的一个主要障碍是缺乏能够充分概括前列腺癌异质性的临床前模型,这严重阻碍了准确预测治疗反应的能力。
利用称为患者来源外植体(PDE)的体外培养方法,逐例研究前列腺癌治疗方法的影响。
设计、设置和参与者:将接受根治性前列腺切除术患者的新鲜前列腺癌组织培养为PDEs,以研究治疗反应。
使用各种参数(如AR水平、Ki67染色和促结缔组织增生指数)评估PDEs中基因组和化学扰动的影响。
PDE维持了天然肿瘤微环境(TME)的完整性、肿瘤组织形态、活力和内源性激素信号传导。该模型系统中的肿瘤细胞表现出新生增殖能力。对PDE中天然TME的检查首次揭示了患者特异性促结缔组织增生基质指数,并预测了对AR导向疗法的反应性。
PDE模型允许在天然TME中对个体肿瘤进行全面评估,以最终制定更适合个体的有效治疗方案。识别新的基质标志物可能为在晚期PCa治疗中应用精准医学提供基础,这将对患者预后产生变革性影响。
在本研究中,使用了一种创新的模型系统来更有效地模拟人类疾病。患者来源外植体(PDE)系统可用于预测治疗反应并识别晚期疾病中的新靶点。因此,PDE将成为开发用于在前列腺癌中实施精准医学的新指标的一项资产。患者来源外植体(PDE)模型允许在其天然肿瘤微环境(TME)中对个体人类肿瘤进行全面评估。TME分析通过评估患者特异性促结缔组织增生基质指数,首次揭示了对预测的肿瘤对AR导向疗法反应性的见解。