Wang Xiaoying, Duan Maoteng, Su Po-Lan, Li Jianying, Krull Jordan, Jin Jiacheng, Chen Hu, Sun Yuhan, Wu Weidong, He Kai, Carpenter Richard L, Zhang Chi, Cao Sha, Xu Dong, Wang Guangyu, Li Lang, Xin Gang, Carbone David P, Li Zihai, Ma Qin
Department of Biomedical Informatics, College of Medicine, The Ohio State University, Columbus, OH, 43210, USA.
Pelotonia Institute for Immuno-Oncology, The James Comprehensive Cancer Center, The Ohio State University, Columbus, OH 43210, USA.
bioRxiv. 2025 May 22:2025.05.16.654579. doi: 10.1101/2025.05.16.654579.
Metastasis remains the leading cause of cancer-related mortality, yet predicting future metastasis is a major clinical challenge due to the lack of validated biomarkers and effective assessment methods. Here, we present EmitGCL, a deep-learning framework that accurately predicts future metastasis and its corresponding biomarkers. Based on a comprehensive benchmarking comparison, EmitGCL outperformed other computational tools across six cancer types from seven cohorts of patients with superior sensitivity and specificity. It captured occult metastatic cells in a patient with a lymph node-negative breast cancer, who was declared to have no evidence of disease by conventional imaging methods but was later confirmed to have a metastatic disease. Notably, EmitGCL identified and as predictable biomarkers for future breast cancer metastasis, which was validated across five independent cohorts of patients (n=420). Furthermore, we demonstrated YY1 transcription factor as a key driver of breast cancer metastasis which was validated through and CRISPR-based migration assays, suggesting that YY1 is a potential therapeutic target for deterring metastasis.
转移仍然是癌症相关死亡的主要原因,然而,由于缺乏经过验证的生物标志物和有效的评估方法,预测未来转移是一项重大的临床挑战。在此,我们展示了EmitGCL,这是一个深度学习框架,能够准确预测未来转移及其相应的生物标志物。基于全面的基准比较,EmitGCL在来自七个患者队列的六种癌症类型中表现优于其他计算工具,具有更高的敏感性和特异性。它在一名淋巴结阴性乳腺癌患者中捕获了隐匿性转移细胞,该患者通过传统成像方法被宣布没有疾病证据,但后来被证实患有转移性疾病。值得注意的是,EmitGCL确定 和 作为未来乳腺癌转移的可预测生物标志物,这在五个独立的患者队列(n = 420)中得到了验证。此外,我们证明YY1转录因子是乳腺癌转移的关键驱动因素,这通过 和基于CRISPR的迁移试验得到了验证,表明YY1是阻止转移的潜在治疗靶点。