Circulating Prostaglandin Biosynthesis in Colorectal Cancer and Potential Clinical Significance

Haitao Li, Kangdong Liu, Lisa A. Boardman, Yuzhou Zhao, Lei Wang, Yuqiao Sheng, Naomi Oi, Paul J. Limburg, Ann M. Bode, Zigang Dong

Research output: Contribution to journalArticle

13 Scopus citations

Abstract

Background: Colorectal cancer (CRC) represents the third leading cause of cancer-related death in the United States. Lack of reliable biomarkers remains a critical issue for early detection of CRC. In this study, we investigated the potential predictive values of circulating prostaglandin (PG) biosynthesis in CRC risk. Methods: Profiles of circulating PG biosynthesis and platelet counts were determined in healthy subjects (n = 16), familial adenomatous polyposis (FAP) patients who were classified as regular aspirin users (n = 14) or nonusers (n = 24), and CRC patients with (n = 18) or without FAP history (n = 20). Immunohistochemistry staining was performed on biopsy samples. Results: Analysis of circulating PG biosynthesis unexpectedly revealed that CRC progression is accompanied by a pronounced elevation of circulating thromboxane A2 (TXA2) levels. When a circulating TXA2 level of 1000pg/mL was selected as a practical cutoff point, 95% of CRC patients were successfully identified. Further study suggested that the TXA2 pathway is constitutively activated during colorectal tumorigenesis and required for anchorage-independent growth of colon cancer cells. Conclusions: This study established the importance of the TXA2 pathway in CRC pathophysiology, and laid the groundwork for introducing a TXA2-targeting strategy to CRC prevention, early detection and management.

Original languageEnglish (US)
Pages (from-to)165-171
Number of pages7
JournalEBioMedicine
Volume2
Issue number2
DOIs
StatePublished - Feb 2015

Keywords

  • Colorectal cancer
  • Familial adenomatous polyposis
  • Thromboxane A

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)

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