PO.BCS01.14 · 生物信息与计算
知识图谱驱动的神经内分泌前列腺癌洞见与药物再利用机遇
Knowledge graph driven insights and drug repurposing opportunities for neuroendocrine prostate cancer
作者与单位 Authors & Affiliations
摘要 Abstract
中文摘要
生物医学知识图谱(BKG)已成为整合、管理和探索这一复杂信息领域的强大工具。Elucidata构建了一个整合20多个高质量、精心整理知识来源的知识图谱。此外,我们还开发了一款基于GUI的应用程序,使用户能够以无代码方式获得洞见。这有助于发现通过上游或下游网络效应调节靶点活性的药物。神经内分泌前列腺癌(NEPC)是前列腺癌的一种高度侵袭性组织学亚型。文献综述表明,NEPC药物再利用的“真正的生物学难题”并非疾病状态本身,而是治疗诱导的谱系可塑性这一潜在因果过程。该转变由RB1和TP53缺失所启动,并由相互增强的MYCN-AURKA-EZH2调控轴所维持。这一转变的结果是常规治疗靶点(如AR和PSMA)的丧失,以及新的可干预脆弱性的出现——包括AURKA、EZH2、BCL2和DLL3。其不良临床结局源于检测延迟、疾病快速进展以及缺乏有效治疗选择的共同作用。此外,公开可用的NEPC数据集数量极少,阻碍了早期研发。我们展示了如何查询知识图谱以鉴定具有与MYCN必需性相似依赖谱的基因。具有相似必需性谱的基因几乎总是功能相关(例如属于同一复合物或通路)。我们进一步提供了已获批用于其他疾病、且与NEPC具有共同分子基础的药物的证据,这些药物可能被推进临床试验以治疗NEPC。
查看英文原文 English abstract
Biomedical Knowledge Graphs (BKGs) have emerged as powerful tools for integrating, managing, and exploring this complex information landscape. Elucidata has built a knowledge graph that integrates 20+ high-quality, well-curated knowledge sources. Additionally, we have developed a GUI-based application that enables users to derive insights in a no-code manner. This facilitates the discovery of drugs that modulate a target's activity through upstream or downstream network effects.Neuroendocrine prostate cancer (NEPC) represents a highly aggressive histologic subtype of prostate cancer. Literature review shows that the “true biological problem” for drug repurposing in NEPC is not the disease state itself, but the underlying causal process of treatment-induced lineage plasticity. This transition is initiated by RB1 and TP53 loss and sustained by a mutually reinforcing MYCN-AURKA-EZH2 regulatory axis. The outcome of this shift is the loss of conventional therapeutic targets (such as AR and PSMA) and the emergence of new, actionable vulnerabilities-including AURKA, EZH2, BCL2, and DLL3.Its poor clinical outcomes stem from a combination of delayed detection, rapid disease progression, and the absence of effective therapeutic options. Additionally, the number of publicly available NEPC datasets is very low, hampering early-stage R&D. We demonstrate how knowledge graphs can be queried to identify genes with dependency profiles similar to MYCN's essentiality. Genes with similar essentiality profiles are almost always functionally related (e.g., belonging to the same complex or pathway). We further provide evidence for drugs approved for other diseases that share molecular underpinnings with NEPC and may be advanced into clinical trials to treat NEPC.
利益披露 Disclosure
P. Verma, None..
P. Sekar, None..
D. Dadi, None..
M. Sen, None..
N. Dhruw, None..
A. Jha, None.