CoTox：基于思维链的分子毒性推理与预测
CoTox: Chain-of-Thought-Based Molecular Toxicity Reasoning and Prediction
AI总结：
本文提出CoTox框架，将大语言模型与思维链推理结合，融合化学结构、生物通路和基因本体信息进行可解释的多毒性预测，并通过IUPAC命名和细胞生物学背景模拟提升性能，优于传统机器学习和深度学习模型。
摘要：
药物毒性仍然是药物开发中的主要挑战。最近的机器学习模型改善了计算机模拟毒性预测，但它们对标注数据的依赖以及缺乏可解释性限制了其适用性。这限制了它们捕捉由复杂生物机制驱动的器官特异性毒性的能力。大语言模型（LLMs）通过逐步推理和文本数据的整合提供了一种有前景的替代方案，然而先前的方法缺乏生物学背景和透明的推理依据。为了解决这一问题，我们提出了CoTox，一个将大语言模型与思维链（CoT）推理相结合用于多毒性预测的新型框架。CoTox结合化学结构数据、生物通路和基因本体（GO）术语，通过逐步推理生成可解释的毒性预测。使用GPT-4o，我们表明CoTox优于传统的机器学习模型和深度学习模型。我们进一步考察了它在各种大语言模型上的表现，以确定CoTox在哪些模型上最有效。此外，我们发现用IUPAC名称表示化学结构（相比SMILES，大语言模型更容易理解IUPAC名称）能够增强模型的推理能力并提高预测性能。为了展示其在药物开发中的实际效用，我们模拟了用药物处理相关细胞类型的过程，并将由此产生的生物学背景纳入CoTox框架。如案例研究所示，这种方法使CoTox能够生成与生理反应一致的毒性预测。这一结果凸显了基于大语言模型的框架在提高可解释性和支持早期药物安全性评估方面的潜力。本工作中使用的代码和提示可在https://github.com/dmis-lab/CoTox获取。
英文摘要：
Drug toxicity remains a major challenge in pharmaceutical development. Recent machine learning models have improved in silico toxicity prediction, but their reliance on annotated data and lack of interpretability limit their applicability. This limits their ability to capture organ-specific toxicities driven by complex biological mechanisms. Large language models (LLMs) offer a promising alternative through step-by-step reasoning and integration of textual data, yet prior approaches lack biological context and transparent rationale. To address this issue, we propose CoTox, a novel framework that integrates LLM with chain-of-thought (CoT) reasoning for multi-toxicity prediction. CoTox combines chemical structure data, biological pathways, and gene ontology (GO) terms to generate interpretable toxicity predictions through step-by-step reasoning. Using GPT-4o, we show that CoTox outperforms both traditional machine learning and deep learning model. We further examine its performance across various LLMs to identify where CoTox is most effective. Additionally, we find that representing chemical structures with IUPAC names, which are easier for LLMs to understand than SMILES, enhances the model's reasoning ability and improves predictive performance. To demonstrate its practical utility in drug development, we simulate the treatment of relevant cell types with drug and incorporated the resulting biological context into the CoTox framework. This approach allow CoTox to generate toxicity predictions aligned with physiological responses, as shown in case study. This result highlights the potential of LLM-based frameworks to improve interpretability and support early-stage drug safety assessment. The code and prompt used in this work are available at https://github.com/dmis-lab/CoTox.
机构、总结、中文摘要均由AI分析而来，可能存在错误，请以论文正文为准。
