Literature DB >> 7530489

Trisomy 2, trisomy 20, and del(17p) as sole chromosomal abnormalities in three cases of hepatoblastoma.

V S Tonk1, K S Wilson, C F Timmons, N R Schneider.   

Abstract

Short-term cultures of three hepatoblastomas were analyzed cytogenetically. Trisomy 2, trisomy 20, and a deletion of 17p were found as the sole abnormalities, yielding the karyotypes 47,XY, + 2; 47,XX, + 20; and 46,XX,del(17)(p12)/46,XX. This is the first reported case of deletion of 17p as the sole chromosomal abnormality in a hepatoblastoma and the first reported case of trisomy 20 without double minute chromosomes as a sole chromosomal abnormality in hepatoblastoma.

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Year:  1994        PMID: 7530489     DOI: 10.1002/gcc.2870110309

Source DB:  PubMed          Journal:  Genes Chromosomes Cancer        ISSN: 1045-2257            Impact factor:   5.006


  3 in total

1.  Characterization of genomic alterations in hepatoblastomas. A role for gains on chromosomes 8q and 20 as predictors of poor outcome.

Authors:  R G Weber; T Pietsch; D von Schweinitz; P Lichter
Journal:  Am J Pathol       Date:  2000-08       Impact factor: 4.307

2.  Gene expression profiling reveals signatures characterizing histologic subtypes of hepatoblastoma and global deregulation in cell growth and survival pathways.

Authors:  Adekunle M Adesina; Dolores Lopez-Terrada; Kwong K Wong; Preethi Gunaratne; Yummy Nguyen; Joseph Pulliam; Judith Margolin; Milton J Finegold
Journal:  Hum Pathol       Date:  2009-02-05       Impact factor: 3.466

3.  Comparative genomic hybridization reveals population-based genetic alterations in hepatoblastomas.

Authors:  S G Gray; S Kytölä; T Matsunaga; C Larsson; T J Ekström
Journal:  Br J Cancer       Date:  2000-10       Impact factor: 7.640

  3 in total

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