Department of Gynecology, Division of Gynecology and Obstetrics, University Medical Centre Ljubljana, Zaloška 2, SI-1000 Ljubljana, Slovenia.
Department of Gynecology and Obstetrics, Faculty of Medicine, University of Ljubljana, Šlajmerjeva 3, SI-1000 Ljubljana, Slovenia.
Int J Mol Sci. 2024 Sep 23;25(18):10195. doi: 10.3390/ijms251810195.
Ovarian cancer (OC), particularly high-grade serous carcinoma (HGSC), is a leading cause of gynecological cancer mortality due to late diagnosis and chemoresistance. While studies on OC cell lines have shown that overexpression of the ATP7A membrane transporter correlates with resistance to platinum-based drugs (PtBMs) and cross-resistance to copper (Cu), clinical evidence is lacking. The functionality of ceruloplasmin (CP), the main Cu-transporting protein in the blood, is dependent on, among other things, ATP7A activity. This study investigated ATP7A expression and CP levels as potential biomarkers for predicting responses to PtBMs. We included 28 HGSC patients who underwent neoadjuvant chemotherapy (NACT). ATP7A expression in ovarian and peritoneal tissues before NACT and in peritoneal and omental tissues after NACT was analyzed via qPCR, and CP levels in ascites and plasma were measured via ELISA before and after NACT. In total, 54% of patients exhibited ATP7A expression in pretreatment tissue (ovary and/or peritoneum), while 43% of patients exhibited ATP7A expression in tissue after treatment (peritoneum and/or omentum). A significant association was found between higher ATP7A expression in the peritoneum before NACT and an unfavorable CA-125 elimination rate constant k (KELIM) score. Patients with omental ATP7A expression had significantly higher plasma mean CP levels before NACT. Plasma CP levels decreased significantly after NACT, and higher CP levels after NACT were associated with a shorter platinum-free interval (PFI). These findings suggest that the ATP7A transporter and CP have the potential to serve as predictive markers of chemoresistance, but further research is needed to validate their clinical utility.
卵巢癌(OC),尤其是高级别浆液性癌(HGSC),由于诊断较晚和化疗耐药性,是妇科癌症死亡的主要原因。虽然 OC 细胞系的研究表明,ATP7A 膜转运体的过度表达与铂类药物(PtBMs)耐药性和铜(Cu)交叉耐药性相关,但临床证据不足。铜转运蛋白(CP)的主要功能,除其他外,还依赖于 ATP7A 活性。本研究调查了 ATP7A 表达和 CP 水平作为预测对 PtBMs 反应的潜在生物标志物。我们纳入了 28 名接受新辅助化疗(NACT)的 HGSC 患者。通过 qPCR 分析 NACT 前卵巢和腹膜组织以及 NACT 后腹膜和网膜组织中的 ATP7A 表达,并通过 ELISA 测量 NACT 前后腹水和血浆中的 CP 水平。总的来说,54%的患者在预处理组织(卵巢和/或腹膜)中表现出 ATP7A 表达,而 43%的患者在治疗后的组织(腹膜和/或网膜)中表现出 ATP7A 表达。NACT 前腹膜中 ATP7A 表达较高与 CA-125 消除率常数 k(KELIM)评分不良显著相关。NACT 前有网膜 ATP7A 表达的患者血浆平均 CP 水平显著升高。NACT 后血浆 CP 水平显著下降,NACT 后 CP 水平较高与无铂间隔时间(PFI)缩短相关。这些发现表明,ATP7A 转运体和 CP 有可能成为化疗耐药性的预测标志物,但需要进一步研究来验证其临床实用性。