Cancer and Metastasis Reviews

, 26:525

Cyclooxygenases, prostanoids, and tumor progression


DOI: 10.1007/s10555-007-9096-5

Cite this article as:
Wang, MT., Honn, K.V. & Nie, D. Cancer Metastasis Rev (2007) 26: 525. doi:10.1007/s10555-007-9096-5


In response to various growth factors, hormones or cytokines, arachidonic acid can be mobilized from phospholipids pools and converted to bioactive eicosanoids through cyclooxygenase (COX), lipoxygenase (LOX) or P-450 epoxygenase pathway. The COX pathway generates five major prostanoids (prostaglandin D2, prostaglandin E2, prostaglandin F, prostaglandin I2 and thromboxane A2) that play important roles in diverse biological processes. Studies suggest that different prostanoids and their own synthase can play distinct roles in tumor progression and cancer metastasis. COX-2 and PGE2 synthase have been most well documented in the regulation of various aspects of tumor progression and metastasis. PGE2, for example, can stimulate angiogenesis or other signaling pathways by binding to its receptors termed EPs. Therefore, targeting downstream prostanoids may provide a new avenue to impede tumor progression. In this review, aberrant expression and functions of several prostanoid synthetic enzymes in cancer will be discussed. The possible regulation of tumor progression by prostaglandins and their receptors will also be discussed.


Cyclooxygenase Prostanoids Tumor progression Metastasis 

Copyright information

© Springer Science+Business Media, LLC 2007

Authors and Affiliations

  1. 1.Department of Medical Microbiology, Immunology, and Cell BiologySouthern Illinois University School of Medicine and Cancer InstituteSpringfieldUSA
  2. 2.Department of PathologyWayne State University School of MedicineDetroitUSA

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