Expression and significance of cyclooxygenase-2 mRNA in benign and malignant ascites

World J Gastroenterol. 2013 Oct 28;19(40):6883-7. doi: 10.3748/wjg.v19.i40.6883.

Abstract

Aim: To investigate the mRNA expression of cyclooxygensae-2 (COX-2) in benign and malignant ascites, and to explore the difference in COX-2 mRNA expression among different diseases.

Methods: A total of 36 samples were collected from the Fifth Affiliated Hospital of Sun Yat-Sen University and divided into two experimental groups: benign ascites (n = 21) and malignant ascites (n = 15). Benign ascites included cirrhotic ascites (n = 10) and tuberculous ascites (n = 5). Malignant ascites included oophoroma (n = 7), cancer of colon (n = 5), cancer of the liver (n = 6), gastric cancer (n = 2), and bladder carcinoma (n = 1). The mRNA expression of COX-2 in ascites was examined with reverse transcriptase polymerase chain reaction (RT-PCR) technology, and the positive rate of COX-2 mRNA was compared between different diseases.

Results: The positive rate of COX-2 mRNA in malignant ascites was 42.9% (9/21), which was significantly higher than in benign ascites, 6.7% (1/15), difference being significant between these two groups (χ(2) = 4.051, P = 0.044). The proportion of the positive rate in the malignant ascites was as follows: ovarian cancers 57.1% (4/7), colon cancer 40.0% (2/5), liver cancer 33.3% (2/6), gastric cancer 50.0% (1/2), and bladder cancer 0.00% (0/1). However, there was no significant difference in COX-2 mRNA expression among various tumors with malignant ascites (χ(2) = 1.614, P = 0.806). Among the benign ascites, COX-2 mRNA levels were different between the tuberculous ascites (0/5) and cirrhotic ascites (1/10), but there was no significant difference (P = 1.000).

Conclusion: COX-2 mRNA, detected by RT-PCR, is useful in the differential diagnosis of benign and malignant ascites, which also has potential value in the clinical diagnosis of tumors.

Keywords: Ascites; Cyclooxygensae-2 mRNA; Malignant tumor; Reverse transcriptase polymerase chain reaction.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Ascites / enzymology*
  • Ascites / genetics*
  • Ascites / microbiology
  • Biomarkers, Tumor / genetics*
  • Biopsy
  • Chi-Square Distribution
  • Cyclooxygenase 2 / genetics*
  • Diagnosis, Differential
  • Female
  • Gene Expression Regulation, Enzymologic
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Liver Cirrhosis / complications
  • Male
  • Middle Aged
  • Neoplasms / complications*
  • Predictive Value of Tests
  • RNA, Messenger / analysis*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Tuberculosis / complications

Substances

  • Biomarkers, Tumor
  • RNA, Messenger
  • Cyclooxygenase 2
  • PTGS2 protein, human