Insulin-like growth factor-II gene expression in Wilms' tumour and embryonic tissues

• Published in: Nature (London) 1985-09, Vol.317 (6034), p.260-262
• Main Authors: Scott, J, Cowell, J, Robertson, M. E, Priestley, L. M, Wadey, R, Hopkins, B, Pritchard, J, Bell, G. I, Rall, L. B, Graham, C. F, Knott, T. J
• Format: Article
• Language: English
• Subjects: Biological and medical sciences; Female; Fetus - metabolism; Genes; Humanities and Social Sciences; Humans; Kidney - metabolism; Kidney Neoplasms - genetics; Kidneys; letter; Medical sciences; multidisciplinary; Neoplasms - genetics; Nephrology. Urinary tract diseases; Organ Specificity; Pregnancy; RNA, Messenger - genetics; RNA, Messenger - isolation & purification; Science; Science (multidisciplinary); Transcription, Genetic; Tumors of the urinary system; Wilms Tumor - genetics
• ISSN: 0028-0836; 1476-4687
• DOI: 10.1038/317260a0

Wilms' tumour (nephroblastoma) is an embryonal neoplasm occurring in hereditary and spontaneous forms. Both types show rearrangements of the short arm of chromosome 11. The germ line of children with the rare inherited triad of aniridia, genitourinary abnormality and mental retardation carry a chromosome 11 that has a deletion in its short arm (band 11p13) and these children are at increased risk of developing Wilms' tumour 1,2 . Neonates with the Beckwith–Wiedemann syndrome, in which there may be duplication of the 11p13–11p15 region, are similarly predisposed 3 . In the spontaneous form of the tumour a deletion of the Hp14 band in tumour cells, but not in normal cells, has been reported 4 , and the development of homozygosity for recessive mutations in the 11p region is implicated in the aetiology of Wilms' tumour 5–8 . In view of these chromosomal rearrangements and because Wilms' tumour is historically indistinguishable from the early stages of kidney development 9 , we have now examined the expression of genes localized to 11p in Wilms' tumour and human embryonic tissue. In 12 sporadic tumours examined, the expression of the gene coding for insulin-like growth factor-II (IGF-II), localized to the 11p15 region, was markedly increased relative to adult tissues, but was comparable to the level of expression in several fetal tissues including kidney, liver, adrenals and striated muscle. This may reflect the stage of tumour differentiation, but could also contribute to the malignant process, as IGF-II is an embryonal mitogen 10–13 .