Literature DB >> 3275489

Generation of homozygosity at the c-Ha-ras-1 locus on chromosome 11p in an adrenal adenoma from an adult with Wiedemann-Beckwith syndrome.

N K Hayward1, M H Little, R H Mortimer, W M Clouston, P J Smith.   

Abstract

Generation of homozygosity for the human c-Ha-ras-1 locus on the short arm of chromosome #11 (11p) has been demonstrated for an adrenal adenoma from an adult with Wiedemann-Beckwith syndrome (WBS). This is the first demonstration of loss of somatic heterozygosity for a locus on 11p in an adrenal neoplasm and is the first instance where a tumor of any type, from a patient with WBS, shows loss of heterozygosity in this region of the genome. Generation of homozygosity in an adenoma, rather than a carcinoma, demonstrates that this mechanism is an early event in tumorigenesis rather than a late event associated with tumor progression.

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Year:  1988        PMID: 3275489     DOI: 10.1016/0165-4608(88)90100-8

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


  5 in total

Review 1.  Discerning malignancy in resected adrenocortical neoplasms.

Authors:  H Sasano; T Suzuki; T Moriya
Journal:  Endocr Pathol       Date:  2001       Impact factor: 3.943

2.  Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.

Authors:  A Koufos; P Grundy; K Morgan; K A Aleck; T Hadro; B C Lampkin; A Kalbakji; W K Cavenee
Journal:  Am J Hum Genet       Date:  1989-05       Impact factor: 11.025

3.  Molecular definition of the 11p15.5 region involved in Beckwith-Wiedemann syndrome and probably in predisposition to adrenocortical carcinoma.

Authors:  I Henry; M Jeanpierre; P Couillin; F Barichard; J L Serre; H Journel; A Lamouroux; C Turleau; J de Grouchy; C Junien
Journal:  Hum Genet       Date:  1989-02       Impact factor: 4.132

4.  Loss of alleles on the short arm of chromosome 11 in a hepatoblastoma from a child with Beckwith-Wiedemann syndrome.

Authors:  M H Little; D B Thomson; N K Hayward; P J Smith
Journal:  Hum Genet       Date:  1988-06       Impact factor: 4.132

5.  Occasional loss of constitutive heterozygosity at 11p15.5 and imprinting relaxation of the IGFII maternal allele in hepatoblastoma.

Authors:  M Montagna; C Menin; L Chieco-Bianchi; E D'Andrea
Journal:  J Cancer Res Clin Oncol       Date:  1994       Impact factor: 4.553

  5 in total

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