Literature DB >> 1662795

A familial RB1 mutation detected by the HOT technique is homozygous in a second primary neoplasm.

E Weir-Thompson1, A Condie, R C Leonard, J Prosser.   

Abstract

Using the hydroxylamine-osmium tetroxide (HOT) technique, we have identified a constitutional point mutation in the retinoblastoma susceptibility gene (RB1) which segregates with the expression of retinoblastoma in five affected family members. One member developed a second primary tumor, a small-cell lung carcinoma (SCLC), which metastasized to the liver. Analysis of liver tumour DNA revealed homozygosity for the constitutional mutation, a G----A transition at the fifth base of intron 21, resulting in the excision of exon 21 from the mRNA. This is the first demonstration of homozygotization of a constitutional RB mutation in a metastatic second primary tumour and underlines the usefulness of the HOT technique for identification of mutations of the RB1 gene.

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Year:  1991        PMID: 1662795

Source DB:  PubMed          Journal:  Oncogene        ISSN: 0950-9232            Impact factor:   9.867


  11 in total

1.  The spectrum of RB1 germ-line mutations in hereditary retinoblastoma.

Authors:  D R Lohmann; B Brandt; W Höpping; E Passarge; B Horsthemke
Journal:  Am J Hum Genet       Date:  1996-05       Impact factor: 11.025

2.  Splicing aberrations caused by constitutional RB1 gene mutations in retinoblastoma.

Authors:  Vidya Latha Parsam; Mohammed Javed Ali; Santosh G Honavar; Geeta K Vemuganti; Chitra Kannabiran
Journal:  J Biosci       Date:  2011-06       Impact factor: 1.826

Review 3.  Putative non-Mendelian transmission of retinoblastoma in males: a phenotypic segregation analysis of 150 pedigrees.

Authors:  F L Munier; L Arabien; P Flodman; M A Spence; G Pescia; H P Rutz; A L Murphree
Journal:  Hum Genet       Date:  1994-11       Impact factor: 4.132

4.  The genetics of retinoblastoma, revisited.

Authors:  A Naumova; C Sapienza
Journal:  Am J Hum Genet       Date:  1994-02       Impact factor: 11.025

5.  Insertional inactivation of the WT1 gene in tumour cells from a patient with WAGR syndrome.

Authors:  A Santos; L Osorio-Almeida; P N Baird; J M Silva; M G Boavida; J Cowell
Journal:  Hum Genet       Date:  1993-08       Impact factor: 4.132

6.  Molecular mechanisms of oncogenic mutations in tumors from patients with bilateral and unilateral retinoblastoma.

Authors:  A Hogg; B Bia; Z Onadim; J K Cowell
Journal:  Proc Natl Acad Sci U S A       Date:  1993-08-01       Impact factor: 11.205

7.  RB1 gene mutation up-date, a meta-analysis based on 932 reported mutations available in a searchable database.

Authors:  José R Valverde; Javier Alonso; Itziar Palacios; Angel Pestaña
Journal:  BMC Genet       Date:  2005-11-04       Impact factor: 2.797

8.  Mechanisms of oncogenesis in patients with familial retinoblastoma.

Authors:  Z Onadim; A Hogg; J K Cowell
Journal:  Br J Cancer       Date:  1993-11       Impact factor: 7.640

9.  Characterization of keratin and cell cycle protein expression in cell lines from squamous intraepithelial lesions progressing towards a malignant phenotype.

Authors:  S Hietanen; K Syrjänen; S Syrjänen
Journal:  Br J Cancer       Date:  1998-03       Impact factor: 7.640

10.  The RB1 gene mutation in a child with ectopic intracranial retinoblastoma.

Authors:  Z Onadim; A J Woolford; J E Kingston; J L Hungerford
Journal:  Br J Cancer       Date:  1997       Impact factor: 7.640

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