Novel Serum Biomarkers to Differentiate Cholangiocarcinoma from Benign Biliary Tract Diseases Using a Proteomic Approach

Disease Markers - Tập 2015 - Trang 1-11 - 2015
Tavan Janvilisri1, Kawin Leelawat2, Sittiruk Roytrakul3, Atchara Paemanee3, Rutaiwan Tohtong1
1Department of Biochemistry, Faculty of Science, Mahidol University, 272 Rama VI Road, Phayathai, Rajdhevi, Bangkok 10400, Thailand
2Department of Surgery, Rajavithi Hospital, Bangkok 10400, Thailand.
3Proteomics Research Laboratory, Genome Institute, National Center for Genetic Engineering and Biotechnology, NSTDA, Pathumthani 12120, Thailand.

Tóm tắt

Background and Aim. Cholangiocarcinoma (CCA) is the most frequent biliary malignancy, which poses high mortality rate due to lack of early detection. Hence, most CCA cases are present at the advanced to late stages with local or distant metastasis at the time of diagnosis. Currently available tumor markers including CA19-9 and CEA are inefficient and of limited usage due to low sensitivity and specificity. Here, we attempt to identify serum tumor markers for CCA that can effectively distinguish CCA from benign biliary tract diseases (BBTDs).Methods. Serum samples from 19 CCA patients and 17 BBTDs were separated by SDS-PAGE followed with LC-MS/MS and were subjected to statistical analysis and cross-validation to identify proteins whose abundance was significantly elevated or suppressed in CCA samples compared to BBTDs.Results. In addition to identifying several proteins previously known to be differentially expressed in CCA and BBTDs, we also discovered a number of molecules that were previously not associated with CCA. These included FAM19A5, MAGED4B, KIAA0321, RBAK, and UPF3B.Conclusions. Novel serum biomarkers to distinguish CCA from BBTDs were identified using a proteomic approach. Further validation of these proteins has the potential to provide a biomarker for differentiating CCA from BBTDs.

Từ khóa


Tài liệu tham khảo

10.1002/hep.22310

10.1055/s-2004-828889

10.1097/MOG.0b013e3282fbf9b3

10.1007/s00268-008-9778-3

2010, Hepatobiliary & Pancreatic Diseases International, 9, 219

10.1080/13651820801992716

10.1016/S0002-9270(99)00744-3

2004, World Journal of Gastroenterology, 10, 427, 10.3748/wjg.v10.i3.427

10.1007/s10620-005-2927-8

10.1007/s10620-008-0289-8

2003, Hepato-Gastroenterology, 50, 1259

10.1002/hep.1840100209

10.1016/S0002-9610(99)80090-7

2002, Hepato-Gastroenterology, 49, 616

10.1586/epr.09.8

10.1016/S0076-6879(06)11009-5

10.1038/nprot.2013.092

10.1093/nar/gks1094

10.1053/jhep.2002.32089

10.1002/cncr.27743

10.1016/j.canlet.2004.06.020

2006, World Journal of Gastroenterology, 12, 3740, 10.3748/wjg.v12.i23.3740

10.7314/APJCP.2013.14.1.557

1988, The Southeast Asian Journal of Tropical Medicine and Public Health, 19, 299

2003, Hepato-Gastroenterology, 50, 924

10.1177/1076029611427900

10.1016/j.ygeno.2003.10.006

10.1002/ijc.26200

10.1016/j.canlet.2012.03.025

10.1002/jso.23440

10.1016/j.bbalip.2006.03.011

10.1074/jbc.275.10.7212

10.1158/0008-5472.CAN-12-2130

10.1136/gutjnl-2011-301146