Laboratory of Innovation in Oncology, Clara Campal Comprehensive Cancer Centre (HM CIOCC), HM Sanchinarro University Hospital, Madrid, Spain.
Institute of Applied Molecular Medicine, Faculty of Medicine, Universidad San Pablo-CEU, Alcorcón, Madrid, Spain.
J Clin Invest. 2024 Apr 2;134(10):e176161. doi: 10.1172/JCI176161.
Cancer-derived small extracellular vesicles (sEVs) are capable of modifying the tumor microenvironment and promoting tumor progression. Ovarian cancer (OvCa) is a lethal malignancy that preferentially spreads through the abdominal cavity. Thus, the secretion of such vesicles into the peritoneal fluid could be a determinant factor in the dissemination and behavior of this disease. We designed a prospective observational study to assess the impact of peritoneal fluid-derived sEVs (PFD-sEVs) in OvCa clinical outcome. For this purpose, 2 patient cohorts were enrolled: patients with OvCa who underwent a diagnostic or cytoreductive surgery and nononcological patients, who underwent abdominal surgery for benign gynecological conditions and acted as the control group. Systematic extraction of PFD-sEVs from surgical samples enabled us to observe significant quantitative and qualitative differences associated with cancer diagnosis, disease stage, and platinum chemosensitivity. Proteomic profiling of PFD-sEVs led to the identification of molecular pathways and proteins of interest and to the biological validation of S100A4 and STX5. In addition, unsupervised analysis of PFD-sEV proteomic profiles in high-grade serous ovarian carcinomas (HGSOCs) revealed 2 clusters with different outcomes in terms of overall survival. In conclusion, comprehensive characterization of PFD-sEV content provided a prognostic value with potential implications in HGSOC clinical management.
肿瘤来源的小细胞外囊泡 (sEVs) 能够改变肿瘤微环境并促进肿瘤进展。卵巢癌 (OvCa) 是一种致命的恶性肿瘤,它优先通过腹腔扩散。因此,这些囊泡分泌到腹腔液中可能是这种疾病传播和行为的决定因素。我们设计了一项前瞻性观察研究,以评估腹腔液来源的 sEVs (PFD-sEVs) 在 OvCa 临床结局中的影响。为此,我们招募了 2 个患者队列:接受诊断性或细胞减灭性手术的 OvCa 患者和因良性妇科疾病接受腹部手术的非肿瘤患者作为对照组。从手术样本中系统地提取 PFD-sEVs,使我们能够观察到与癌症诊断、疾病阶段和铂类化疗敏感性相关的显著定量和定性差异。PFD-sEV 的蛋白质组学分析导致了对感兴趣的分子途径和蛋白质的鉴定,并对 S100A4 和 STX5 进行了生物学验证。此外,对高级别浆液性卵巢癌 (HGSOC) 的 PFD-sEV 蛋白质组分析的无监督分析揭示了 2 个具有不同总体生存结局的聚类。总之,对 PFD-sEV 内容的全面表征提供了具有潜在意义的预后价值,可能对 HGSOC 的临床管理产生影响。