Walter Reed Army Medical Center, Washington DC, United States of America.
PLoS One. 2011;6(7):e21121. doi: 10.1371/journal.pone.0021121. Epub 2011 Jul 6.
Clear cell ovarian cancer is an epithelial ovarian cancer histotype that is less responsive to chemotherapy and carries poorer prognosis than serous and endometrioid histotypes. Despite this, patients with these tumors are treated in a similar fashion as all other ovarian cancers. Previous genomic analysis has suggested that clear cell cancers represent a unique tumor subtype. Here we generated the first whole genomic expression profiling using epithelial component of clear cell ovarian cancers and normal ovarian surface specimens isolated by laser capture microdissection. All the arrays were analyzed using BRB ArrayTools and PathwayStudio software to identify the signaling pathways. Identified pathways validated using serous, clear cell cancer cell lines and RNAi technology. In vivo validations carried out using an orthotopic mouse model and liposomal encapsulated siRNA. Patient-derived clear cell and serous ovarian tumors were grafted under the renal capsule of NOD-SCID mice to evaluate the therapeutic potential of the identified pathway. We identified major activated pathways in clear cells involving in hypoxic cell growth, angiogenesis, and glucose metabolism not seen in other histotypes. Knockdown of key genes in these pathways sensitized clear cell ovarian cancer cell lines to hypoxia/glucose deprivation. In vivo experiments using patient derived tumors demonstrate that clear cell tumors are exquisitely sensitive to antiangiogenesis therapy (i.e. sunitinib) compared with serous tumors. We generated a histotype specific, gene signature associated with clear cell ovarian cancer which identifies important activated pathways critical for their clinicopathologic characteristics. These results provide a rational basis for a radically different treatment for ovarian clear cell patients.
透明细胞卵巢癌是一种上皮性卵巢癌组织类型,对化疗的反应不如浆液性和子宫内膜样组织类型,预后也较差。尽管如此,这些肿瘤患者的治疗方式与所有其他卵巢癌患者相似。先前的基因组分析表明,透明细胞癌代表一种独特的肿瘤亚型。在这里,我们使用激光捕获显微切割分离的透明细胞卵巢癌上皮成分和正常卵巢表面标本进行了首次全基因组表达谱分析。使用 BRB ArrayTools 和 PathwayStudio 软件分析所有的阵列,以确定信号通路。使用浆液性、透明细胞癌细胞系和 RNAi 技术验证鉴定的途径。在体内使用原位小鼠模型和脂质体包裹的 siRNA 进行验证。将患者来源的透明细胞和浆液性卵巢肿瘤移植到 NOD-SCID 小鼠的肾包膜下,以评估鉴定途径的治疗潜力。我们确定了透明细胞中主要的激活途径,涉及缺氧细胞生长、血管生成和葡萄糖代谢,而这些途径在其他组织类型中没有发现。这些途径中的关键基因的敲低使透明细胞卵巢癌细胞系对缺氧/葡萄糖剥夺敏感。使用患者来源的肿瘤进行的体内实验表明,与浆液性肿瘤相比,透明细胞肿瘤对血管生成抑制治疗(即舒尼替尼)非常敏感。我们生成了一个与透明细胞卵巢癌相关的组织类型特异性基因特征,该特征确定了对其临床病理特征至关重要的重要激活途径。这些结果为卵巢透明细胞患者提供了一种截然不同的治疗方法提供了合理的依据。