肠促胰岛素三重激动剂利特鲁肽(LY3437943)缓解肥胖相关的癌症进展。

npj Metabolic Health and Disease Pub Date : 2025-01-01 Epub Date: 2025-03-14 DOI:10.1038/s44324-025-00054-5
Sandesh J Marathe, Emily W Grey, Margaret S Bohm, Sydney C Joseph, Arvind V Ramesh, Matthew A Cottam, Kamran Idrees, Kathryn E Wellen, Alyssa H Hasty, Jeffrey C Rathmell, Liza Makowski
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引用次数: 0

摘要

减肥的医学疗法正在改变肥胖的现状,但对肥胖相关癌症的影响仍不清楚。我们报道,在利特鲁肽(RETA, LY3437943)诱导体重减轻的临床前模型中,胰腺癌植入减少,肿瘤发病延迟,进展减弱,导致肿瘤体积减少14倍,而单激动剂semaglutide治疗小鼠仅减少4倍。尽管RETA停药后体重会再次增加,但RETA的抗肿瘤作用仍然存在。值得注意的是,reta诱导的保护作用扩展到肺癌模型,肿瘤植入减少50%,显著延迟肿瘤发作,减缓肿瘤进展,与对照组相比,肿瘤体积减少17倍。RETA诱导全身和肿瘤微环境中的免疫重编程,具有持久的抗肿瘤免疫,其证据是循环IL-6升高、抗原呈递细胞增加、免疫抑制细胞减少和促炎途径的激活。总之,我们的研究结果表明,reta介导的体重减轻患者也可能从降低癌症风险和改善预后中受益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Incretin triple agonist retatrutide (LY3437943) alleviates obesity-associated cancer progression.

Medical therapeutics for weight loss are changing the landscape of obesity but impacts on obesity-associated cancer remain unclear. We report that in pre-clinical models with significant retatrutide (RETA, LY3437943)-induced weight loss, pancreatic cancer engraftment was reduced, tumor onset was delayed, and progression was attenuated resulting in a 14-fold reduction in tumor volume compared to only 4-fold reduction in single agonist semaglutide-treated mice. Despite weight re-gain after RETA withdrawal, the anti-tumor benefits of RETA persisted. Remarkably, RETA-induced protection extends to a lung cancer model with 50% reduced tumor engraftment, significantly delayed tumor onset, and mitigated tumor progression, with a 17-fold reduction in tumor volume compared to controls. RETA induced immune reprogramming systemically and in the tumor microenvironment with durable anti-tumor immunity evidenced by elevated circulating IL-6, increased antigen presenting cells, reduced immunosuppressive cells, and activation of pro-inflammatory pathways. In sum, our findings suggest that patients with RETA-mediated weight loss may also benefit from reduced cancer risk and improved outcomes.

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