Meng Wei, Xu Rui, Miller Eric, Sun Xiaowei, Thurmond Jennifer, Webb Amy, McElroy Joseph, Palmer Joshua, DiCostanzo Dominic J, Zhang Shiqi, Yamaguchi Hisashi, Haque Saikh Jaharul, Zhu Jiangjiang, Chakravarti Arnab
Department of Radiation Oncology, The Ohio State University, Columbus, Ohio 43210, United States.
Department of Human Sciences, The Ohio State University, Columbus, Ohio 43210, United States.
J Proteome Res. 2025 Apr 4;24(4):1662-1671. doi: 10.1021/acs.jproteome.4c00529. Epub 2025 Mar 12.
Lung cancer stands as the leading cause of cancer-related death worldwide, impacting both men and women in the United States and beyond. Radiation therapy (RT) serves as a key treatment modality for various lung malignancies. Our study aims to systematically assess the prognosis and influence of RT on metabolic reprogramming in patients diagnosed with nonsmall-cell lung cancer (NSCLC) through longitudinal metabolic profiling. A cohort of 54 NSCLC patients underwent thoracic radiotherapy, with 96% receiving a total radiation dose ranging from 40 to 70 Gy, averaging 56.3 Gy. Blood biospecimens were collected before RT, during RT, and at the first follow-up after RT, with a total of 126 serum samples randomized for liquid chromatography-mass spectrometry (LC-MS) metabolomics analysis using a high-performance LC (HPLC)-Q-Exactive mass spectrometry system. Our results indicated that the serum metabolite coumarin derivatives prior to radiotherapy exhibited the strongest unfavorable outcome with overall survival in these NSCLC cases. The metabolites in the blood samples can reflect the responses during RT. Notably, over half of the metabolites (12/23) were found to be fatty acids in the longitudinal analysis. This pilot study indicated that metabolic profiling of biofluids from NSCLC patients undergoing RT has the potential to assess the patient outcomes during and after treatment.
肺癌是全球癌症相关死亡的主要原因,对美国及其他地区的男性和女性都有影响。放射治疗(RT)是各种肺部恶性肿瘤的关键治疗方式。我们的研究旨在通过纵向代谢谱分析,系统评估放射治疗对非小细胞肺癌(NSCLC)患者代谢重编程的预后和影响。一组54例NSCLC患者接受了胸部放疗,96%的患者接受的总辐射剂量为40至70 Gy,平均为56.3 Gy。在放疗前、放疗期间和放疗后的首次随访时采集血液生物标本,共126份血清样本随机用于使用高效液相色谱(HPLC)-Q-Exactive质谱系统的液相色谱-质谱(LC-MS)代谢组学分析。我们的结果表明,在这些NSCLC病例中,放疗前血清代谢物香豆素衍生物与总体生存的不良结局关联最强。血液样本中的代谢物可反映放疗期间的反应。值得注意的是,在纵向分析中发现超过一半的代谢物(12/23)为脂肪酸。这项初步研究表明,对接受放疗的NSCLC患者生物流体进行代谢谱分析有潜力评估治疗期间及治疗后的患者预后。