4.3 Article

Tumor vessel normalization after aerobic exercise enhances chemotherapeutic efficacy

期刊

ONCOTARGET
卷 7, 期 40, 页码 65429-65440

出版社

IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.11748

关键词

tumor vascular normalization; NFAT; thrombospondin-1; exercise

资金

  1. National Cancer Institute of National Institutes of Health [T32CA009140]
  2. American Heart Association Post-Doctoral Fellowship [14POST20450102]
  3. National Institutes of Health [R01EB00262, R01HL115553, R01CA118374]
  4. Garrett B. Smith Foundation
  5. TedDriyen Foundation
  6. [U54-CA155850]

向作者/读者索取更多资源

Targeted therapies aimed at tumor vasculature are utilized in combination with chemotherapy to improve drug delivery and efficacy after tumor vascular normalization. Tumor vessels are highly disorganized with disrupted blood flow impeding drug delivery to cancer cells. Although pharmacologic anti-angiogenic therapy can remodel and normalize tumor vessels, there is a limited window of efficacy and these drugs are associated with severe side effects necessitating alternatives for vascular normalization. Recently, moderate aerobic exercise has been shown to induce vascular normalization in mouse models. Here, we provide a mechanistic explanation for the tumor vascular normalization induced by exercise. Shear stress, the mechanical stimuli exerted on endothelial cells by blood flow, modulates vascular integrity. Increasing vascular shear stress through aerobic exercise can alter and remodel blood vessels in normal tissues. Our data in mouse models indicate that activation of calcineurin-NFAT-TSP1 signaling in endothelial cells plays a critical role in exercise-induced shear stress mediated tumor vessel remodeling. We show that moderate aerobic exercise with chemotherapy caused a significantly greater decrease in tumor growth than chemotherapy alone through improved chemotherapy delivery after tumor vascular normalization. Our work suggests that the vascular normalizing effects of aerobic exercise can be an effective chemotherapy adjuvant.

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