Literature DB >> 7093963

Further evidence for the use of polyamines as biochemical markers for malignant tumors.

Y Horn, S L Beal, N Walach, W P Lubich, L Spigel, L J Marton.   

Abstract

One hundred ninety patients with a variety of tumor presented within a specified time period and fit a specified protocol. Multiple serial urinary putrescine, spermidine, and spermine levels were obtained in these patients, and their disease activity over time, defined as either active or nonactive, was determined by clinical examination, the results of laboratory tests, and radiological criteria. Twenty-four-hr urine collections were used for analysis of polyamine levels. A linear mixed-effects model and the method of maximum likelihood estimation were used for statistical analysis. Statistically significant differences were found in polyamine levels between patients with active or nonactive disease for tumors of the breast, stomach, prostate, female genital tract, and a variety of metastatic carcinomas of unknown origin. There were 105 patients with these tumors; 319 polyamine determinations were obtained from this subset of patients. Our results suggest that serial determination of polyamine levels in urine may have clinical utility for monitoring the disease states for these tumors.

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Year:  1982        PMID: 7093963

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  13 in total

1.  Polyamine metabolism in brain tumours: diagnostic relevance of quantitative biochemistry.

Authors:  R I Ernestus; G Röhn; R Schröder; T Els; W Paschen; N Klug
Journal:  J Neurol Neurosurg Psychiatry       Date:  2001-07       Impact factor: 10.154

2.  Mononuclear cell polyamine content associated with myeloid maturation in patients with leukemia during administration of polyamine inhibitors.

Authors:  A M Maddox; M J Keating; E J Freireich; M K Haddox
Journal:  Invest New Drugs       Date:  1989-07       Impact factor: 3.850

3.  ODC mRNA as a prognostic factor for predicting recurrence in meningiomas.

Authors:  A Klekner; A G Röhn; G Schillinger; R Schröder; N Klug; R I Ernestus
Journal:  J Neurooncol       Date:  2001-05       Impact factor: 4.130

4.  Polyamine metabolism in gliomas.

Authors:  R I Ernestus; G Röhn; R Schröder; T Els; J Y Lee; N Klug; W Paschen
Journal:  J Neurooncol       Date:  1996-08       Impact factor: 4.130

5.  Sequential inhibition of polyamine synthesis. A phase I trial of DFMO (alpha-difluoromethylornithine) and methyl-GAG [methylglyoxal-bis(guanylhydrazone)].

Authors:  R P Warrell; C J Coonley; J H Burchenal
Journal:  Cancer Chemother Pharmacol       Date:  1983       Impact factor: 3.333

6.  Alterations in human circulating and bone marrow mononuclear cell polyamine levels in hematologic malignancies as a consequence of difluoromethylornithine administration.

Authors:  A M Maddox; E J Freireich; M J Keating; K F Frasier-Scott; M K Haddox
Journal:  Invest New Drugs       Date:  1988-06       Impact factor: 3.850

7.  Tumour markers: An overview.

Authors:  T Malati
Journal:  Indian J Clin Biochem       Date:  2007-09

8.  Evaluation of polyamine levels in cerebrospinal fluid of children with brain tumors.

Authors:  Y Takaue; K Nishioka; J van Eys
Journal:  J Neurooncol       Date:  1986       Impact factor: 4.130

9.  Phase I evaluation of intravenous difluoromethylornithine--a polyamine inhibitor.

Authors:  A M Maddox; M J Keating; K E McCredie; E Estey; E J Freireich
Journal:  Invest New Drugs       Date:  1985       Impact factor: 3.850

10.  Urinary N1-acetylspermidine and N8-acetylspermidine excretion in normal humans and in patients with colorectal cancer.

Authors:  B L O'Brien; M Hankewych; D McCormick; R Jacoby; T A Brasitus; A G Halline
Journal:  Dig Dis Sci       Date:  1995-06       Impact factor: 3.199

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