HMGIC expressed in a uterine leiomyoma with a deletion of the long arm of chromosome 7 along with a 12q14-15 rearrangement but not in tumors showing del(7) as the sole cytogenetic abnormality

被引:38
作者
Hennig, Y
Rogalla, P
Wanschura, S
Frey, G
Deichert, U
Bartnitzke, S
Bullerdiek, J
机构
[1] UNIV BREMEN,CTR HUMAN GENET & GENET COUNSELING,D-28359 BREMEN,GERMANY
[2] WOMENS CLIN,BREMEN,GERMANY
关键词
D O I
10.1016/S0165-4608(96)00283-X
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cytogenetic studies on uterine leiomyomas have shown that more than 60% of these tumors possess a normal karyotype and that 30% have clonal chromosomal aberrations. The most frequent changes are aberrations involving 12q14-15 and show rearrangements of the long arm of chromosome 7. Recently, we were able to demonstrate that in a variety of mesenchymal tumors showing 12q14-15 aberrations the HMGIC gene is rearranged thus playing a role in tumorigenesis. Here we report the results of HMGIC expression studies by RT-PCR of five uterine leiomyomas with different karyotypes. The RT-PCR studies were performed on two primary tumors showing a 12q14-15 aberration, one of which with an additional del(7) and three tumors with del(7) as the sole aberration. The tumor with the 12q14-15 aberration as the sole alteration and the leiomyoma with 12q14-15 rearrangement plus deletion of the long arm of chromosome 7 were shown to express HMGIC. In contrast, in all three tumors with the del(7) was the sole aberration no expression of HMGIC was noted. (C) Elsevier Science Inc., 1997.
引用
收藏
页码:129 / 133
页数:5
相关论文
共 21 条
[1]  
BERLINGIERI MT, 1995, MOL CELL BIOL, V15, P1545
[2]   AN INTERSTITIAL DELETION OF CHROMOSOME-7 MAY CHARACTERIZE A SUBGROUP OF UTERINE LEIOMYOMA [J].
BOGHOSIAN, L ;
DALCIN, P ;
SANDBERG, AA .
CANCER GENETICS AND CYTOGENETICS, 1988, 34 (02) :207-208
[3]   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
[4]   THE GENE FOR THE HUMAN ARCHITECTURAL TRANSCRIPTION FACTOR HMGI-C CONSISTS OF 5 EXONS EACH CODING FOR A DISTINCT FUNCTIONAL ELEMENT [J].
CHAU, KY ;
PATEL, UA ;
LEE, KLD ;
LAM, HYP ;
CRANEROBINSON, C .
NUCLEIC ACIDS RESEARCH, 1995, 23 (21) :4262-4266
[5]   CYTOGENETIC FINDINGS IN 9 LEIOMYOMAS OF THE UTERUS [J].
FAN, SX ;
SREEKANTAIAH, C ;
BERGER, CS ;
MEDCHILL, M ;
PEDRON, S ;
SANDBERG, AA .
CANCER GENETICS AND CYTOGENETICS, 1990, 47 (02) :179-189
[6]   COMPARISON OF MULTIPLE FORMS OF THE HIGH MOBILITY GROUP-I PROTEINS IN RODENT AND HUMAN-CELLS - IDENTIFICATION OF THE HUMAN HIGH MOBILITY GROUP-I-C PROTEIN [J].
GIANCOTTI, V ;
BANDIERA, A ;
BURATTI, E ;
FUSCO, A ;
MARZARI, R ;
COLES, B ;
GOODWIN, GH .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1991, 198 (01) :211-216
[7]   A SPECIFIC TRANSLOCATION, T(12,14)(Q14-15,Q23-24), CHARACTERIZES A SUBGROUP OF UTERINE LEIOMYOMAS [J].
HEIM, S ;
NILBERT, M ;
VANNI, R ;
FLODERUS, UM ;
MANDAHL, N ;
LIEDGREN, S ;
LECCA, U ;
MITELMAN, F .
CANCER GENETICS AND CYTOGENETICS, 1988, 32 (01) :13-17
[8]   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-&
[9]   DELETION OF BOTH CHROMOSOME-7 HOMOLOGS IN LEIOMYOMA [J].
KINGSLEY, KL ;
MELONI, AM ;
PEIER, AM ;
SANDBERG, AA ;
SURTI, U .
CANCER GENETICS AND CYTOGENETICS, 1995, 81 (01) :99-100
[10]  
MELONI AM, 1992, OBSTET GYNECOL, V80, P209