MicroRNA expression patterns to differentiate pancreatic adenocarcinoma from normal pancreas and chronic pancreatitis

被引:967
作者
Bloomston, Mark
Frankel, Wendy L.
Petrocca, Fabio
Volinia, Stefano
Alder, Hansjuerg
Hagan, John P.
Liu, Chang-Gong
Bhatt, Darshna
Taccioli, Cristian
Croce, Carlo M.
机构
[1] Ohio State Univ, James Canc Hosp, Div Surg Oncol, Columbus, OH 43210 USA
[2] Ohio State Univ, Solove Res Inst, Columbus, OH 43210 USA
[3] Ohio State Univ, Dept Mol Virol Immunol & Med Genet, Columbus, OH 43210 USA
[4] Ohio State Univ, Med Ctr, Dept Pathol, Columbus, OH 43210 USA
[5] Univ Ferrara, Dept Morphol & Embryol, I-44100 Ferrara, Italy
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2007年 / 297卷 / 17期
关键词
D O I
10.1001/jama.297.17.1901
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context While global microRNA ( miRNA) expression patterns of many embryologic, physiologic, and oncogenic processes have been described, description of the role of miRNAs in ductal adenocarcinoma of the pancreas is lacking. Objective To define the expression pattern of miRNAs in pancreatic cancer and compare it with those of normal pancreas and chronic pancreatitis. Design and Setting Specimens were obtained at a National Cancer Institute designated comprehensive cancer center from patients with ductal adenocarcinoma of the pancreas (n= 65) or chronic pancreatitis ( n= 42) ( January 2000-December 2005). All patients underwent curative pancreatectomy; those with pancreatic cancer were chemotherapy-naive. RNA harvested from resected pancreatic cancers and matched benign adjacent pancreatic tissue as well as from chronic pancreatitis specimens was hybridized to miRNA microarrays. Main Outcome Measures Identification of differentially expressed miRNAs that could differentiate pancreatic cancer from normal pancreas, chronic pancreatitis, or both, as well as a pattern of miRNA expression predictive of long-term ( > 24 months) survival. Significance of Analysis of Microarrays and Prediction of Analysis of Microarrays were undertaken to identify miRNAs predictive of tissue type and prognosis. P values were calculated by t test, adjusted for multiple testing. Kaplan-Meier survival curves were constructed using mean miRNA expression ( high vs low) as threshold and compared by log-rank analysis. Results Twenty-one miRNAs with increased expression and 4 with decreased expression were identified that correctly differentiated pancreatic cancer from benign pancreatic tissue in 90% of samples by cross validation. Fifteen overexpressed and 8 underexpressed miRNAs differentiated pancreatic cancer from chronic pancreatitis with 93% accuracy. A subgroup of 6 miRNAs was able to distinguish long-term survivors with node-positive disease from those dying within 24 months. Finally, high expression of miR-196a-2 was found to predict poor survival ( median, 14.3 months [95% confidence interval, 12.4-16.2] vs 26.5 months [ 95% confidence interval, 23.4-29.6]; P=. 009). Conclusions Pancreatic cancer may have a distinct miRNA expression pattern that may differentiate it from normal pancreas and chronic pancreatitis. miRNA expression patterns may be able to distinguish between long- and short-term survivors, but these findings need to be validated in other study populations.
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页码:1901 / 1908
页数:8
相关论文
共 28 条
[1]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[2]   Identification of molecular markers specific for pancreatic neuroendocrine tumors by genetic profiling of core biopsies [J].
Bloomston, M ;
Durkin, A ;
Yang, I ;
Rojiani, M ;
Rosemurgy, AS ;
Enkmann, S ;
Yeatman, TJ ;
Zervos, EE .
ANNALS OF SURGICAL ONCOLOGY, 2004, 11 (04) :413-419
[3]   A MicroRNA signature associated with prognosis and progression in chronic lymphocytic leukemia [J].
Calin, GA ;
Ferracin, M ;
Cimmino, A ;
Di Leva, G ;
Shimizu, M ;
Wojcik, SE ;
Iorio, MV ;
Visone, R ;
Sever, NI ;
Fabbri, M ;
Iuliano, R ;
Palumbo, T ;
Pichiorri, F ;
Roldo, C ;
Garzon, R ;
Sevignani, C ;
Rassenti, L ;
Alder, H ;
Volinia, S ;
Liu, CG ;
Kipps, TJ ;
Negrini, M ;
Croce, CM .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 353 (17) :1793-1801
[4]   MicroRNA-21 is an antiapoptotic factor in human glioblastoma cells [J].
Chan, JA ;
Krichevsky, AM ;
Kosik, KS .
CANCER RESEARCH, 2005, 65 (14) :6029-6033
[5]   Pre-B cell proliferation and lymphoblastic leukemia/high-grade lymphoma in Eμ-miR155 transgenic mice [J].
Costinean, S ;
Zanesi, N ;
Pekarsky, Y ;
Tili, E ;
Volinia, S ;
Heerema, N ;
Croce, CM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (18) :7024-7029
[6]   The genetics of pancreatic cancer [J].
Cowgill, SM ;
Muscarella, P .
AMERICAN JOURNAL OF SURGERY, 2003, 186 (03) :279-286
[7]  
De Lott LB, 2005, ARCH PATHOL LAB MED, V129, P1100
[8]   Oncomirs - microRNAs with a role in cancer [J].
Esquela-Kerscher, A ;
Slack, FJ .
NATURE REVIEWS CANCER, 2006, 6 (04) :259-269
[9]   Molecular prognostic markers in pancreatic cancer: A systematic review [J].
Garcea, G ;
Neal, CP ;
Pattenden, CJ ;
Steward, WP ;
Berry, DP .
EUROPEAN JOURNAL OF CANCER, 2005, 41 (15) :2213-2236
[10]   c-Fos expression as endogenous marker of lumbosacral spinal neuron activity in response to vaginocervical-stimulation [J].
Ghanima, A ;
Bennis, M ;
Rampin, O .
BRAIN RESEARCH PROTOCOLS, 2002, 9 (01) :1-8