CEACAM1, a novel serum biomarker for pancreatic cancer

被引:130
作者
Simeone, Diane M.
Ji, Baoan
Banerjee, Mousumi
Arumugam, Thiruvengadam
Li, Dawei
Anderson, Michelle A.
Bamberger, Ann Marie
Greenson, Joel
Brand, Randal E.
Ramachandran, ViJaya
Logsdon, Craig D.
机构
[1] Univ Michigan, Med Ctr, Dept Surg, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Mol & Integrat Physiol, Ann Arbor, MI 48109 USA
[3] Univ Texas, MD Anderson Canc Ctr, Dept Canc Biol, Houston, TX 77030 USA
[4] Univ Michigan, Dept Biostat, Ann Arbor, MI 48109 USA
[5] Univ Michigan, Dept Internal Med, Ann Arbor, MI 48109 USA
[6] Univ Hamburg, Dept Clin Chem, Hamburg, Germany
[7] Univ Michigan, Dept Pathol, Ann Arbor, MI 48109 USA
[8] Northwestern Healthcare, Evanston, IL USA
[9] Univ Texas, MD Anderson Canc Ctr, Dept Med Oncol, Houston, TX 77030 USA
关键词
pancreatic cancer; serum; biomarkers; CEACAM1; CA19-9; diagnosis;
D O I
10.1097/MPA.0b013e3180333ae3
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objectives: Serum biomarkers for early diagnosis of pancreatic adenocarcinoma are not currently available. We recently observed elevated expression of CEACAM1 in pancreatic adenocarcinomas and sought to determine whether serum CEACAM1 levels were elevated in pancreatic cancer patients. Methods: CEACAM1 messenger RNA levels were measured in pancreatic tissue samples using quantitative reverse transcription-polymerase chain reaction. CEACAM1 was localized by immunohistochemistry in adenocarcinomas and in pancreatic intraductal neoplasia lesions. CEACAM1 serum levels were assessed by a double determinant enzyme-linked immunosorbent assay and compared with serum levels of CA19-9. Results: CEACAM1 had higher expression levels in pancreatic adenocarcinomas compared with noncancerous pancreas (P < 0.0001) and was localized to neoplastic cells (95% (45/47) of adenocarcinomas and 85% (17/20) of pancreatic intraductal neoplasia 3 lesions. CEACAM1 was expressed in the sera of 91% (74/81) of pancreatic cancer patients, 24% (15/61) of normal patients, and 66% (35/53) of patients with chronic pancreatitis, with a sensitivity and specificity superior to CA19-9. The combination of CEACAM1 and CA19-9 had significantly higher diagnostic accuracy than CA19-9. Conclusions: CEACAM1 is expressed in pancreatic adenocarcinoma, and serum levels of CEACAM1 serve as a useful indicator for the presence of pancreatic cancer. Additional validation studies on the use of serum CEACAM1 as a diagnostic marker in pancreatic cancer are warranted.
引用
收藏
页码:436 / 443
页数:8
相关论文
共 38 条
[1]  
Bamberger AM, 1998, AM J PATHOL, V152, P1401
[2]   Diagnosis of pancreatic cancer using serum proteomic profiling [J].
Bhattacharyya, S ;
Siegel, ER ;
Petersen, GM ;
Chari, ST ;
Suva, LJ ;
Haun, RS .
NEOPLASIA, 2004, 6 (05) :674-686
[3]   cis interaction of the cell adhesion molecule CEACAM1 with integrin β3 [J].
Brümmer, J ;
Ebrahimnejad, A ;
Flayeh, R ;
Schumacher, U ;
Löning, T ;
Bamberger, AM ;
Wagener, C .
AMERICAN JOURNAL OF PATHOLOGY, 2001, 159 (02) :537-546
[4]   Loss of carcinoembryonic antigen-related cell adhesion molecule 1 expression is an adverse prognostic factor in hepatocellular carcinoma [J].
Cruz, PV ;
Wakai, T ;
Shirai, Y ;
Yokoyama, N ;
Hatakeyama, K .
CANCER, 2005, 104 (02) :354-360
[5]   AGA technical review on the epidemiology, diagnosis, and treatment of pancreatic ductal adenocarcinoma [J].
DiMagno, EP ;
Reber, HA ;
Tempero, MA .
GASTROENTEROLOGY, 1999, 117 (06) :1464-1484
[6]   IDENTIFICATION OF MEMBRANE-ANTIGENS IN GRANULOCYTES AND COLONIC-CARCINOMA CELLS BY A MONOCLONAL-ANTIBODY SPECIFIC FOR BILIARY GLYCOPROTEIN, A MEMBER OF THE CARCINOEMBRYONIC ANTIGEN FAMILY [J].
DRZENIEK, Z ;
LAMERZ, R ;
FENGER, U ;
WAGENER, C ;
HAUBECK, HD .
CANCER LETTERS, 1991, 56 (02) :173-179
[7]   CEA-related cell adhesion molecule 1:: A potent angiogenic factor and a major effector of vascular endothelial growth factor [J].
Ergün, S ;
Kilic, N ;
Ziegeler, G ;
Hansen, A ;
Nollau, P ;
Götze, J ;
Wurmbach, JH ;
Horst, A ;
Weil, J ;
Fernando, M ;
Wagener, C .
MOLECULAR CELL, 2000, 5 (02) :311-320
[8]   An autoantibody-mediated immune response to calreticulin isoforms in pancreatic cancer [J].
Hong, SH ;
Misek, DE ;
Wang, H ;
Puravs, E ;
Giordano, TJ ;
Greenson, JK ;
Brenner, DE ;
Simeone, DA ;
Logsdon, CD ;
Logsdon, D ;
Hanash, SM .
CANCER RESEARCH, 2004, 64 (15) :5504-5510
[9]   Pancreatic intraepithelial neoplasia -: A new nomenclature and classification system for pancreatic duct lesions [J].
Hruban, RH ;
Adsay, NV ;
Albores-Saavedra, J ;
Compton, C ;
Garrett, ES ;
Goodman, SN ;
Kern, SE ;
Klimstra, DS ;
Klöppel, G ;
Longnecker, DS ;
Lüttges, J ;
Offerhaus, GJA .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2001, 25 (05) :579-586
[10]  
HSIEH JT, 1995, CANCER RES, V55, P190