Li Ying, Chen Zihan, Huang Zongwei, Wang Jing, Wang Jue, Lin Lanxin, Lin Ruyu, Lai Jinghua, Zhang Libin, Qiu Sufang
Clinical Oncology School of Fujian Medical University, Fujian Cancer Hospital, Fuzhou, 350014, Fujian, China.
Fujian Medical University, Fujian, China.
Hereditas. 2025 Mar 14;162(1):36. doi: 10.1186/s41065-025-00408-5.
Blood metabolites play an important role in predicting or influencing the occurrence and development of cancers. We aimed to evaluate the relationship between blood metabolites and the occurrence of head and neck cancer (HNC).
We employed a Mendelian randomization (MR) approach to investigate the role of blood metabolites in HNC predisposition. The HNC cell line HN30 was treated with butyrylcarnitine, the metabolite identified through MR analysis, and subjected to a series of cellular assays to assess its potential carcinogenic effects.
Among the 258 blood metabolites analyzed, butyrylcarnitine emerged as the only metabolite demonstrating a potential causal association with HNC risk following Bonferroni correction (inverse-variance-weighted MR method: β = 0.904, P < 0.001). Genetically predicted higher levels of butyrylcarnitine (log-transformed) were causally linked to an increased risk of HNC (OR: 2.470, 95% CI: 1.530-3.987). Sensitivity analyses, including MR-Egger regression, leave-one-out analysis, and funnel plots, confirmed the robustness of the findings, with no evidence of directional pleiotropy. In vitro experiments further demonstrated that butyrylcarnitine promoted the proliferation, migration and invasion of HN30 cells.
By employing a genetic epidemiological framework, our research assessed the impact of metabolite butyrylcarnitine on HNC susceptibility. These findings offer valuable insights into potential therapeutic targets and highlight the promise of targeted metabolic strategies for reducing HNC risk. Nevertheless, further research is required to elucidate the precise biological mechanisms underlying these findings.
血液代谢物在预测或影响癌症的发生和发展中起着重要作用。我们旨在评估血液代谢物与头颈癌(HNC)发生之间的关系。
我们采用孟德尔随机化(MR)方法来研究血液代谢物在HNC易感性中的作用。用通过MR分析确定的代谢物丁酰肉碱处理HNC细胞系HN30,并进行一系列细胞试验以评估其潜在的致癌作用。
在分析的258种血液代谢物中,经Bonferroni校正后,丁酰肉碱是唯一显示出与HNC风险存在潜在因果关联的代谢物(逆方差加权MR方法:β = 0.904,P < 0.001)。遗传预测的较高水平的丁酰肉碱(对数转换)与HNC风险增加存在因果关系(OR:2.470,95% CI:1.530 - 3.987)。敏感性分析,包括MR-Egger回归、留一法分析和漏斗图,证实了研究结果的稳健性,没有方向性多效性的证据。体外实验进一步表明,丁酰肉碱促进了HN30细胞的增殖、迁移和侵袭。
通过采用遗传流行病学框架,我们的研究评估了代谢物丁酰肉碱对HNC易感性的影响。这些发现为潜在的治疗靶点提供了有价值的见解,并突出了靶向代谢策略在降低HNC风险方面的前景。然而,需要进一步的研究来阐明这些发现背后的确切生物学机制。