Repuncturing the renal biopsy:: Strategies for molecular diagnosis in nephrology

被引:45
作者
Kretzler, M
Cohen, CD
Doran, P
Henger, A
Madden, S
Gröne, EF
Nelson, PJ
Schlöndorff, D
Gröne, HJ
机构
[1] Univ Munich, Med Poliklin, D-80336 Munich, Germany
[2] Univ Coll Dublin, Dept Med & Therapeut, Genom & Bioinformat Res Unit, Dublin 2, Ireland
[3] German Canc Res Ctr, Dept Cellular & Mol Pathol, Heidelberg, Germany
来源
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2002年 / 13卷 / 07期
关键词
D O I
10.1097/01.ASN.0000020390.29418.70
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
As has been exemplified by recent progress in the classification of cancer, future approaches to enhance the clinical diagnostic power of tissue biopsies may be based on gene expression profiles. A series of strategies to translate these approaches to the diagnosis of renal disease is here proposed. The theoretical and technical problems resulting from the small amount of starting material available from renal biopsies will be specifically addressed. A preliminary study with cDNA array-based expression data obtained from kidneys with tubulointerstitial inflammation and fibrosis suggests the feasibility of distinguishing molecular categories of renal disease. Finally, a combined conventional and molecular work-up of renal biopsies will be suggested. These approaches should add a new dimension to biopsy interpretation and provide novel information concerning renal pathogenesis, diagnosis, prognosis, and differential therapy. A coordinated effort from nephrologists and pathologists in large multicenter trials will be required to achieve this goal. It is hoped that this outlook will lead to stimulating discussions and the implementation of these innovative ideas in nephrology.
引用
收藏
页码:1961 / 1972
页数:12
相关论文
共 68 条
[11]   Cluster analysis and display of genome-wide expression patterns [J].
Eisen, MB ;
Spellman, PT ;
Brown, PO ;
Botstein, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (25) :14863-14868
[12]  
ERNST T, 2002, IN PRESS AM J PATHOL
[13]  
Esposito C, 1996, P ASSOC AM PHYSICIAN, V108, P209
[14]   Regulatory context is a crucial part of gene function [J].
Fessele, S ;
Maier, H ;
Zischek, C ;
Nelson, PJ ;
Werner, T .
TRENDS IN GENETICS, 2002, 18 (02) :60-63
[15]   Real-time quantitative RT-PCR after laser-assisted cell picking [J].
Fink, L ;
Seeger, W ;
Ermert, L ;
Hänze, J ;
Stahl, U ;
Grimminger, F ;
Kummer, W ;
Bohle, RM .
NATURE MEDICINE, 1998, 4 (11) :1329-1333
[16]   Preservation of RNA for functional genomic studies: A multidisciplinary tumor bank protocol [J].
Florell, SR ;
Coffin, CM ;
Holden, JA ;
Zimmermann, JW ;
Gerwels, JW ;
Summers, BK ;
Jones, DA ;
Leachman, SA .
MODERN PATHOLOGY, 2001, 14 (02) :116-128
[17]  
Frishberg Y, 2002, J AM SOC NEPHROL, V13, P400, DOI 10.1681/ASN.V132400
[18]   Immunomonitoring of renal transplant recipients in the early posttransplant period by analysis of cytokine gene expression in peripheral blood mononuclear cells [J].
Gibbs, PJ ;
Sadek, SA ;
Cameron, C ;
Tan, LC ;
Howell, WM .
TRANSPLANTATION PROCEEDINGS, 2001, 33 (7-8) :3285-3285
[19]   Molecular classification of cancer: Class discovery and class prediction by gene expression monitoring [J].
Golub, TR ;
Slonim, DK ;
Tamayo, P ;
Huard, C ;
Gaasenbeek, M ;
Mesirov, JP ;
Coller, H ;
Loh, ML ;
Downing, JR ;
Caligiuri, MA ;
Bloomfield, CD ;
Lander, ES .
SCIENCE, 1999, 286 (5439) :531-537
[20]  
Gröne HJ, 2002, J AM SOC NEPHROL, V13, DOI 10.1681/ASN.V134957