Department of Molecular Carcinogenesis, Chiba Cancer Center Research Institute, Chiba 260-8717, Japan.
Cells. 2019 May 25;8(5):505. doi: 10.3390/cells8050505.
Ovarian cancer (OC) is one of the leading causes of female cancer death. Recent studies have documented its extensive variations as a disease entity, in terms of cell or tissue of origin, pre-cancerous lesions, common mutations, and therapeutic responses, leading to the notion that OC is a generic term referring to a whole range of different cancer subtypes. Despite such heterogeneity, OC treatment is stereotypic; aggressive surgery followed by conventional chemotherapy could result in chemo-resistant diseases. Whereas molecular-targeted therapies will become shortly available for a subset of OC, there still remain many patients without effective drugs, requiring development of groundbreaking therapeutic agents. In preclinical studies for drug discovery, cancer cell lines used to be the gold standard, but now this has declined due to frequent failure in predicting therapeutic responses in patients. In this regard, patient-derived cells and tumors are gaining more attention in precise and physiological modeling of in situ tumors, which could also pave the way to implementation of precision medicine. In this article, we comprehensively overviewed the current status of various platforms for patient-derived OC models. We highly appreciate the potentials of organoid culture in achieving high success rate and retaining tumor heterogeneity.
卵巢癌(OC)是女性癌症死亡的主要原因之一。最近的研究记录了其作为一种疾病实体的广泛变化,包括起源于细胞或组织、癌前病变、常见突变和治疗反应,这导致了 OC 是一个通用术语,指的是一系列不同的癌症亚型。尽管存在这种异质性,但 OC 的治疗方法是刻板的;积极的手术加常规化疗可能导致化疗耐药性疾病。虽然分子靶向治疗很快将可用于 OC 的一部分患者,但仍有许多患者没有有效的药物,需要开发开创性的治疗药物。在药物发现的临床前研究中,癌细胞系曾经是金标准,但由于经常无法预测患者的治疗反应,现在这种情况已经下降。在这方面,患者来源的细胞和肿瘤在原位肿瘤的精确和生理建模中受到越来越多的关注,这也为实施精准医学铺平了道路。在本文中,我们全面概述了各种患者来源的 OC 模型平台的现状。我们高度赞赏类器官培养在实现高成功率和保留肿瘤异质性方面的潜力。