Literature DB >> 7116319

Abnormalities of chromosome #13 in retinoblastomas from individuals with normal constitutional karyotypes.

G Balaban, F Gilbert, W Nichols, A T Meadows, J Shields.   

Abstract

Constitutional chromosome abnormalities have been associated with retinoblastoma, Wilm's tumor, and a familial form of renal carcinoma. For each tumor type, the particular chromosome segment involved in the observed rearrangements is different: in retinoblastoma, that segment is band q14 on chromosome #13. We now present evidence that in retinoblastoma, structural abnormalities involving the particular chromosome segment identified in the constitutional cases can also occur in the tumors of individuals with normal constitutional karyotypes. Six cases with retinoblastoma in one or both eyes were analyzed; deletions/rearrangements involving 13q14 were found in the tumor cell karyotypes of five of the six. These observations suggest that changes in a gene or genes at a common site (13q14) play a role in tumorigenesis in all forms of retinoblastoma, sporadic as well as heritable.

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Year:  1982        PMID: 7116319     DOI: 10.1016/0165-4608(82)90058-9

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


  18 in total

1.  [Comparative genomic hybridization as cytogenetic tumor diagnosis technique in juvenile angiofibroma].

Authors:  H Löwenheim
Journal:  HNO       Date:  2003-12       Impact factor: 1.284

Review 2.  Role of the retinoblastoma gene in the initiation and progression of human cancer.

Authors:  W F Benedict; H J Xu; S X Hu; R Takahashi
Journal:  J Clin Invest       Date:  1990-04       Impact factor: 14.808

3.  Rhabdomyosarcoma-associated locus and MYOD1 are syntenic but separate loci on the short arm of human chromosome 11.

Authors:  H J Scrable; D K Johnson; E M Rinchik; W K Cavenee
Journal:  Proc Natl Acad Sci U S A       Date:  1990-03       Impact factor: 11.205

4.  Gene inactivation as a mechanism for the expression of recessive phenotypes.

Authors:  S G Grant; C E Campbell; C Duff; S L Toth; R G Worton
Journal:  Am J Hum Genet       Date:  1989-10       Impact factor: 11.025

5.  Radiographic findings in 13q-syndrome.

Authors:  S C Kaste; C B Pratt
Journal:  Pediatr Radiol       Date:  1993

6.  Loss of heterozygosity in human ductal breast tumors indicates a recessive mutation on chromosome 13.

Authors:  C Lundberg; L Skoog; W K Cavenee; M Nordenskjöld
Journal:  Proc Natl Acad Sci U S A       Date:  1987-04       Impact factor: 11.205

7.  Linkage analysis of a DNA marker localized to 20p12 and multiple endocrine neoplasia type 2A.

Authors:  P J Goodfellow; B N White; J J Holden; A M Duncan; E V Sears; H S Wang; L Berlin; K K Kidd; N E Simpson
Journal:  Am J Hum Genet       Date:  1985-09       Impact factor: 11.025

8.  A detailed analysis of chromosomal changes in heritable and non-heritable retinoblastoma.

Authors:  J Squire; B L Gallie; R A Phillips
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

Review 9.  Karyotypic progression in human tumors.

Authors:  S R Wolman
Journal:  Cancer Metastasis Rev       Date:  1983       Impact factor: 9.264

10.  Isochromosome 6p, a unique chromosomal abnormality in retinoblastoma: verification by standard staining techniques, new densitometric methods, and somatic cell hybridization.

Authors:  J Squire; R A Phillips; S Boyce; R Godbout; B Rogers; B L Gallie
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

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