TY - JOUR
T1 - Blood-based RT-PCR assays of MN/CA9 or PSMA
T2 - Clinical application in renal cancer patients
AU - De La Taille, Alexandre
AU - Katz, Aaron
AU - Cao, Yichen
AU - McKiernan, James
AU - Buttyan, Ralph
AU - Burchardt, Martin
AU - Burchardt, Tatjana
AU - Hayek, Omar
AU - Olsson, Carl A.
AU - Chopin, Dominique K.
AU - Sawczuk, Ihor S.
N1 - Funding Information:
Supported by grant ROI CA 70769 from the National Cancer Institute, National Institutes of Health, by MSD Merck (Bourse AFU-MSD 1998, France), and by Ministère des Affaires Etrangères (Programme Lavoisier, France)
PY - 2000/9
Y1 - 2000/9
N2 - Objectives. To report a survey of blood-based RNAs obtained from common groups of control and renal cancer patients for expression of both MN/CA9 and prostate-specific membrane antigen (PSMA) messenger RNAs. Methods. Reverse transcription polymerase chain reaction (RT-PCR) assays for MN/CA9 and PSMA were performed on RNAs extracted from 81 blood samples (59 patients with renal cancer, 7 with benign tumors, and 15 control volunteers). The results of these assays were statistically analyzed to determine whether a positive result (individually or combined) correlates with any tumor characteristics. Results. Neither MN/CA9 nor PSMA amplification products were detected in the RNAs from peripheral blood samples of the 15 control volunteers and from the 7 patients with benign renal tumor (sensitivity 100%). MN/CA9 alone was detected in 11 (19%) of 59 samples and PSMA alone in 12 (20%) of 59 samples from patients with renal cancer. PSMA positivity was significantly correlated with vascular invasion of the primary tumor. Expression of one or both of these molecular tumor markers was detected in 21 (36%) of 59 renal cancer patients. When combined, the results of the MN/CA9 and PSMA RT-PCR tests were found to be highly associated with vascular invasion in nephrectomy specimens (sensitivity 67%, specificity 77%, odds ratio = 6.89, P = 0.002). Conclusions. Combination of RT-PCR assays for MN/CA9 and PSMA provides a sensitive blood test for molecular detection of clear cell carcinoma of the kidney and its potential for vascular invasion. Further testing of this assay will be required to evaluate its efficacy in the diagnosis, screening, and follow-up of patients with kidney cancer. (C) 2000 Elsevier Science Inc.
AB - Objectives. To report a survey of blood-based RNAs obtained from common groups of control and renal cancer patients for expression of both MN/CA9 and prostate-specific membrane antigen (PSMA) messenger RNAs. Methods. Reverse transcription polymerase chain reaction (RT-PCR) assays for MN/CA9 and PSMA were performed on RNAs extracted from 81 blood samples (59 patients with renal cancer, 7 with benign tumors, and 15 control volunteers). The results of these assays were statistically analyzed to determine whether a positive result (individually or combined) correlates with any tumor characteristics. Results. Neither MN/CA9 nor PSMA amplification products were detected in the RNAs from peripheral blood samples of the 15 control volunteers and from the 7 patients with benign renal tumor (sensitivity 100%). MN/CA9 alone was detected in 11 (19%) of 59 samples and PSMA alone in 12 (20%) of 59 samples from patients with renal cancer. PSMA positivity was significantly correlated with vascular invasion of the primary tumor. Expression of one or both of these molecular tumor markers was detected in 21 (36%) of 59 renal cancer patients. When combined, the results of the MN/CA9 and PSMA RT-PCR tests were found to be highly associated with vascular invasion in nephrectomy specimens (sensitivity 67%, specificity 77%, odds ratio = 6.89, P = 0.002). Conclusions. Combination of RT-PCR assays for MN/CA9 and PSMA provides a sensitive blood test for molecular detection of clear cell carcinoma of the kidney and its potential for vascular invasion. Further testing of this assay will be required to evaluate its efficacy in the diagnosis, screening, and follow-up of patients with kidney cancer. (C) 2000 Elsevier Science Inc.
UR - http://www.scopus.com/inward/record.url?scp=17044442506&partnerID=8YFLogxK
U2 - 10.1016/S0090-4295(00)00647-6
DO - 10.1016/S0090-4295(00)00647-6
M3 - Article
C2 - 10962301
AN - SCOPUS:17044442506
SN - 0090-4295
VL - 56
SP - 393
EP - 398
JO - Urology
JF - Urology
IS - 3
ER -