The First Clinical Medical College, Xuzhou Medical University, 221000 Xuzhou, Jiangsu, China.
Department of Gynecology, The Affiliated Hospital of Xuzhou Medical University, 221000 Xuzhou, Jiangsu, China.
Front Biosci (Landmark Ed). 2023 Sep 24;28(9):220. doi: 10.31083/j.fbl2809220.
Activation of the signaling pathway is associated with tumorigenesis. The aim of this study was to investigate pathway gene functions and regulatory mechanisms in ovarian cancer (OC).
We conducted a bioinformatics analysis of publicly available datasets in order to identify potential -related mechanisms, associated genes, biological pathways, and their relation to immune function.
Significant differential expression of the pathway genes , , , , , , , , and was observed between OC samples and normal controls. Low expression of DLL4 and of in OC patients was associated with International Federation of Gynecology and Obstetrics (FIGO) stage (0.001 and = 0.036, respectively), while high expression of was associated with race ( = 0.039) and age ( = 0.044). JAG2 and expression were significantly associated with progression-free interval (PFI) ( = 0.011 and = 0.039, respectively). (Hazard Ratio (HR): 2.096; 95% CI: 1.522-2.886, 0.001) and (HR: 0.711; 95% CI: 0.514-0.983, = 0.039) expression were independently associated with PFI in multivariate analysis. , , , , and expression could significantly differentiate OC from non-cancer samples. Genes associated with the pathway were mainly enriched in five signaling pathways: the signaling pathway, breast cancer, endocrine resistance, Th1 and Th2 cell differentiation, and oxidative phosphorylation. The expression of pathway genes was significantly associated with immune cell infiltration.
pathway genes appear to play an important role in the progression of OC by regulating immune cells, endocrine resistance, Th1 and Th2 cell differentiation, and oxidative phosphorylation. and are potential biomarkers and therapeutic targets for the treatment of OC.
信号通路的激活与肿瘤发生有关。本研究旨在探讨卵巢癌(OC)中 通路基因的功能和调控机制。
我们对公共可用数据集进行了生物信息学分析,以确定潜在的相关机制、相关基因、生物途径及其与免疫功能的关系。
OC 样本与正常对照之间观察到 通路基因 、 、 、 、 、 、 和 的表达存在显著差异。OC 患者 DLL4 和 的低表达与国际妇产科联合会(FIGO)分期有关(分别为 0.001 和 = 0.036),而 的高表达与种族( = 0.039)和年龄( = 0.044)有关。JAG2 和 的表达与无进展生存期(PFI)显著相关( = 0.011 和 = 0.039)。多变量分析显示, (危险比(HR):2.096;95%置信区间(CI):1.522-2.886, 0.001)和 (HR:0.711;95% CI:0.514-0.983, = 0.039)的表达与 PFI 独立相关。 、 、 、 、 和 的表达可显著区分 OC 与非癌样本。与 通路相关的基因主要富集在五个信号通路中: 信号通路、乳腺癌、内分泌抵抗、Th1 和 Th2 细胞分化以及氧化磷酸化。 通路基因的表达与免疫细胞浸润显著相关。
通路基因通过调节免疫细胞、内分泌抵抗、Th1 和 Th2 细胞分化以及氧化磷酸化,在 OC 的进展中似乎发挥着重要作用。 和 可能是治疗 OC 的潜在生物标志物和治疗靶点。