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Effects of aerobic training on oxidative status in postsurgical non-small cell lung cancer patients: a pilot study.

Publication ,  Journal Article
Jones, LW; Eves, ND; Spasojevic, I; Wang, F; Il'yasova, D
Published in: Lung Cancer
April 2011

BACKGROUND: Oxidative stress is postulated to contribute to the initiation, promotion, and progression of non-small cell lung cancer (NSCLC). We investigated the effects of supervised, moderate-intensity aerobic training on urinary markers of oxidative status in patients with postsurgical NSCLC. PATIENTS AND METHODS: Sixteen patients with histologically confirmed stage I-IIIB NSCLC were recruited. Exercise training consisted of aerobic cycle ergometry sessions at 60 to ≥70% of baseline peak workload 20-45 min·d(-1), 3 d·wk(-1)for 14 weeks. Oxidative status was assessed via four urinary F(2)-isoprostanes isomers: iPF (2-alpha)-III, 2,3-dinor-iPF(2 alpha)-III, iPF (2-alpha)-VI, and 8,12-iso-iPF(2 alpha)-VI using liquid chromatography with tandem mass spectrometry detection. Peak oxygen consumption (VO2peak) was assessed using a maximal, incremental, cardiopulmonary exercise test with expired gas analysis. RESULTS: A composite index of all four F2-isoprostanes isomers increased from baseline to post-intervention by 32% (p = 0.08). Concerning individual isomers, iPF (2-alpha)-III increased by 0.09 (+55%; p = .010), iPF (2-alpha)-VI by 0.81 (+29%; p = 0.04), and 8,12-iso-iPF(2 alpha)-VI by 0.59 (+28%; p = 0.07) from baseline to postintervention. There was no change in 2,3-dinor-iPF(2 alpha)-III levels. VO2peak increased 1.1 mL·kg·(-1) min(-1) (p = 0.14) and peak workload increased 10 Watts (p < .001). Change in VO2peak was not associated with change in markers of oxidative status. CONCLUSIONS: Aerobic training was associated with significant increases in urinary measures of oxidative status in postsurgical NSCLC. The clinical implications of these findings are currently unknown. Further studies are required to elucidate the complex relationship between aerobic training, oxidative stress, tumor biology, and response to cytotoxic agents in mouse and human models of cancer.

Duke Scholars

Published In

Lung Cancer

DOI

EISSN

1872-8332

Publication Date

April 2011

Volume

72

Issue

1

Start / End Page

45 / 51

Location

Ireland

Related Subject Headings

  • Postoperative Period
  • Pilot Projects
  • Oxygen Consumption
  • Oxidative Stress
  • Oncology & Carcinogenesis
  • Middle Aged
  • Male
  • Lung Neoplasms
  • Humans
  • Female
 

Citation

APA
Chicago
ICMJE
MLA
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Jones, L. W., Eves, N. D., Spasojevic, I., Wang, F., & Il’yasova, D. (2011). Effects of aerobic training on oxidative status in postsurgical non-small cell lung cancer patients: a pilot study. Lung Cancer, 72(1), 45–51. https://doi.org/10.1016/j.lungcan.2010.08.002
Jones, Lee W., Neil D. Eves, Ivan Spasojevic, Frances Wang, and Dora Il’yasova. “Effects of aerobic training on oxidative status in postsurgical non-small cell lung cancer patients: a pilot study.Lung Cancer 72, no. 1 (April 2011): 45–51. https://doi.org/10.1016/j.lungcan.2010.08.002.
Jones LW, Eves ND, Spasojevic I, Wang F, Il’yasova D. Effects of aerobic training on oxidative status in postsurgical non-small cell lung cancer patients: a pilot study. Lung Cancer. 2011 Apr;72(1):45–51.
Jones, Lee W., et al. “Effects of aerobic training on oxidative status in postsurgical non-small cell lung cancer patients: a pilot study.Lung Cancer, vol. 72, no. 1, Apr. 2011, pp. 45–51. Pubmed, doi:10.1016/j.lungcan.2010.08.002.
Jones LW, Eves ND, Spasojevic I, Wang F, Il’yasova D. Effects of aerobic training on oxidative status in postsurgical non-small cell lung cancer patients: a pilot study. Lung Cancer. 2011 Apr;72(1):45–51.
Journal cover image

Published In

Lung Cancer

DOI

EISSN

1872-8332

Publication Date

April 2011

Volume

72

Issue

1

Start / End Page

45 / 51

Location

Ireland

Related Subject Headings

  • Postoperative Period
  • Pilot Projects
  • Oxygen Consumption
  • Oxidative Stress
  • Oncology & Carcinogenesis
  • Middle Aged
  • Male
  • Lung Neoplasms
  • Humans
  • Female