Konstantinopoulos Panagiotis A, Matulonis Ursula A
Medical Gynecologic Oncology Program, Department of Medical Oncology, Dana Farber Cancer Institute, Harvard Medical School , Boston, MA , USA.
Front Oncol. 2013 Dec 11;3:296. doi: 10.3389/fonc.2013.00296.
Epithelial ovarian cancer (EOC) is the most lethal gynecologic malignancy and the fifth most common cause of female cancer death in the United States. Although important advances in surgical and chemotherapeutic strategies over the last three decades have significantly improved the median survival of EOC patients, the plateau of the survival curve has not changed appreciably. Given that EOC is a genetically and biologically heterogeneous disease, identification of specific molecular abnormalities that can be targeted in each individual ovarian cancer on the basis of predictive biomarkers promises to be an effective strategy to improve outcome in this disease. However, for this promise to materialize, appropriate preclinical experimental platforms that recapitulate the complexity of these neoplasms and reliably predict antitumor activity in the clinic are critically important. In this review, we will present the current status and evolution of preclinical models of EOC, including cell lines, immortalized normal cells, xenograft models, patient-derived xenografts, and animal models, and will discuss their potential for oncology drug development.
上皮性卵巢癌(EOC)是最致命的妇科恶性肿瘤,也是美国女性癌症死亡的第五大常见原因。尽管过去三十年手术和化疗策略取得了重要进展,显著提高了EOC患者的中位生存期,但生存曲线的平台期并未明显改变。鉴于EOC是一种基因和生物学上异质性的疾病,基于预测性生物标志物识别可在每个个体卵巢癌中靶向的特定分子异常,有望成为改善该疾病预后的有效策略。然而,要实现这一前景,重现这些肿瘤复杂性并可靠预测临床抗肿瘤活性的合适临床前实验平台至关重要。在本综述中,我们将介绍EOC临床前模型的现状和演变,包括细胞系、永生化正常细胞、异种移植模型、患者来源的异种移植模型和动物模型,并将讨论它们在肿瘤药物开发中的潜力。