Literature DB >> 7284985

A deleted chromosome no. 13 in human retinoblastoma cells: relevance to tumorigenesis.

G Balaban-Malenbaum, F Gilbert, W W Nichols, R Hill, J Shields, A T Meadows.   

Abstract

In this report of banded karyotypes prepared after short-term culture (72 hr) from human retinoblastoma tumor tissue, on del(13)(pter leads to q14:) chromosome and one normal chromosome #13 were found in all of the metaphases examined. Similar deletions (always involving 13q14) have previously been described in the somatic cells of individuals with one form of retinoblastoma. In the present case, however, the constitutional karyotype is normal. The presence of tumors in both eyes suggests that this is the genetic form of retinoblastoma, even though the patient's family history is negative for this tumor. The normal constitutional karyotype argues that the chromosome deletion occurred as a postzygotic event. The modal chromosome number of the tumor cells is 47 and rearrangements involving chromosomes #2, #17, and #20 were also identified.

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Mesh:

Year:  1981        PMID: 7284985     DOI: 10.1016/0165-4608(81)90091-1

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


  9 in total

1.  Chromosomes of metastatic retinoblastoma.

Authors:  H A Daly; E V Davison; A D Pearson; M M Reid; A W Craft
Journal:  Arch Dis Child       Date:  1987-04       Impact factor: 3.791

2.  Isolation and regional localization of DNA segments revealing polymorphic loci from human chromosome 13.

Authors:  W Cavenee; R Leach; T Mohandas; P Pearson; R White
Journal:  Am J Hum Genet       Date:  1984-01       Impact factor: 11.025

3.  High rate of detection of 13q14 deletion mosaicism among retinoblastoma patients (using more extensive methods).

Authors:  T Motegi
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

4.  Chromosome 20 deletion in human multiple endocrine neoplasia types 2A and 2B: a double-blind study.

Authors:  V R Babu; D L Van Dyke; C E Jackson
Journal:  Proc Natl Acad Sci U S A       Date:  1984-04       Impact factor: 11.205

5.  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

6.  Similar chromosomal abnormalities in several retinoblastomas.

Authors:  L E Kusnetsova; E L Prigogina; H E Pogosianz; B M Belkina
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

7.  The association of a lymphoreticular malignancy with an 11q deletion: a coincidence or a cancer susceptibility?

Authors:  N L Rudd; I E Teshima
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

8.  Cause and consequences of genetic and epigenetic alterations in human cancer.

Authors:  B Sadikovic; K Al-Romaih; J A Squire; M Zielenska
Journal:  Curr Genomics       Date:  2008-09       Impact factor: 2.236

9.  Structural alterations of the RB1 gene in human soft tissue tumours.

Authors:  M R Stratton; S Williams; C Fisher; A Ball; G Westbury; B A Gusterson; C D Fletcher; J C Knight; Y K Fung; B R Reeves
Journal:  Br J Cancer       Date:  1989-08       Impact factor: 7.640

  9 in total

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