The First Department of Oncologic Gynecology and Gynecology, Medical University of Lublin, 20-081 Lublin, Poland.
Department of Biochemistry and Molecular Biology, Medical University of Lublin, 20-081 Lublin, Poland.
Cells. 2023 Feb 23;12(5):701. doi: 10.3390/cells12050701.
: Ovarian cancer (OC) is the most lethal malignancy of the female reproductive tract. Consequently, a better understanding of the malignant features in OC is pertinent. Mortalin (mtHsp70/GRP75/PBP74/HSPA9/HSPA9B) promotes cancer development, progression, metastasis, and recurrence. Yet, there is no parallel evaluation and clinical relevance of mortalin in the peripheral and local tumor ecosystem in OC patients. : A cohort of 92 pretreatment women was recruited, including 50 OC patients, 14 patients with benign ovarian tumors, and 28 healthy women. Blood plasma and ascites fluid-soluble mortalin concentrations were measured by ELISA. Mortalin protein levels in tissues and OC cells were analyzed using proteomic datasets. The gene expression profile of mortalin in ovarian tissues was evaluated through the analysis of RNAseq data. Kaplan-Meier analysis was used to demonstrate the prognostic relevance of mortalin. : First, we found upregulation of local mortalin in two different ecosystems, i.e., ascites and tumor tissues in human OC compared to control groups. Second, abundance expression of local tumor mortalin is associated with cancer-driven signaling pathways and worse clinical outcome. Third, high mortalin level in tumor tissues, but not in the blood plasma or ascites fluid, predicts worse patient prognosis. : Our findings demonstrate a previously unknown mortalin profile in peripheral and local tumor ecosystem and its clinical relevance in OC. These novel findings may serve clinicians and investigators in the development of biomarker-based targeted therapeutics and immunotherapies.
卵巢癌(OC)是女性生殖道最致命的恶性肿瘤。因此,更好地了解 OC 的恶性特征是相关的。Mortalin(mtHsp70/GRP75/PBP74/HSPA9/HSPA9B)促进癌症的发展、进展、转移和复发。然而,在 OC 患者的外周和局部肿瘤生态系统中,并没有对 mortalin 进行平行评估和临床相关性研究。
我们招募了 92 名预处理女性,包括 50 名 OC 患者、14 名良性卵巢肿瘤患者和 28 名健康女性。通过 ELISA 测量血浆和腹水可溶性 mortalin 浓度。使用蛋白质组数据集分析组织和 OC 细胞中的 mortalin 蛋白水平。通过分析 RNAseq 数据评估卵巢组织中 mortalin 的基因表达谱。Kaplan-Meier 分析用于证明 mortalin 的预后相关性。
首先,我们发现与对照组相比,人 OC 中的两种不同生态系统,即腹水和肿瘤组织中的局部 mortalin 上调。其次,局部肿瘤 mortalin 的丰度表达与癌症驱动的信号通路相关,且临床结局较差。第三,肿瘤组织中高 mortalin 水平,而不是血浆或腹水中的水平,预测患者预后较差。
我们的研究结果表明,在 OC 中,外周和局部肿瘤生态系统中存在以前未知的 mortalin 谱及其临床相关性。这些新发现可能为临床医生和研究人员开发基于生物标志物的靶向治疗和免疫疗法提供参考。