Expression of the HMGA2-LPP fusion transcript in only 1 of 61 karyotypically normal pulmonary chondroid hamartomas

被引:5
作者
Lemke, I
Rogalla, P
Grundmann, F
Kunze, WP
Haupt, R
Bullerdiek, J [1 ]
机构
[1] Univ Bremen, Ctr Human Genet, D-2800 Bremen 33, Germany
[2] Practice Pathol, Hemer, Germany
[3] Urban Hosp St Georg, Inst Pathol, Leipzig, Germany
关键词
D O I
10.1016/S0165-4608(02)00595-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The HMGA2 gene has been found to be rearranged in a variety of benign solid tumors. However, in all tumor entities where aberrations of the corresponding chromosomal region have been found, a large percentage of tumors do not show any detectable cytogenetic deviation. Thus, the question arises whether or not in some of these cases, small subpopulations of tumor cells characterized by HMGA2 rearrangements exist. The existence of these populations would strongly suggest a secondary nature of the chromosomal aberrations. Herein, we have addressed this question by RT-PCR analyses of the HMGA2-LPP fusion resulting from t(3;12)(q27similar toq28;q14similar toq15) in a series of 61 pulmonary chondroid hamartomas (PCH) with an apparently normal karyotype. As a result, the HMGA2-LPP fusion transcript was amplified in only one of 61 PCH with a normal karyotype. In this case, fluorescence in situ hybridization analysis revealed a hidden chromosomal aberration. The absence of the HMGA2-LPP fusion in small populations of tumors with a normal karyotype suggests the primary nature of chromosomal rearrangements in the development of PCH affected by those aberrations. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:160 / 164
页数:5
相关论文
共 20 条
[1]  
ASHAR HR, 1995, CELL, V82, P57
[2]   REARRANGEMENTS OF CHROMOSOME REGION 12Q13-]Q15 IN PLEOMORPHIC ADENOMAS OF THE HUMAN SALIVARY-GLAND (PSA) [J].
BULLERDIEK, J ;
BARTNITZKE, S ;
WEINBERG, M ;
CHILLA, R ;
HAUBRICH, J ;
SCHLOOT, W .
CYTOGENETICS AND CELL GENETICS, 1987, 45 (3-4) :187-190
[3]  
Kazmierczak B, 1999, GENE CHROMOSOME CANC, V26, P125
[4]  
KAZMIERCZAK B, 1999, ELECT J PATHOLOGY, V5, P4
[5]   RAPID SUBCHROMOSOMAL LOCALIZATION OF COSMIDS BY NONRADIOACTIVE INSITU HYBRIDIZATION [J].
KIEVITS, T ;
DAUWERSE, JG ;
WIEGANT, J ;
DEVILEE, P ;
BREUNING, MH ;
CORNELISSE, CJ ;
VANOMMEN, GJB ;
PEARSON, PL .
CYTOGENETICS AND CELL GENETICS, 1990, 53 (2-3) :134-&
[6]   REGIONAL MAPPING OF THE HUMAN NSP GENE TO CHROMOSOME REGION 14Q21-]Q22 BY FLUORESCENCE IN-SITU HYBRIDIZATION ANALYSIS [J].
KOOLS, PFJ ;
ROEBROEK, AJM ;
VANDEVELDE, HJK ;
MARYNEN, P ;
BULLERDIEK, J ;
VANDEVEN, WJM .
CYTOGENETICS AND CELL GENETICS, 1994, 66 (01) :48-50
[7]   Large deletion of part of the HMGIC locus accompanying a t(3;12)(q27∼q28;q14∼q15) in a lipoma [J].
Lemke, I ;
Rogalla, P ;
Bullerdiek, J .
CANCER GENETICS AND CYTOGENETICS, 2001, 129 (02) :161-164
[8]   CHROMOSOMAL PATTERNS IN HUMAN BENIGN UTERINE LEIOMYOMAS [J].
MARK, J ;
HAVEL, G ;
GREPP, C ;
DAHLENFORS, R ;
WEDELL, B .
CANCER GENETICS AND CYTOGENETICS, 1990, 44 (01) :1-13
[9]   ANALYSIS OF ANDROGEN RECEPTOR DNA REVEALS THE INDEPENDENT CLONAL ORIGINS OF UTERINE LEIOMYOMATA AND THE SECONDARY NATURE OF CYTOGENETIC ABERRATIONS IN THE DEVELOPMENT OF LEIOMYOMATA [J].
MASHAL, RD ;
FEJZO, MLS ;
FRIEDMAN, AJ ;
MITCHNER, N ;
NOWAK, RA ;
REIN, MS ;
MORTON, CC ;
SKLAR, J .
GENES CHROMOSOMES & CANCER, 1994, 11 (01) :1-6
[10]  
Rogalla P, 1998, GENE CHROMOSOME CANC, V22, P100, DOI 10.1002/(SICI)1098-2264(199806)22:2<100::AID-GCC3>3.0.CO