Renin gene expression in nephroblastoma. 1990

G B Lindop, and K Duncan, and D W Millan, and A A Gibson, and W J Patrick, and B J Leckie, and G D Birnie
University of Glasgow, Department of Pathology, Western Infirmary.

Most cases of nephroblastoma have high plasma levels of prorenin which is biologically inactive. Plasma prorenin levels fall to normal following nephrectomy. In order to ascertain whether renin synthesis occurs in nephroblastomas we decided to search for renin-specific mRNA using a cDNA probe and Northern blot analyses on total RNA purified from snap-frozen human tumour tissue obtained at nephrectomy. We demonstrated renin-specific mRNA in 5/11 (45 per cent) nephroblastomas. It was 1.6 Kb in length, similar to the mRNA detected in normal kidney tissue and in kidneys with renal artery stenosis. In one of the cases of nephroblastoma, in which we could detect no normal renin mRNA at 1.6 Kb, the cDNA probe hybridized with a higher molecular weight mRNA 3 Kb in length. We conclude that some nephroblastomas synthesize renin.

UI MeSH Term Description Entries
D007680 Kidney Neoplasms Tumors or cancers of the KIDNEY. Cancer of Kidney,Kidney Cancer,Renal Cancer,Cancer of the Kidney,Neoplasms, Kidney,Renal Neoplasms,Cancer, Kidney,Cancer, Renal,Cancers, Kidney,Cancers, Renal,Kidney Cancers,Kidney Neoplasm,Neoplasm, Kidney,Neoplasm, Renal,Neoplasms, Renal,Renal Cancers,Renal Neoplasm
D009396 Wilms Tumor A malignant kidney tumor, caused by the uncontrolled multiplication of renal stem (blastemal), stromal (STROMAL CELLS), and epithelial (EPITHELIAL CELLS) elements. However, not all three are present in every case. Several genes or chromosomal areas have been associated with Wilms tumor which is usually found in childhood as a firm lump in a child's side or ABDOMEN. Bilateral Wilms Tumor,Nephroblastoma,Wilms Tumor 1,Wilms' Tumor,Nephroblastomas,Tumor, Bilateral Wilms,Tumor, Wilms,Tumor, Wilms',Wilm Tumor,Wilm's Tumor,Wilms Tumor, Bilateral
D012083 Renin A highly specific (Leu-Leu) endopeptidase that generates ANGIOTENSIN I from its precursor ANGIOTENSINOGEN, leading to a cascade of reactions which elevate BLOOD PRESSURE and increase sodium retention by the kidney in the RENIN-ANGIOTENSIN SYSTEM. The enzyme was formerly listed as EC 3.4.99.19. Angiotensin-Forming Enzyme,Angiotensinogenase,Big Renin,Cryorenin,Inactive Renin,Pre-Prorenin,Preprorenin,Prorenin,Angiotensin Forming Enzyme,Pre Prorenin,Renin, Big,Renin, Inactive
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D012333 RNA, Messenger RNA sequences that serve as templates for protein synthesis. Bacterial mRNAs are generally primary transcripts in that they do not require post-transcriptional processing. Eukaryotic mRNA is synthesized in the nucleus and must be exported to the cytoplasm for translation. Most eukaryotic mRNAs have a sequence of polyadenylic acid at the 3' end, referred to as the poly(A) tail. The function of this tail is not known for certain, but it may play a role in the export of mature mRNA from the nucleus as well as in helping stabilize some mRNA molecules by retarding their degradation in the cytoplasm. Messenger RNA,Messenger RNA, Polyadenylated,Poly(A) Tail,Poly(A)+ RNA,Poly(A)+ mRNA,RNA, Messenger, Polyadenylated,RNA, Polyadenylated,mRNA,mRNA, Non-Polyadenylated,mRNA, Polyadenylated,Non-Polyadenylated mRNA,Poly(A) RNA,Polyadenylated mRNA,Non Polyadenylated mRNA,Polyadenylated Messenger RNA,Polyadenylated RNA,RNA, Polyadenylated Messenger,mRNA, Non Polyadenylated
D015870 Gene Expression The phenotypic manifestation of a gene or genes by the processes of GENETIC TRANSCRIPTION and GENETIC TRANSLATION. Expression, Gene,Expressions, Gene,Gene Expressions

Related Publications

G B Lindop, and K Duncan, and D W Millan, and A A Gibson, and W J Patrick, and B J Leckie, and G D Birnie
September 1996, The Journal of pathology,
G B Lindop, and K Duncan, and D W Millan, and A A Gibson, and W J Patrick, and B J Leckie, and G D Birnie
July 1984, Journal of clinical pathology,
G B Lindop, and K Duncan, and D W Millan, and A A Gibson, and W J Patrick, and B J Leckie, and G D Birnie
May 1991, Journal of pediatric surgery,
G B Lindop, and K Duncan, and D W Millan, and A A Gibson, and W J Patrick, and B J Leckie, and G D Birnie
March 1987, Journal of pediatric surgery,
G B Lindop, and K Duncan, and D W Millan, and A A Gibson, and W J Patrick, and B J Leckie, and G D Birnie
February 1990, American journal of hypertension,
G B Lindop, and K Duncan, and D W Millan, and A A Gibson, and W J Patrick, and B J Leckie, and G D Birnie
August 1992, British journal of anaesthesia,
G B Lindop, and K Duncan, and D W Millan, and A A Gibson, and W J Patrick, and B J Leckie, and G D Birnie
April 1991, Archives of disease in childhood,
G B Lindop, and K Duncan, and D W Millan, and A A Gibson, and W J Patrick, and B J Leckie, and G D Birnie
June 1970, Archives of disease in childhood,
G B Lindop, and K Duncan, and D W Millan, and A A Gibson, and W J Patrick, and B J Leckie, and G D Birnie
October 2004, Biochemical pharmacology,
G B Lindop, and K Duncan, and D W Millan, and A A Gibson, and W J Patrick, and B J Leckie, and G D Birnie
September 1991, Clinical science (London, England : 1979),
Copied contents to your clipboard!