胃饥饿素诱导的神经元神经肽Y促进低体重指数肺癌患者的脑转移。
Ghrelin-induced neuronal NPY promotes brain metastasis in lung cancer patients with low BMI.
作者信息
Tyagi Abhishek, Wu Shih-Ying, Kim Jee-Won, Deshpande Ravindra Pramod, Wu Kerui, Smith Eleanor C, Banna Giuseppe L, Watabe Kounosuke
机构信息
Department of Cancer Biology, Wake Forest University School of Medicine, Winston-Salem, NC, 27157, USA.
Nanoscience Department, Joint School of Nanoscience & Nanoengineering, Greensboro, NC, 27401, USA.
出版信息
Nat Commun. 2025 Jul 1;16(1):5608. doi: 10.1038/s41467-025-60730-4.
Obesity is a known risk factor for many cancers, yet recent studies reveal a paradoxical association between low body mass index (BMI) and increased brain metastasis in lung cancer-referred to as the "obesity paradox," with unclear molecular mechanism(s). Here, we show a significantly higher incidence of brain metastasis in low-BMI lung cancer patients compared to those with high-BMI or other cancer brain metastasis in a pan-analysis of 7628 patients. Mechanistically, low BMI activates ghrelin-GHSR signaling, increasing neuronal neuropeptide Y (NPY) secretion, which promotes tumor metabolic reprogramming via NPY-Y5R, facilitating brain colonization. Elevated plasma ghrelin levels in cancer-free low-BMI subjects suggest its potential as a prognostic biomarker for predicting brain metastasis. Notably, targeting NPY-Y5R or reversing low BMI effectively suppresses brain metastasis, supporting its pro-metastatic role. These findings provide a strong rationale for developing targeted interventions to treat or prevent brain metastasis in lung cancer patients with low BMI.
肥胖是许多癌症已知的风险因素,但最近的研究揭示了低体重指数(BMI)与肺癌脑转移增加之间存在矛盾的关联,即所谓的“肥胖悖论”,其分子机制尚不清楚。在这里,我们在对7628例患者的全分析中发现,低BMI肺癌患者的脑转移发生率显著高于高BMI患者或其他癌症脑转移患者。从机制上讲,低BMI激活胃饥饿素-GHSR信号通路,增加神经元神经肽Y(NPY)分泌,后者通过NPY-Y5R促进肿瘤代谢重编程,从而促进脑转移灶形成。无癌低BMI受试者血浆胃饥饿素水平升高表明其作为预测脑转移的预后生物标志物的潜力。值得注意的是,靶向NPY-Y5R或逆转低BMI可有效抑制脑转移,支持其促转移作用。这些发现为开发针对性干预措施以治疗或预防低BMI肺癌患者的脑转移提供了有力依据。