Identification of carcinoembryonic antigen-producing cells circulating in the blood of patients with colorectal carcinoma by reverse transcriptase polymerase chain reaction
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Jonas, S
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CHELSEA & WESTMINSTER HOSP,CHARING CROSS & WESTMINSTER MED SCH,DEPT SURG,LONDON SW10 9NH,ENGLANDCHELSEA & WESTMINSTER HOSP,CHARING CROSS & WESTMINSTER MED SCH,DEPT SURG,LONDON SW10 9NH,ENGLAND
Jonas, S
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Windeatt, S
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CHELSEA & WESTMINSTER HOSP,CHARING CROSS & WESTMINSTER MED SCH,DEPT SURG,LONDON SW10 9NH,ENGLANDCHELSEA & WESTMINSTER HOSP,CHARING CROSS & WESTMINSTER MED SCH,DEPT SURG,LONDON SW10 9NH,ENGLAND
Windeatt, S
[1
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OBoateng, A
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CHELSEA & WESTMINSTER HOSP,CHARING CROSS & WESTMINSTER MED SCH,DEPT SURG,LONDON SW10 9NH,ENGLANDCHELSEA & WESTMINSTER HOSP,CHARING CROSS & WESTMINSTER MED SCH,DEPT SURG,LONDON SW10 9NH,ENGLAND
OBoateng, A
[1
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Fordy, C
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CHELSEA & WESTMINSTER HOSP,CHARING CROSS & WESTMINSTER MED SCH,DEPT SURG,LONDON SW10 9NH,ENGLANDCHELSEA & WESTMINSTER HOSP,CHARING CROSS & WESTMINSTER MED SCH,DEPT SURG,LONDON SW10 9NH,ENGLAND
Fordy, C
[1
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AllenMersh, TG
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CHELSEA & WESTMINSTER HOSP,CHARING CROSS & WESTMINSTER MED SCH,DEPT SURG,LONDON SW10 9NH,ENGLANDCHELSEA & WESTMINSTER HOSP,CHARING CROSS & WESTMINSTER MED SCH,DEPT SURG,LONDON SW10 9NH,ENGLAND
AllenMersh, TG
[1
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[1] CHELSEA & WESTMINSTER HOSP,CHARING CROSS & WESTMINSTER MED SCH,DEPT SURG,LONDON SW10 9NH,ENGLAND
Background-Application of the reverse transcriptase polymerase chain reaction (RT-PCR) to identification of circulating tumour cells in colorectal cancer. Aims-To assess whether circulating malignant cells in patients with colorectal liver metastasis could be identified by RT-PCR recognition of mRNA coding for the tumour marker carcinoembryonic antigen (CEA). Patients-A total of 31 with colorectal liver metastases and 22 no-cancer controls. Methods-Specific cDNA primers for CEA transcripts were used to apply RT-PCR to tissue biopsy specimens, colon carcinoma cell lines, and peripheral blood samples from patients with colorectal liver metastases. A strongly CEA-expressive HT115 colorectal carcinoma cell line was used to spike blood samples from no-cancer control subjects. Results-The limit for detection of CEA cDNA by Southern blotting using HT115 cells was 50 cells per 14 ml of spiked blood. There was a significant difference (p=0 . 007) in RT-PCR positive expression between patients with liver metastasis (26/31) compared with controls (5/22). There was no significant relation between the prevalence of CEA cDNA amplification and serum CEA level or metastasis volume in patients with liver metastasis. Conclusions-This is the first study to suggest that identification of circulating colorectal cancer cells using RT-PCR for detection of CEA cDNA is feasible.