Literature DB >> 3978590

Nonrandom chromosome alterations in rhabdomyosarcoma.

J Trent, J Casper, P Meltzer, F Thompson, J Fogh.   

Abstract

Chromosome banding analysis was attempted on tumor cells from a total of six rhabdomyosarcomas. Results revealed a variety of chromosome alterations, including frequent structural rearrangement of chromosome #1 and the finding in one patient of multiple double minutes. The single chromosome most consistently involved in structural rearrangements was #3. Simple deletion or translocation of either the long or short arm of chromosome #3 was found in all rhabdomyosarcoma tumors examined in this report. Further, a review of the limited previous literature on rhabdomyosarcoma provided further support for the frequent alteration of chromosome #3 in this disease. Results from our study provide preliminary evidence that alterations of chromosome 3p14-21 may represent a site of nonrandom chromosome change in rhabdomyosarcoma.

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Year:  1985        PMID: 3978590     DOI: 10.1016/0165-4608(85)90045-7

Source DB:  PubMed          Journal:  Cancer Genet Cytogenet        ISSN: 0165-4608


  16 in total

1.  Application of comparative genomic hybridization, spectral karyotyping, and microarray analysis in the identification of subtype-specific patterns of genomic changes in rhabdomyosarcoma.

Authors:  A Pandita; M Zielenska; P Thorner; J Bayani; R Godbout; M Greenberg; J A Squire
Journal:  Neoplasia       Date:  1999-08       Impact factor: 5.715

2.  A comparison of MyoD1 and fetal acetylcholine receptor expression in childhood tumors and normal tissues: implications for the molecular diagnosis of minimal disease in rhabdomyosarcomas.

Authors:  S Gattenloehner; B Dockhorn-Dworniczak; I Leuschner; A Vincent; H K Müller-Hermelink; A Marx
Journal:  J Mol Diagn       Date:  1999-11       Impact factor: 5.568

3.  A case of alveolar rhabdomyosarcoma with a chromosomal translocation, t(2;13)(q37;q14).

Authors:  T Nojima; S Abe; H Yamaguchi; T Matsuno; K Inoue
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1990

4.  The fetal form of the acetylcholine receptor distinguishes rhabdomyosarcomas from other childhood tumors.

Authors:  S Gattenloehner; A Vincent; I Leuschner; S Tzartos; H K Müller-Hermelink; T Kirchner; A Marx
Journal:  Am J Pathol       Date:  1998-02       Impact factor: 4.307

5.  Chromosome translocation (2;13)(q37;q14) in a disseminated alveolar rhabdomyosarcoma.

Authors:  R Engel; J Ritterbach; D Schwabe; F Lampert
Journal:  Eur J Pediatr       Date:  1988-10       Impact factor: 3.183

6.  Cytogenetic study of botryoid rhabdomyosarcoma of the uterine cervix.

Authors:  J P Palazzo; Z Gibas; C J Dunton; A Talerman
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1993

7.  Involvement of chromosome X in primary cytogenetic change in human neoplasia: nonrandom translocation in synovial sarcoma.

Authors:  C Turc-Carel; P Dal Cin; J Limon; U Rao; F P Li; J M Corson; R Zimmerman; D M Parry; J M Cowan; A A Sandberg
Journal:  Proc Natl Acad Sci U S A       Date:  1987-04       Impact factor: 11.205

8.  Pax3-FKHR knock-in mice show developmental aberrations but do not develop tumors.

Authors:  Irina Lagutina; Simon J Conway; Jack Sublett; Gerard C Grosveld
Journal:  Mol Cell Biol       Date:  2002-10       Impact factor: 4.272

9.  Cytogenetic investigations of solid tumours of children.

Authors:  A D Pearson; M M Reid; E V Davison; N Bown; A J Malcolm; A W Craft
Journal:  Arch Dis Child       Date:  1988-09       Impact factor: 3.791

10.  The most common fragile site in man is 3p14.

Authors:  D F Smeets; J M Scheres; T W Hustinx
Journal:  Hum Genet       Date:  1986-03       Impact factor: 4.132

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