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体育活动可延缓小鼠肥胖相关的胰腺导管腺癌发展并减轻炎症。

Physical Activity Delays Obesity-Associated Pancreatic Ductal Adenocarcinoma in Mice and Decreases Inflammation.

作者信息

Pita-Grisanti Valentina, Dubay Kelly, Lahooti Ali, Badi Niharika, Ueltschi Olivia, Gumpper-Fedus Kristyn, Hsueh Hsiang-Yin, Lahooti Ila, Chavez-Tomar Myrriah, Terhorst Samantha, Knoblaugh Sue E, Cao Lei, Huang Wei, Coss Christopher C, Mace Thomas A, Choueiry Fouad, Hinton Alice, Mitchell Jennifer M, Schmandt Rosemarie, Grinsfelder Michaela Onstad, Basen-Engquist Karen, Cruz-Monserrate Zobeida

机构信息

Department of Internal Medicine, Division of Gastroenterology, Hepatology, and Nutrition, The Ohio State University Wexner Medical Center, Columbus, OH.

The Comprehensive Cancer Center-Arthur G. James Cancer Hospital and Richard J. Solove Research Institute, The Ohio State University, Columbus, OH.

出版信息

bioRxiv. 2023 Jan 4:2023.01.03.521203. doi: 10.1101/2023.01.03.521203.

Abstract

BACKGROUND & AIMS: Obesity is a risk factor for pancreatic ductal adenocarcinoma (PDAC), a deadly disease with limited preventive strategies. Lifestyle interventions to decrease obesity might prevent obesity-associated PDAC. Here, we examined whether decreasing obesity by increased physical activity (PA) and/or dietary changes would decrease inflammation in humans and prevent PDAC in mice.

METHODS

Circulating inflammatory-associated cytokines of overweight and obese subjects before and after a PA intervention were compared. PDAC pre-clinical models were exposed to PA and/or dietary interventions after obesity-associated cancer initiation. Body composition, tumor progression, growth, fibrosis, inflammation, and transcriptomic changes in the adipose tissue were evaluated.

RESULTS

PA decreased the levels of systemic inflammatory cytokines in overweight and obese subjects. PDAC mice on a diet-induced obesity (DIO) and PA intervention, had delayed weight gain, decreased systemic inflammation, lower grade pancreatic intraepithelial neoplasia lesions, reduced PDAC incidence, and increased anti-inflammatory signals in the adipose tissue compared to controls. PA had additional cancer prevention benefits when combined with a non-obesogenic diet after DIO. However, weight loss through PA alone or combined with a dietary intervention did not prevent tumor growth in an orthotopic PDAC model. Adipose-specific targeting of interleukin (IL)-15, an anti-inflammatory cytokine induced by PA in the adipose tissue, slowed PDAC growth.

CONCLUSIONS

PA alone or combined with diet-induced weight loss delayed the progression of PDAC and reduced systemic and adipose inflammatory signals. Therefore, obesity management via dietary interventions and/or PA, or modulating weight loss related pathways could prevent obesity-associated PDAC in high-risk obese individuals.

摘要

背景与目的

肥胖是胰腺导管腺癌(PDAC)的一个风险因素,这是一种致命疾病,预防策略有限。通过生活方式干预减轻肥胖可能预防与肥胖相关的PDAC。在此,我们研究了通过增加体力活动(PA)和/或饮食改变来减轻肥胖是否会减轻人类炎症并预防小鼠的PDAC。

方法

比较超重和肥胖受试者在PA干预前后循环中与炎症相关的细胞因子。在肥胖相关癌症发生后,将PDAC临床前模型暴露于PA和/或饮食干预。评估身体组成、肿瘤进展、生长、纤维化、炎症以及脂肪组织中的转录组变化。

结果

PA降低了超重和肥胖受试者全身炎症细胞因子的水平。与对照组相比,饮食诱导肥胖(DIO)和PA干预的PDAC小鼠体重增加延迟、全身炎症减轻、胰腺上皮内瘤变病变级别降低、PDAC发病率降低,且脂肪组织中的抗炎信号增加。在DIO后,PA与非致肥胖饮食联合使用时具有额外的癌症预防益处。然而,单独通过PA或与饮食干预联合进行的体重减轻并不能预防原位PDAC模型中的肿瘤生长。对脂肪组织中由PA诱导的抗炎细胞因子白细胞介素(IL)-15进行脂肪特异性靶向,减缓了PDAC的生长。

结论

单独的PA或与饮食诱导的体重减轻相结合可延缓PDAC的进展,并减少全身和脂肪的炎症信号。因此,通过饮食干预和/或PA进行肥胖管理,或调节与体重减轻相关的途径,可以预防高危肥胖个体中与肥胖相关的PDAC。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6415/9881853/6f6209028254/nihpp-2023.01.03.521203v1-f0002.jpg

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