Dual-Specificity Tyrosine Phosphorylation-Regulated Kinase 3 Expression and Its Correlation with Prognosis and Growth of Serous Ovarian Cancer: Correlation of DYRK3 with Ovarian Cancer Survival

Jia Sun, Yingzi Zhang, Aijie Li, Hao Yu
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Abstract

Background. Epithelial ovarian cancer, primarily serous ovarian cancer (SOC), stands as a predominant cause of cancer-related mortality among women globally, emphasizing the urgent need for comprehensive research into its molecular underpinnings. Within this context, the dual-specificity tyrosine phosphorylation-regulated kinase 3 (DYRK3) has emerged as a potential key player with implications for prognosis and tumor progression. Methods. This study conducted a meticulous retrospective analysis of 254 SOC cases from our medical center to unravel the prognostic significance of DYRK3. Survival analyses underscored DYRK3 as an independent adverse prognostic factor in SOC, with a hazard ratio of 2.60 (95% CI 1.67-4.07, P < 0.001). Experimental investigations involved DYRK3 knockdown in serous ovarian cancer cell lines (CAOV3 and OVCAR-3) through a shRNA strategy, revealing substantial decreases in cell growth and invasion capabilities. Bioinformatics analyses further hinted at DYRK3’s involvement in modulating the tumor immune microenvironment. In vivo experiments with DYRK3-knockdown cell lines validated these findings, demonstrating a notable restriction in the growth of ovarian cancer xenografts. Results. Our findings collectively illuminate DYRK3 as a pivotal tumor-promoting oncogene in SOC. Beyond its adverse prognostic implications, DYRK3 knockdown exhibited promising therapeutic potential by impeding cancer progression and potentially influencing the tumor immune microenvironment. Conclusions. This study establishes a compelling foundation for further research into DYRK3’s intricate role and therapeutic potential in ovarian cancer treatment. As we unravel the complexities surrounding DYRK3, our work not only contributes to the understanding of SOC pathogenesis but also unveils new prospects for targeted therapeutic interventions, holding promise for improved outcomes in ovarian cancer management.

Abstract Image

双特异性酪氨酸磷酸化调节激酶 3 的表达及其与浆液性卵巢癌的预后和生长的相关性:DYRK3与卵巢癌生存率的相关性
背景。上皮性卵巢癌,主要是浆液性卵巢癌(SOC),是全球妇女癌症相关死亡的主要原因,因此迫切需要对其分子基础进行全面研究。在此背景下,双特异性酪氨酸磷酸化调控激酶 3(DYRK3)成为影响预后和肿瘤进展的潜在关键因素。研究方法本研究对本医疗中心的 254 例 SOC 病例进行了细致的回顾性分析,以揭示 DYRK3 的预后意义。生存分析显示,DYRK3 是 SOC 的独立不良预后因素,危险比为 2.60(95% CI 1.67-4.07,)。实验研究通过 shRNA 策略在浆液性卵巢癌细胞系(CAOV3 和 OVCAR-3)中敲除 DYRK3,结果显示细胞生长和侵袭能力大幅下降。生物信息学分析进一步表明,DYRK3 参与了肿瘤免疫微环境的调节。使用 DYRK3 敲除细胞系进行的体内实验验证了这些发现,表明卵巢癌异种移植物的生长明显受到限制。结果。我们的研究结果共同揭示了 DYRK3 是 SOC 中一个关键的肿瘤促进癌基因。除了对预后的不利影响外,DYRK3 基因敲除还通过阻碍癌症进展和潜在地影响肿瘤免疫微环境展现出了良好的治疗潜力。结论这项研究为进一步研究 DYRK3 在卵巢癌治疗中的复杂作用和治疗潜力奠定了令人信服的基础。随着我们揭开围绕 DYRK3 的复杂性,我们的工作不仅有助于了解 SOC 的发病机制,还为靶向治疗干预开辟了新的前景,为改善卵巢癌的治疗效果带来了希望。
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Comparative and Functional Genomics
Comparative and Functional Genomics 生物-生化与分子生物学
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