TY - JOUR
T1 - Development of a multiplexed tumor-associated autoantibody-based blood test for the detection of colorectal cancer
AU - Fan, Chung Wei
AU - Kuo, Yung Bin
AU - Lin, Geng Pin
AU - Chen, Si Min
AU - Chang, Shih Hsien
AU - Li, Bo An
AU - Chan, Err Cheng
N1 - Publisher Copyright:
© 2017 Elsevier B.V.
PY - 2017/12
Y1 - 2017/12
N2 - Background Colorectal cancer (CRC) is one of the most common malignancies worldwide, and early diagnosis is vital to improving prognoses. We explored the diagnostic potential of a multiplex autoantibody panel as a biomarker for the detection of CRC by ELISA. Methods In total, 192 serum samples (92 CRC and 100 matched controls) were tested against a panel of 12 tumor-associated antigens (TAAs): RPH3AL, RPL36, SLP2, p53, survivin, ANAXA4, SEC61B, CCCAP, NYCO16, NMDAR, PLSCR1, and HDAC5. Individual and combined autoantibody signatures were examined. Results Compared to individual autoantibody markers, the combinations of TAAs provided better discrimination between tumorous and normal sera. The overall sensitivity of a selected panel of four antibodies (anti-SLP2, -p53, -SEC61B, and -PLSCR1) was 64.1%, with a specificity of 80% that increased to 83.7% when carcinoembryonic antigen (CEA) measurement was added. Furthermore, the sensitivity of the panel of four antibodies for early and advanced stages of CRC was 66.7% and 62%, increasing to 88.3% and 84%, respectively, when CEA was added. Conclusions We identified a panel of four antibodies as a promising diagnostic biomarker for the detection of CRC.
AB - Background Colorectal cancer (CRC) is one of the most common malignancies worldwide, and early diagnosis is vital to improving prognoses. We explored the diagnostic potential of a multiplex autoantibody panel as a biomarker for the detection of CRC by ELISA. Methods In total, 192 serum samples (92 CRC and 100 matched controls) were tested against a panel of 12 tumor-associated antigens (TAAs): RPH3AL, RPL36, SLP2, p53, survivin, ANAXA4, SEC61B, CCCAP, NYCO16, NMDAR, PLSCR1, and HDAC5. Individual and combined autoantibody signatures were examined. Results Compared to individual autoantibody markers, the combinations of TAAs provided better discrimination between tumorous and normal sera. The overall sensitivity of a selected panel of four antibodies (anti-SLP2, -p53, -SEC61B, and -PLSCR1) was 64.1%, with a specificity of 80% that increased to 83.7% when carcinoembryonic antigen (CEA) measurement was added. Furthermore, the sensitivity of the panel of four antibodies for early and advanced stages of CRC was 66.7% and 62%, increasing to 88.3% and 84%, respectively, when CEA was added. Conclusions We identified a panel of four antibodies as a promising diagnostic biomarker for the detection of CRC.
KW - Autoantibody
KW - Biomarker
KW - Colorectal cancer
UR - http://www.scopus.com/inward/record.url?scp=85032338246&partnerID=8YFLogxK
U2 - 10.1016/j.cca.2017.10.022
DO - 10.1016/j.cca.2017.10.022
M3 - 文章
C2 - 29074220
AN - SCOPUS:85032338246
SN - 0009-8981
VL - 475
SP - 157
EP - 163
JO - Clinica Chimica Acta
JF - Clinica Chimica Acta
ER -