Nemkov Travis, Cendali Francesca, Dzieciatkowska Monika, Stephenson Daniel, Hansen Kirk C, Jankowski Catherine M, D'Alessandro Angelo, Marker Ryan J
Department of Biochemistry and Molecular Genetics, Anschutz Medical Campus, University of Colorado, Aurora, CO 80045, USA.
College of Nursing, University of Colorado, Aurora, CO 80045, USA.
Pathophysiology. 2024 Mar 20;31(1):166-182. doi: 10.3390/pathophysiology31010013.
To molecularly characterize the impact of exercise on mitigating neoadjuvant treatment (NAT)-induced physical decline in pancreatic ductal adenocarcinoma (PDAC) patients, a multi-omics approach was employed for the analysis of plasma samples before and after a personalized exercise intervention. Consisting of personalized aerobic and resistance exercises, this intervention was associated with significant molecular changes that correlated with improvements in lean mass, appendicular skeletal muscle index (ASMI), and performance in the 400-m walk test (MWT) and sit-to-stand test. These alterations indicated exercise-induced modulation of inflammation and mitochondrial function markers. This case study provides proof-of-principal application for multiomics-based assessments of supervised exercise, thereby supporting this intervention as a feasible and beneficial intervention for PDAC patients to potentially enhance treatment response and patient quality of life. The molecular changes observed here underscore the importance of physical activity in cancer treatment protocols, advocating for the development of accessible multiomics-guided exercise programs for cancer patients.
为了从分子层面表征运动对减轻胰腺导管腺癌(PDAC)患者新辅助治疗(NAT)引起的身体机能衰退的影响,我们采用了多组学方法分析个性化运动干预前后的血浆样本。该干预包括个性化有氧运动和抗阻运动,与显著的分子变化相关,这些变化与瘦体重、四肢骨骼肌指数(ASMI)的改善以及400米步行测试(MWT)和坐立测试的表现相关。这些改变表明运动诱导了炎症和线粒体功能标志物的调节。本案例研究为基于多组学的监督运动评估提供了原理验证应用,从而支持这种干预作为一种可行且有益的干预措施,对PDAC患者可能增强治疗反应和提高生活质量。此处观察到的分子变化强调了身体活动在癌症治疗方案中的重要性,倡导为癌症患者开发可及的多组学指导运动项目。