| Literature DB >> 35660135 |
Emma Kurz1, Carolina Alcantara Hirsch2, Tanner Dalton3, Sorin Alberto Shadaloey1, Alireza Khodadadi-Jamayran4, George Miller5, Sumedha Pareek6, Hajar Rajaei7, Chirayu Mohindroo7, Seyda Baydogan7, An Ngo-Huang8, Nathan Parker9, Matthew H G Katz10, Maria Petzel11, Emily Vucic12, Florencia McAllister13, Keri Schadler6, Rafael Winograd14, Dafna Bar-Sagi15.
Abstract
Aerobic exercise is associated with decreased cancer incidence and cancer-associated mortality. However, little is known about the effects of exercise on pancreatic ductal adenocarcinoma (PDA), a disease for which current therapeutic options are limited. Herein, we show that aerobic exercise reduces PDA tumor growth, by modulating systemic and intra-tumoral immunity. Mechanistically, exercise promotes immune mobilization and accumulation of tumor-infiltrating IL15Rα+ CD8 T cells, which are responsible for the tumor-protective effects. In clinical samples, an exercise-dependent increase of intra-tumoral CD8 T cells is also observed. Underscoring the translational potential of the interleukin (IL)-15/IL-15Rα axis, IL-15 super-agonist (NIZ985) treatment attenuates tumor growth, prolongs survival, and enhances sensitivity to chemotherapy. Finally, exercise or NIZ985 both sensitize pancreatic tumors to αPD-1, with improved anti-tumor and survival benefits. Collectively, our findings highlight the therapeutic potential of an exercise-oncology axis and identify IL-15 activation as a promising treatment strategy for this deadly disease.Entities:
Keywords: IL-15; PD-1; T cell; checkpoint blockade; exercise; immunology; immunotherapy; pancreatic cancer; super-agonist
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Year: 2022 PMID: 35660135 PMCID: PMC9280705 DOI: 10.1016/j.ccell.2022.05.006
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 38.585