Specialized DNA arrays for the differentiation of pancreatic tumors

被引:34
作者
Buchholz, M
Kestler, HA
Bauer, A
Böck, W
Rau, B
Leder, G
Kratzer, W
Bommer, M
Scarpa, A
Schilling, MK
Adler, G
Hoheisel, JD
Gress, TM
机构
[1] Univ Ulm, Innere Med Abt 1, D-89081 Ulm, Germany
[2] Univ Ulm, Dept Visceral & Transplantat Surg, D-89081 Ulm, Germany
[3] Univ Ulm, Dept Internal Med 3, D-89081 Ulm, Germany
[4] Univ Ulm, Dept Neuroinformat, D-89081 Ulm, Germany
[5] Deutsch Krebsforschungszentrum, Div Funct Genome Anal, D-6900 Heidelberg, Germany
[6] Univ Saarland, Dept Gen Visceral & Vasc Surg, D-6650 Homburg, Germany
[7] Univ Verona, Dept Pathol, I-37100 Verona, Italy
关键词
D O I
10.1158/1078-0432.CCR-05-1274
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Malignant tumors of the pancreas are frequently indistinguishable from inflammatory tumors arising in the context of a chronic pancreatitis with the use of conventional imaging techniques. Thus, cytologic analysis of cells obtained by abdominal ultrasound, computed tomography, or endoscopic ultrasound-guided fine needle aspiration biopsy is required for diagnosis. However, the reliability of cytologic analyses of pancreatic fine needle aspirates remains unsatisfactory, with a diagnostic accuracy of <= 80%. The purpose of the current study was therefore to develop a novel diagnostic approach based on expression profiling of biopsy material using a specialized diagnostic c DNA array. Experimental Design: Previous gene expression profiling studies were reevaluated to design a 558-feature diagnostic array. Minimal amounts of residual material from pancreatic cytology samples as well as surgically resected tumor and control tissue specimens were analyzed using the diagnostic array and a newly developed statistical classification system. Results and Conclusions: Our diagnostic approach resulted in 95% accurate differentiation between ductal adenocarcinomas and nonmalignant tumors of the pancreas. The diagnostic array, in conjunction with conventional diagnostic procedures, is thus suitable to significantly improve the reliability of pancreatic cancer diagnostics and can be expected to become a valuable new tool in the routine workup of suspect masses in the pancreas.
引用
收藏
页码:8048 / 8054
页数:7
相关论文
共 32 条
[21]   Pancreatic cancer [J].
Li, DH ;
Xie, KP ;
Wolff, R ;
Abbruzzese, JL .
LANCET, 2004, 363 (9414) :1049-1057
[22]   p53 and K-ras mutations in pancreatic juice samples from patients with chronic pancreatitis [J].
Löhr, M ;
Müller, P ;
Mora, J ;
Brinkmann, B ;
Ostwald, C ;
Farré, A ;
Lluis, F ;
Adam, U ;
Stubbe, J ;
Plath, F ;
Nizze, H ;
Hopt, UT ;
Barten, M ;
Capellá, G ;
Liebe, S .
GASTROINTESTINAL ENDOSCOPY, 2001, 53 (07) :734-743
[23]  
Maitra A, 2003, CLIN CANCER RES, V9, P5988
[24]   Genome-wide cDNA microarray analysis of gene expression profiles in pancreatic cancers using populations of tumor cells and normal ductal epithelial cells selected for purity by laser microdissection [J].
Nakamura, T ;
Furukawa, Y ;
Nakagawa, H ;
Tsunoda, T ;
Ohigashi, H ;
Murata, K ;
Ishikawa, O ;
Ohgaki, K ;
Kashimura, N ;
Miyamoto, M ;
Hirano, S ;
Kondo, S ;
Katoh, H ;
Nakamura, Y ;
Katagiri, T .
ONCOGENE, 2004, 23 (13) :2385-2400
[25]   Ki-ras mutations and the carcinoembryonic antigen level in fine needle aspirates of the pancreas [J].
Pinto, MM ;
Emanuel, JR ;
Chaturvedi, V ;
Costa, J .
ACTA CYTOLOGICA, 1997, 41 (02) :427-434
[26]   Pancreatic intraductal sampling during ERCP in patients with chronic pancreatitis and pancreatic cancer:: cytologic studies and k-ras-2 codon 12 molecular analysis in 47 cases [J].
Pugliese, V ;
Pujic, N ;
Saccomanno, S ;
Gatteschi, B ;
Pera, C ;
Aste, H ;
Ferrara, GB ;
Nicolò, G .
GASTROINTESTINAL ENDOSCOPY, 2001, 54 (05) :595-599
[27]  
Swets John., 1982, EVALUATION DIAGNOSTI
[28]   Prospective evaluation of the contribution of K-ras mutational analysis and CA 19.9 measurement to cytological diagnosis in patients with clinical suspicion of pancreatic cancer [J].
Urgell, E ;
Puig, P ;
Boadas, J ;
Capellà, G ;
Queraltó, JM ;
Boluda, R ;
Antonijuan, A ;
Farré, A ;
Lluís, F ;
González-Sastre, F ;
Mora, J .
EUROPEAN JOURNAL OF CANCER, 2000, 36 (16) :2069-2075
[29]   Relative contribution of Ki-ras gene analysis and brush cytology during ERCP for the diagnosis of biliary and pancreatic diseases [J].
Van Laethem, JL ;
Bourgeois, V ;
Parma, J ;
Delhaye, M ;
Cochaux, P ;
Velu, T ;
Devière, J ;
Cremer, M .
GASTROINTESTINAL ENDOSCOPY, 1998, 47 (06) :479-485
[30]   Gene expression profiling predicts clinical outcome of breast cancer [J].
van't Veer, LJ ;
Dai, HY ;
van de Vijver, MJ ;
He, YDD ;
Hart, AAM ;
Mao, M ;
Peterse, HL ;
van der Kooy, K ;
Marton, MJ ;
Witteveen, AT ;
Schreiber, GJ ;
Kerkhoven, RM ;
Roberts, C ;
Linsley, PS ;
Bernards, R ;
Friend, SH .
NATURE, 2002, 415 (6871) :530-536