Ectopic expression of guanylyl cyclase C in CD34(+) progenitor cells in peripheral blood

Purpose: To examine the utility of guanylyl cyclase C (GC-C)-specific neste d reverse transcriptase polymerase chain reaction (RT-PCR) to detect circul ating tumor cells in patients with colorectal cancer. Patients and Methods: Peripheral-blood mononuclear cells from 24 patients w ith Dukes' stage D colorectal cancer were analyzed by GC-C-specific nested RT-PCR using 1 mug of total RNA. Peripheral-blood mononuclear cells from 20 healthy volunteers served as controls. Additionally, peripheral-blood CD34 (+) progenitor cells were assayed for the expression of both GC-C and other epithelial cell-specific markers. Results: GC-C mRNA was detected in blood mononuclear cells from all 24 pati ents with colorectal cancer and all healthy volunteers. These unexpected po sitive results reflected low-level ectopic transcription of GC-C in CD34(+) progenitor cells. Moreover, CD34(+) progenitor cells expressed other epith elial cell-specific markers, including prostate-specific antigen, prostate- specific membrane antigen, carcinoembryonic antigen, CK-19, CK-20, mucin 1, and GA733.2. Limiting the quantity of mononuclear cell total RNA analyzed to less than or equal to 0.8 mug eliminated detection of GC-C and other tis sue-specific transcripts in blood of healthy volunteers. However, under the same conditions, GC-C mRNA was detected in mononuclear cells from all 24 p atients with metastatic colorectal cancer. Using 0.5 mug of total RNA and G C-C-specific primers, nested RT-PCR detected a single human colon carcinoma cell (approximately 20 to 200 GC-C transcripts/cell) in 10(6) to 10(7) mon onuclear blood cells. Conclusion: These data suggest that GC-C may be useful for detecting circul ating colorectal cancer cells. They also demonstrate that CD34(+) cells are a source of ectopically expressed epithelial cell-specific markers and tha t CD34(+) cells may contribute to the high falsepositive rate generally obs erved when those markers are used to detect rare circulating metastatic can cer cells by RT-PCR. (C) 2001 by American Society of Clinical Oncology.