Literature DB >> 6325938

Loss of a Harvey ras allele in sporadic Wilms' tumour.

A E Reeve, P J Housiaux, R J Gardner, W E Chewings, R M Grindley, L J Millow.   

Abstract

Genomic changes within chromosome band 11p13 appear to have a role in the initiation of Wilms' tumour. The human Harvey ras oncogene, c-Ha-ras 1, has been located by Jhanwar et al. immediately adjacent to this region at band 11p14 .1, although several groups have assigned the gene more distally at band 11p15 . We have examined tumour DNA from two cases of sporadic Wilms' tumour, and report here that in both cases one of the two constitutional c-Ha-ras 1 alleles was absent. One tumour had a reciprocal translocation between the short arm of chromosome 11 (at band 11p13), and the long arm of chromosome 12, with no visible loss of chromosomal material. The loss of a c-Ha-ras 1 allele in association with this translocation indicates that a submicroscopic deletion had occurred. The resulting hemizygosity may have had a role in tumour initiation. Our results indicate that the c-Ha-ras 1 gene and the 'Wilms' tumour locus' may be in close proximity. It would, therefore, be premature to exclude the possibility that these two sites are functionally related.

Entities:  

Mesh:

Substances:

Year:  1984        PMID: 6325938     DOI: 10.1038/309174a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  86 in total

Review 1.  renal tumors and tumor-like lesions in pediatric patients.

Authors:  J M Kissane; L P Dehner
Journal:  Pediatr Nephrol       Date:  1992-07       Impact factor: 3.714

2.  Oncogenic role of miR-483-3p at the IGF2/483 locus.

Authors:  Angelo Veronese; Laura Lupini; Jessica Consiglio; Rosa Visone; Manuela Ferracin; Francesca Fornari; Nicola Zanesi; Hansjuerg Alder; Gemma D'Elia; Laura Gramantieri; Luigi Bolondi; Giovanni Lanza; Patrizia Querzoli; Adriano Angioni; Carlo M Croce; Massimo Negrini
Journal:  Cancer Res       Date:  2010-04-13       Impact factor: 12.701

3.  Numerical aberrations of chromosomes 11 and 17 in colorectal adenocarcinomas.

Authors:  Y Tagawa; T Sawai; T Nakagoe; M Morinaga; T Yasutake; H Ayabe; M Tomita
Journal:  Surg Today       Date:  1996       Impact factor: 2.549

4.  Constitutional extra chromosomal element in a family with Wilms' tumor.

Authors:  S Kakati; H Xiao; S Y Siddiqui; C Sreekantaiah; H U Weier; D M Green; J E Fisher; J E Allen
Journal:  Hum Genet       Date:  1991-06       Impact factor: 4.132

5.  Cell culture studies on neurofibromatosis (von Recklinghausen). V. Monosomy 22 and other chromosomal anomalies in cultures from peripheral neurofibromas.

Authors:  W Krone; I Högemann
Journal:  Hum Genet       Date:  1986-12       Impact factor: 4.132

Review 6.  Tumor suppressor genes: a new era for molecular genetic studies of cancer.

Authors:  E Y Lee
Journal:  Breast Cancer Res Treat       Date:  1991-09       Impact factor: 4.872

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.  Measurements of the frequency of human erythrocytes with gene expression loss phenotypes at the glycophorin A locus.

Authors:  R G Langlois; W L Bigbee; R H Jensen
Journal:  Hum Genet       Date:  1986-12       Impact factor: 4.132

Review 9.  Genetic alterations in primary breast cancer.

Authors:  R Callahan
Journal:  Breast Cancer Res Treat       Date:  1989-07       Impact factor: 4.872

10.  Concordance between parental origin of chromosome 13q loss and chromosome 6p duplication in sporadic retinoblastoma.

Authors:  A Naumova; M Hansen; L Strong; P A Jones; D Hadjistilianou; D Mastrangelo; S Griegel; M F Rajewsky; J Shields; L Donoso
Journal:  Am J Hum Genet       Date:  1994-02       Impact factor: 11.025

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.