曲美替尼
mTORC1型
西罗莫司
MAPK/ERK通路
药物重新定位
药理学
生物
MEK抑制剂
癌症研究
医学
药品
内科学
信号转导
PI3K/AKT/mTOR通路
细胞生物学
作者
Lisonia Gkioni,Tobias Nespital,Maarouf Baghdadi,Carolina Monzó,Jitin Bali,Taim Nassr,Anna Lena Cremer,Andreas Beyer,Joris Deelen,Heiko Backes,Sebastian Grönke,Linda Partridge
出处
期刊:Nature Aging
[Nature Portfolio]
日期:2025-05-28
卷期号:5 (7): 1249-1265
被引量:29
标识
DOI:10.1038/s43587-025-00876-4
摘要
Suppression of the insulin-IGF-mTORC1-Ras network ameliorates aging in animals. Many drugs have targets in the network because of its roles in cancer and metabolic disease and are candidates for repurposing as geroprotectors. Rapamycin, an established geroprotective drug, blocks mTORC1 signaling, and trametinib inhibits the Ras-MEK-ERK pathway. In this study, we assessed survival and health of male and female mice treated with trametinib, rapamycin or their combination. We show here that trametinib treatment extended lifespan in both sexes and that its combination with rapamycin was additive. Combination treatment reduced liver tumors in both sexes and spleen tumors in male mice, blocked the age-related increase in brain glucose uptake and strongly reduced inflammation in brain, kidney, spleen and muscle and circulating levels of pro-inflammatory cytokines. We conclude that trametinib is a geroprotector in mice and that its combination with rapamycin is more effective than either drug alone, making the combination a candidate for repurposing as a gerotherapy in humans.
科研通智能强力驱动
Strongly Powered by AbleSci AI