Molecular Diagnostics
British Journal of Cancer (2007) 96, 1735–1739. doi:10.1038/sj.bjc.6603790 www.bjcancer.com
Published online 15 May 2007
Expression of IP-10 related to angiogenesis in uterine cervical cancers
E Sato1, J Fujimoto1, H Toyoki1, H Sakaguchi1, S M Alam1, I Jahan1 and T Tamaya1
1Department of Obstetrics and Gynecology, Gifu University School of Medicine, 1–1 Yanagido, Gifu City 501-1194, Japan
Correspondence: Associate Professor J Fujimoto, E-mail: jf@gifu-u.ac.jp
Received 8 December 2006; Revised 20 March 2007; Accepted 19 April 2007; Published online 15 May 2007.
Abstract
Angiogenesis is essential for development, growth and advancement of solid tumours. Interferon-
-inducible protein 10 (IP-10) regulates lymphocyte chemotaxis, mediates vascular pericyte proliferation and acts as an angiostatic agent, thus inhibiting tumour growth. This prompted us to study the clinical implications of IP-10 expression related to angiogenesis in uterine cervical cancers. The levels of IP-10 decreased with advancement, and the prognosis of the 30 patients with low IP-10 expression in uterine cervical cancers was poor (66%), whereas the 24-month survival rate of the other patients with high IP-10 expression was 90%. Furthermore, IP-10 levels significantly reverse-correlated with vascular endothelial growth factor (VEGF) levels in uterine cervical cancers. Interferon-
-inducible protein 10 might work on suppression of angiogenesis associated with VEGF in advancement, and can be recognised as a prognostic indicator. Furthermore, IP-10 activation might be effective on the suppression of regrowth or recurrence after intensive treatment for advanced cervical cancers.
Keywords:
IP-10, VEGF, angiogenesis, angiogenic inhibitor, uterine cervical cancer
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