Scholarlink

Background <p>Lung cancer remains the leading cause of cancer-related mortality globally. Despite advancements in treatment, survival rates for advanced-stage disease remain suboptimal, emphasizing the need for novel prevention strategies. Oxidative stress (OS), resulting from an imbalance between reactive oxygen species (ROS) and antioxidants, is implicated in lung cancer pathogenesis. This study aimed to explore bidirectional causal relationships between genetically predicted oxidative stress injury biomarkers (OSIBs) and lung cancer risk using mendelian randomization (MR).</p> Methods <p>A two-sample bidirectional MR approach was used to assess causal effects of 16 OSIBs on lung cancer subtypes (small cell lung cancer, squamous cell carcinoma, and adenocarcinoma) and vice versa. Genetic data were derived from large-scale genome-wide association studies in European populations.</p> Results <p>MR analysis revealed significant associations. Higher albumin levels were associated with reduced adenocarcinoma risk (OR = 0.599, 95%CI: 0.369–0.974, <i>P</i> = 0.039). Elevated monounsaturated fatty acids levels were linked to an increased risk of squamous cell carcinoma (OR = 1.742, 95% CI: 1.095–2.772, <i>P</i> = 0.019). Increased lactate levels were positively associated with small cell lung cancer (OR = 4.565, 95% CI: 1.009–20.657, <i>P</i> = 0.049). Reverse MR analysis did not suggest causal effects of lung cancer on OSIBs.</p> Conclusion <p>These findings highlight the distinct roles of OSIBs in lung cancer risk and underscore oxidative stress's pivotal role in cancer development. Further research is needed to validate these biomarkers for early detection and preventive strategies.</p>

错误：搜索内容不能为空，请输入英文关键词
错误：关键词超出字数限制，请精简
高级检索

Deciphering bidirectional causal links between oxidative stress and lung cancer risk through Mendelian randomization

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2025年7月28日

查看全文
  • XueLian Chen,
  • JianRong Zeng,
  • FengYun Cao,
  • Jun Cai,
  • Xin Ma,
  • ChangYu Pu

摘要

Background

Lung cancer remains the leading cause of cancer-related mortality globally. Despite advancements in treatment, survival rates for advanced-stage disease remain suboptimal, emphasizing the need for novel prevention strategies. Oxidative stress (OS), resulting from an imbalance between reactive oxygen species (ROS) and antioxidants, is implicated in lung cancer pathogenesis. This study aimed to explore bidirectional causal relationships between genetically predicted oxidative stress injury biomarkers (OSIBs) and lung cancer risk using mendelian randomization (MR).

Methods

A two-sample bidirectional MR approach was used to assess causal effects of 16 OSIBs on lung cancer subtypes (small cell lung cancer, squamous cell carcinoma, and adenocarcinoma) and vice versa. Genetic data were derived from large-scale genome-wide association studies in European populations.

Results

MR analysis revealed significant associations. Higher albumin levels were associated with reduced adenocarcinoma risk (OR = 0.599, 95%CI: 0.369–0.974, P = 0.039). Elevated monounsaturated fatty acids levels were linked to an increased risk of squamous cell carcinoma (OR = 1.742, 95% CI: 1.095–2.772, P = 0.019). Increased lactate levels were positively associated with small cell lung cancer (OR = 4.565, 95% CI: 1.009–20.657, P = 0.049). Reverse MR analysis did not suggest causal effects of lung cancer on OSIBs.

Conclusion

These findings highlight the distinct roles of OSIBs in lung cancer risk and underscore oxidative stress's pivotal role in cancer development. Further research is needed to validate these biomarkers for early detection and preventive strategies.