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J Appl Physiol 103: 763-770, 2007. First published May 10, 2007; doi:10.1152/japplphysiol.00165.2007
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Exercise modulates platelet-nasopharyngeal carcinoma cell aggregation and subsequent tissue factor and matrix metalloproteinase activities

Jong-Shyan Wang,1 Chuen-Ying Chang,1 Shu-Er Chow,2 Yu-Wen Chen,1 and Chuen-Mao Yang3

1Graduate Institute of Rehabilitation Science and Center for Gerontological Research, and Departments of 2Physiology and 3Pharmacology, Chang Gung University, Tao-Yuan, Taiwan

Submitted 8 February 2007 ; accepted in final form 8 May 2007

Interaction between platelet and carcinoma cell contributes to pathogenesis of cancer-related thrombosis and metastasis. This study investigated whether physical exercise affects platelet-nasopharyngeal carcinoma cell (NPC) interaction and platelet-promoted tissue factor (TF) and matrix metalloproteinase (MMP) activities of NPC. Thirty sedentary men performed on three occasions moderate-intensity exercise [MIE, 60% maximal oxygen consumption (VO2max) for 40 min] and high-intensity exercise (HIE, up to VO2max), with and without warm-up exercise (WUE, 60% VO2max for 20 min) on a bicycle ergometer. Before and immediately after exercise, platelet-NPC aggregation, the TF, MMP-2 and MMP-9 expressions and activities, and TF pathway inhibitor (TFPI) and tissue inhibitor of MMP-1 levels of NPC and platelet were measured. The results of this study demonstrated that HIE enhanced platelet-NPC aggregation in the presence of fibrinogen and was accompanied by increased platelet-promoted TF activity, expression of NPC, decreased platelet-promoted MMP-2 and MMP-9 activities, and TFPI release of NPC, whereas these alterations to HIE on platelet-NPC interactions were ameliorated by WUE pretreatment. Conversely, MIE reduced the formation of platelet-NPC aggregates, but did not change the TF, TFPI, MMP-2, MMP-9, tissue inhibitor of MMP activities, and/or levels of NPC mediated by platelet. It is concluded that HIE may enhance aggregation and coagulation and reduce MMP bioactivity related to platelet-NPC interactions, by raising the binding affinity to fibrinogen and TF activity and expression and lowering TFPI release and MMP-2 and -9 activities. These effects on HIE diminish after WUE. However, MIE minimizes the risk of thrombosis induced by platelet-NPC interactions.

exercise intensity; tumor; cell interaction; thrombosis



Address for reprint requests and other correspondence: J. S. Wang, Graduate Institute of Rehabilitation Science, Chang Gung Univ., 259 Wen-Hwa 1st Rd., Kwei-Shan, Tao-Yuan 333, Taiwan (e-mail: s5492{at}mail.cgu.edu.tw)







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