Molecular Carcinogenesis Program, Brazilian National Cancer Institute (INCA), Rio de Janeiro, RJ, Brazil.
Department of Physical Education, State University of Londrina, Londrina, PR, Brazil.
Anticancer Res. 2024 Mar;44(3):1209-1217. doi: 10.21873/anticanres.16916.
BACKGROUND/AIM: High-intensity interval training (HIIT) can trigger transient anti-tumor cytotoxicity through the mobilization of natural killer cells (NK cells) and myokines. Yet, the effects of HIIT on tumor development and microenvironment are unclear.
Male C57/BL6 mice were administered either MC38 of syngeneic colon cancer cells or vehicle in a single subcutaneous injection. Before injection, the training group completed four weeks of the HIIT program (progressive swimming training, 3/week, 10-12 min, 4-6% of body weight for overload). Following injection, trained mice continued to exercise for two additional weeks.
Pre and post-HIIT training was effective in preventing tumor onset (p=0.0065), maintaining body weight gain, and counteracting splenomegaly by 40% compared to the tumor group. However, HIIT had no impact on suppressing tumor growth, modifying final tumor volume, or significantly changing tumor proliferation (Ki-67), connective tissue content, or DNA double-strand damage detected by phospho-histone gamma-H2AX (γ-H2AX).
Pre and post-HIIT program is feasible for mice carrying a subcutaneous syngeneic tumor and effective in delaying tumor burden; however, HIIT did not alter colon tumor endpoints.
背景/目的:高强度间歇训练(HIIT)可以通过动员自然杀伤细胞(NK 细胞)和肌因子来引发短暂的抗肿瘤细胞毒性。然而,HIIT 对肿瘤发展和微环境的影响尚不清楚。
雄性 C57/BL6 小鼠经单次皮下注射 MC38 同源结肠癌细胞或载体。在注射前,训练组完成了四周的 HIIT 方案(渐进式游泳训练,每周 3 次,每次 10-12 分钟,体重的 4-6%为过载)。注射后,训练组的小鼠继续进行两周的额外运动。
HIIT 训练无论是在预防肿瘤发生(p=0.0065)、维持体重增加,还是对抗肿瘤组的脾肿大 40%方面都非常有效。然而,HIIT 对抑制肿瘤生长、改变最终肿瘤体积或显著改变肿瘤增殖(Ki-67)、结缔组织含量或磷酸组蛋白γ-H2AX(γ-H2AX)检测到的 DNA 双链断裂没有影响。
HIIT 方案在携带皮下同源肿瘤的小鼠中是可行的,并且可以有效延迟肿瘤负担;然而,HIIT 并没有改变结肠肿瘤终点。