Yuan Tanwei, Tagscherer Katrin E, Roth Wilfried, Bewerunge-Hudler Melanie, Brobeil Alexander, Kloor Matthias, Bläker Hendrik, Brenner Hermann, Hoffmeister Michael
Division of Clinical Epidemiology and Aging Research, Molecular Pathological Epidemiology Group, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 581, 69120, Heidelberg, Germany.
Medical Faculty Heidelberg, Heidelberg University, Heidelberg, Germany.
Clin Epigenetics. 2025 Jul 3;17(1):113. doi: 10.1186/s13148-025-01918-9.
Smoking is a well-established risk factor for colorectal cancer (CRC) development. However, the reliability of DNA methylation-based smoking signatures in predicting smoking status and their prognostic value in CRC remain unclear, particularly across different biological sample types.
Five previously validated methylation-based smoking signatures were analyzed in 2237 CRC patients with blood-derived DNA and 2273 patients with tumor tissue-derived DNA. Blood-derived signatures showed strong correlations with self-reported smoking status, effectively differentiating current smokers from never smokers (all p < 0.0001), with excellent discriminative ability (median area under the receiver operating characteristic curve: 0.94). In contrast, tumor tissue-derived signatures exhibited much weaker associations with smoking status. Among non-metastatic CRC patients, blood-derived methylation signatures were significantly associated with increased risks of all-cause and non-CRC-related mortality, but not with CRC-specific mortality. Conversely, two tumor tissue-derived signatures demonstrated stronger associations with CRC-specific mortality compared to blood-derived signatures.
Blood-derived methylation-based smoking signatures are robust indicators for smoking exposure and are associated with increased mortality risk among non-metastatic CRC patients. When applied to tumor tissue, signatures showed stronger associations with CRC-specific mortality.
吸烟是结直肠癌(CRC)发生的一个已明确的危险因素。然而,基于DNA甲基化的吸烟特征在预测吸烟状态方面的可靠性及其在CRC中的预后价值仍不清楚,尤其是在不同生物样本类型中。
对2237例使用血液来源DNA的CRC患者和2273例使用肿瘤组织来源DNA的患者分析了五个先前验证的基于甲基化的吸烟特征。血液来源的特征与自我报告的吸烟状态显示出强相关性,能有效区分当前吸烟者和从不吸烟者(所有p < 0.0001),具有出色的判别能力(受试者操作特征曲线下面积中位数:0.94)。相比之下,肿瘤组织来源的特征与吸烟状态的关联要弱得多。在非转移性CRC患者中,血液来源的甲基化特征与全因和非CRC相关死亡率的增加风险显著相关,但与CRC特异性死亡率无关。相反,与血液来源的特征相比,两个肿瘤组织来源的特征与CRC特异性死亡率的关联更强。
基于血液甲基化的吸烟特征是吸烟暴露的可靠指标,并且与非转移性CRC患者的死亡率增加风险相关。当应用于肿瘤组织时,特征与CRC特异性死亡率的关联更强。