Wu You, Wang Kunyu, Song Yan, Li Bin
Department of Gynecology Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Department of Pathology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Transl Oncol. 2025 Sep;59:102439. doi: 10.1016/j.tranon.2025.102439. Epub 2025 Jun 27.
Gynecological malignancies, particularly ovarian cancer, pose a formidable challenge to women's wellbeing, as evidenced by the global incidence and mortality rates, emphasizing the pressing need for advanced diagnostic and treatment modalities. The heterogeneity of ovarian cancer poses challenges for traditional therapeutic approaches, necessitating the exploration of novel, precision medicine techniques.
This study leveraged multi-dataset analysis to construct and validate an Artificial Intelligence-Derived Prognostic Index (AIDPI) for ovarian cancer. Transcriptome data from the TCGA, ICGC, and GEO databases were utilized, encompassing bulk and single-cell RNA sequencing. The AIDPI model was developed and refined using univariate Cox regression analysis and an ensemble of machine learning algorithms. Functional analysis, immunoprofiling, and the role of the MFAP4 gene were investigated to elucidate the biological mechanisms underlying the model.
The AIDPI model demonstrated superior accuracy in predicting ovarian cancer prognosis compared to existing models. It correlated with clinical treatment outcomes, including chemotherapy responsiveness, and was integrated into a nomogram for improved prognostic stratification. Functional analysis revealed the influence of AIDPI genes on tumor immune infiltration and cell cycle regulation. Single-cell analysis exposed cell type-specific expression patterns, and the MFAP4 gene was identified as a potential therapeutic target due to its association with patient prognosis and modulation of cellular behavior. In clinical samples of ovarian cancer patients, MFAP4 is highly expressed in metastatic lesions and is associated with poor prognosis. In vitro and in vivo experiments, knockdown of MFAP4 reduces the metastasis of ovarian cancer cells.
The AIDPI model offers a highly accurate tool for ovarian cancer prognosis and treatment decision-making, underscored by the integration of multi-omics data and artificial intelligence. The model's performance and biological insights provide a foundation for advancing precision medicine in ovarian cancer. MFAP4's functionality and the influence of DNA methylation present opportunities for prospective research endeavors and potential therapeutic interventions.
妇科恶性肿瘤,尤其是卵巢癌,对女性健康构成了巨大挑战,全球发病率和死亡率就是明证,这凸显了对先进诊断和治疗方式的迫切需求。卵巢癌的异质性给传统治疗方法带来了挑战,因此需要探索新的精准医学技术。
本研究利用多数据集分析构建并验证了一种用于卵巢癌的人工智能衍生预后指数(AIDPI)。使用了来自TCGA、ICGC和GEO数据库的转录组数据,包括批量和单细胞RNA测序。通过单变量Cox回归分析和一系列机器学习算法开发并完善了AIDPI模型。研究了功能分析、免疫图谱以及MFAP4基因的作用,以阐明该模型背后的生物学机制。
与现有模型相比,AIDPI模型在预测卵巢癌预后方面表现出更高的准确性。它与临床治疗结果相关,包括化疗反应性,并被整合到一个列线图中以改善预后分层。功能分析揭示了AIDPI基因对肿瘤免疫浸润和细胞周期调控的影响。单细胞分析揭示了细胞类型特异性表达模式,由于MFAP4基因与患者预后及细胞行为调节相关,因此被确定为一个潜在的治疗靶点。在卵巢癌患者的临床样本中,MFAP4在转移病灶中高表达,且与预后不良相关。在体外和体内实验中,敲低MFAP4可减少卵巢癌细胞的转移。
AIDPI模型为卵巢癌预后和治疗决策提供了一个高度准确的工具,多组学数据与人工智能的整合突出了这一点。该模型的性能和生物学见解为推进卵巢癌精准医学奠定了基础。MFAP4的功能以及DNA甲基化的影响为前瞻性研究努力和潜在治疗干预提供了机会。