TY - JOUR
T1 - Quantification of Plasma β-Catenin mRNA in Colorectal Cancer and Adenoma Patients
AU - Wong, Sze Chuen Cesar
AU - Lo, Siu Fong Elena
AU - Cheung, Moon Tong
AU - Ng, Kai On Enders
AU - Tse, Chun Wah
AU - Lai, Bo San Paul
AU - Lee, King Chung
AU - Lo, Y. M Dennis
PY - 2004/3/1
Y1 - 2004/3/1
N2 - Purpose: Colorectal cancer is an important cause of cancer deaths. Here, we focused our investigation on the β-catenin gene which is implicated in colorectal carcinogenesis and tested whether β-catenin mRNA is detectable in the plasma of colorectal carcinoma and adenoma patients using quantitative reverse transcriptase-PCR. Experimental Design: Plasma β-catenin mRNA was measured from 58 colorectal carcinoma patients, 49 colorectal adenoma patients, and 43 apparently normal subjects using intron-spanning primers and Taqman probes. Five clinicopathological parameters were studied and correlated with plasma β-catenin mRNA concentration. Additionally, 19 colorectal carcinoma patients after tumor removal were also recruited for plasma β-catenin mRNA measurement to further demonstrate the clinical usefulness of this test. Results: β-catenin mRNA was detected with median concentrations of 8737 (range: 1480-933,100), 1218 (range: 541-2,254) and 291 (range: 0-1,366) copies/mi plasma in colorectal carcinoma, colorectal adenoma, and apparently normal subjects, respectively. Statistical analysis demonstrated that plasma β-catenin mRNA concentration was correlated to tumor stage but not sex, age, lymph node status, and degree in differentiation. Moreover, plasma β-catenin mRNA concentration decreased significantly after tumor removal in 16 of 19 (84%) colorectal carcinoma patients. Conclusions: We conclude that plasma β-catenin mRNA may potentially serve as a marker for colorectal cancer.
AB - Purpose: Colorectal cancer is an important cause of cancer deaths. Here, we focused our investigation on the β-catenin gene which is implicated in colorectal carcinogenesis and tested whether β-catenin mRNA is detectable in the plasma of colorectal carcinoma and adenoma patients using quantitative reverse transcriptase-PCR. Experimental Design: Plasma β-catenin mRNA was measured from 58 colorectal carcinoma patients, 49 colorectal adenoma patients, and 43 apparently normal subjects using intron-spanning primers and Taqman probes. Five clinicopathological parameters were studied and correlated with plasma β-catenin mRNA concentration. Additionally, 19 colorectal carcinoma patients after tumor removal were also recruited for plasma β-catenin mRNA measurement to further demonstrate the clinical usefulness of this test. Results: β-catenin mRNA was detected with median concentrations of 8737 (range: 1480-933,100), 1218 (range: 541-2,254) and 291 (range: 0-1,366) copies/mi plasma in colorectal carcinoma, colorectal adenoma, and apparently normal subjects, respectively. Statistical analysis demonstrated that plasma β-catenin mRNA concentration was correlated to tumor stage but not sex, age, lymph node status, and degree in differentiation. Moreover, plasma β-catenin mRNA concentration decreased significantly after tumor removal in 16 of 19 (84%) colorectal carcinoma patients. Conclusions: We conclude that plasma β-catenin mRNA may potentially serve as a marker for colorectal cancer.
UR - http://www.scopus.com/inward/record.url?scp=1842585925&partnerID=8YFLogxK
U2 - 10.1158/1078-0432.CCR-1168-3
DO - 10.1158/1078-0432.CCR-1168-3
M3 - Journal article
C2 - 15014011
SN - 1078-0432
VL - 10
SP - 1613
EP - 1617
JO - Clinical Cancer Research
JF - Clinical Cancer Research
IS - 5
ER -