提出一种隐蔽的图神经网络后门攻击,可精准操控模型且不降低正常表现。
A Semantic and Clean-label Backdoor Attack against Graph Convolutional Networks
- 基于节点重要性选择语义触发器,无须改标签即可植入后门。
- 攻击成功率接近99%,污染样本占比低于3%。
- 适合关注图神经网络安全的研究者与防御开发者。
图卷积网络(GCNs)在节点分类和图分类等图结构任务中表现优异。然而,近期研究发现GCNs易受新型威胁——后门攻击的影响,攻击者可注入隐藏后门,使模型在良性样本上表现良好,一旦触发则预测结果被恶意篡改为指定目标标签。清洁标签后门攻击和语义后门攻击是针对深度神经网络的新威胁,更具隐蔽性且构成严重风险。目前,此类攻击在GCNs中的研究仍不充分。本文针对图分类任务,提出一种语义与清洁标签结合的后门攻击方法(SCLBA),以揭示GCNs存在的安全漏洞。SCLBA通过分析图样本中节点的重要性,选取特定类型节点作为语义触发器,将其插入图样本以生成污染样本,且不改变污染样本的真实标签。在多个数据集上的实验表明,该方法可在污染率低于3%的情况下实现接近99%的攻击成功率,同时对模型在良性样本上的性能几乎无影响。
原文摘要 · Abstract (English)
Graph Convolutional Networks (GCNs) have shown excellent performance in graph-structured tasks such as node classification and graph classification. However, recent research has shown that GCNs are vulnerable to a new type of threat called the backdoor attack, where the adversary can inject a hidden backdoor into the GCNs so that the backdoored model performs well on benign samples, whereas its prediction will be maliciously changed to the attacker-specified target label if the hidden backdoor is activated by the attacker-defined trigger. Clean-label backdoor attack and semantic backdoor attack are two new backdoor attacks to Deep Neural Networks (DNNs), they are more imperceptible and have posed new and serious threats. The semantic and clean-label backdoor attack is not fully explored in GCNs. In this paper, we propose a semantic and clean-label backdoor attack against GCNs under the context of graph classification to reveal the existence of this security vulnerability in GCNs. Specifically, SCLBA conducts an importance analysis on graph samples to select one type of node as semantic trigger, which is then inserted into the graph samples to create poisoning samples without changing the labels of the poisoning samples to the attacker-specified target label. We evaluate SCLBA on multiple datasets and the results show that SCLBA can achieve attack success rates close to 99% with poisoning rates of less than 3%, and with almost no impact on the performance of model on benign samples.
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