Apolipoprotein A-I reverse transcriptase-polymerase chain reaction analysis for detection of hematogenous colon cancer dissemination

Int J Oncol. 1998 Sep;13(3):443-7. doi: 10.3892/ijo.13.3.443.

Abstract

Detection of systemic tumor dissemination in colon carcinoma patients might be important for selection of appropriate treatment modalities. It has been previously shown that Apolipoprotein A-I (Apo A-I) is expressed in human intestinal epithelial cells, and in some human colon carcinoma cell lines. We examined the expression of Apo A-I mRNA in 14 human primary colon carcinomas by Northern blot and/or reverse transcriptase-polymerase chain reaction (RT-PCR) analysis. An Apo A-I specific transcript was found in up to 70% of the colon carcinomas. We developed an RT-PCR assay for Apo A-I transcripts, to identify circulating carcinoma cells in the peripheral blood of colon cancer patients. The Apo A-I RT-PCR assay was optimized using limiting dilution of an Apo A-I positive cancer cell line mixed with peripheral blood from healthy donor. In this system, up to 10 colon carcinoma cells were detected in 5 ml of peripheral blood. We examined Apo A-I mRNA expression in peripheral blood samples from 4 healthy donors, 20 colon carcinoma patients, and 11 individuals with tumor disease other than colon cancer. No Apo A-I mRNA was detected in the healthy donors and in the patients without colon cancer. Two out of 10 patients with metastatic colon carcinoma were positive by this assay, whereas Apo A-I mRNA was not found in any of the blood samples from the 10 radically resected colon carcinoma patients. These data suggest that Apo A-I RT-PCR assay is a highly specific and sensitive assay, although a low number of advanced colon carcinoma patients was found to be positive.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apolipoprotein A-I / biosynthesis*
  • Blotting, Northern
  • Caco-2 Cells / metabolism
  • Colon / metabolism
  • Colonic Neoplasms / blood*
  • Colonic Neoplasms / metabolism*
  • Colonic Neoplasms / pathology
  • DNA, Neoplasm / genetics
  • Humans
  • Intestinal Mucosa / metabolism
  • Neoplastic Cells, Circulating / metabolism*
  • Polymerase Chain Reaction
  • RNA, Messenger / blood*
  • RNA, Messenger / metabolism*
  • Transcription, Genetic

Substances

  • Apolipoprotein A-I
  • DNA, Neoplasm
  • RNA, Messenger