Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, Canada.
Department of Molecular Oncology, BC Cancer, Vancouver, BC, Canada.
J Pathol. 2024 Oct;264(2):160-173. doi: 10.1002/path.6329. Epub 2024 Aug 3.
Clear cell ovarian carcinoma (CCOC) is an aggressive malignancy affecting younger women. Despite ovarian cancer subtypes having diverse molecular and clinical characteristics, the mainstay of treatment for advanced stage disease remains cytotoxic chemotherapy. Late stage CCOC is resistant to conventional chemotherapy, which means a suboptimal outcome for patients affected. Despite detailed genomic, epigenomic, transcriptomic, and proteomic characterisation, subtype-specific treatment for CCOC has shown little progress. The unique glycogen accumulation defining CCOC suggests altered metabolic pathway activity and dependency. This study presents the first metabolomic landscape of ovarian cancer subtypes, including 42 CCOC, 20 high-grade serous and 21 endometrioid ovarian carcinomas, together comprising the three most common ovarian carcinoma subtypes. We describe a distinct metabolomic landscape of CCOC compared with other ovarian cancer subtypes, including alterations in energy utilisation and cysteine metabolism. In addition, we identify CCOC-specific alterations in metabolic pathways including serine biosynthesis and ROS-associated pathways that could serve as potential therapeutic targets. Our study provides the first in-depth study into the metabolome of ovarian cancers and a rich resource to support ongoing research efforts to identify subtype-specific therapeutic targets that could improve the dismal outcome for patients with this devastating malignancy. © 2024 The Author(s). The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.
透明细胞卵巢癌(CCOC)是一种侵袭性恶性肿瘤,影响年轻女性。尽管卵巢癌亚型具有不同的分子和临床特征,但晚期疾病的主要治疗方法仍然是细胞毒性化疗。晚期 CCOC 对常规化疗具有抗性,这意味着受影响患者的预后不佳。尽管进行了详细的基因组、表观基因组、转录组和蛋白质组学特征分析,但针对 CCOC 的亚型特异性治疗进展甚微。定义 CCOC 的独特糖原积累表明代谢途径活性和依赖性发生改变。本研究首次展示了卵巢癌亚型的代谢组学图谱,包括 42 例 CCOC、20 例高级别浆液性和 21 例子宫内膜样卵巢癌,这三种是最常见的卵巢癌亚型。与其他卵巢癌亚型相比,我们描述了 CCOC 独特的代谢组学图谱,包括能量利用和半胱氨酸代谢的改变。此外,我们还确定了 CCOC 特异性代谢途径的改变,包括丝氨酸生物合成和与 ROS 相关的途径,这些可能成为潜在的治疗靶点。本研究首次深入研究了卵巢癌的代谢组学,并为正在进行的研究提供了丰富的资源,以确定亚型特异性的治疗靶点,从而改善这种毁灭性恶性肿瘤患者的不良预后。