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The QM gene is X-linked and therefore not involved in suppression of tumorigenesis in Wilms' tumor

โœ Scribed by Ans M. W. Ouweland; Marian Verdijk; Marcel M. A. M. Mannens; Bernard A. Oost


Book ID
104666252
Publisher
Springer
Year
1992
Tongue
English
Weight
349 KB
Volume
90
Category
Article
ISSN
0340-6717

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โœฆ Synopsis


Inactivation of one or more tumor-suppressor genes on the short arm of chromosome 11 is thought to play a role in the etiology of Wilms' tumor. A candidate gene, QM, was recently isolated by subtractive hybridization between a tumorigenic cell line (deleted for part of 11p) and a non-tumorigenic cell line (the tumorigenic cell line carrying an extra t(X;11)copy). We show here with an exon-specific polymerase chain reaction that the genomic homolog of the QM cDNA is located in the G6PD-color vision genes region in Xq28. No homologous sequences could be detected on 11p. Our experiments indicate that the QM gene is not involved in the suppression of Wilms' tumor.


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The Simpson-Golabi-Behmel gene,GPC3, is
โœ Gillan, Tanya L. ;Hughes, Rhiannon ;Godbout, Roseline ;Grundy, Paul E. ๐Ÿ“‚ Article ๐Ÿ“… 2003 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 126 KB ๐Ÿ‘ 2 views

## Abstract Many genes have been implicated in Wilms tumor; however, only one gene, __WT1__, has a proven role in the development of this embryonal tumor. Wilms tumor occurs in a number of congenital syndromes including the Simpsonโ€“Golabiโ€“Behmel syndrome (SGBS) which has phenotypic overlap with ano