Literature DB >> 22870111

Possibility of using mRNA expression levels for nucleic acid-metabolizing enzymes within prostate cancer cells as indices for prognostic factors.

Akira Yano1, Yoshinori Shigematsu, Hiroyuki Kitano, Aki Hanayama, Akira Ozawa, Takatoshi Tacho, Motohiro Fujii.   

Abstract

Thymidylate synthase (TS), dihydropyrimidine dehydrogenase (DPD), thymidine phosphorylase (TP) and orotate phosphoribosyl transferase (OPRT) are enzymes involved in nucleic acid metabolism. It has been reported (based on observations of various tumor types) that the extent of the mRNA expression of these enzymes within tumor tissues may be used as a factor to define tumor prognosis. It has also been reported that the mRNA expression patterns differ in each type of tumor. However, few reports are available on the distribution of mRNA expression in prostate cancers. This study was conducted on tissue specimens obtained from 172 patients who were diagnosed with prostate cancer and had undergone total prostatectomies. The mRNA expression of TS, DPD, OPRT and TP was quantitatively analyzed using the Danenberg tumor profile (DTP) method. The results were used to examine the correlations between the distributions of the mRNAs and clinicopathological factors, as well as the significance of their expression as a prognostic factor. Patients with poorly differentiated cancers in their tissues showed a significant increase in the mRNA expression of TS and OPRT. The increases in the TP mRNA content were proportional to an increase in the Gleason scores. The prognosis was significantly poorer in those cases with a high expression of TS or OPRT mRNA and a low expression of DPD mRNA. In conclusion, the expression levels of mRNAs for TS, DPD and OPRT among the enzymes related to nucleic acid metabolism are useful as prognostic factors in patients with prostate cancers.

Entities:  

Year:  2010        PMID: 22870111      PMCID: PMC3412509          DOI: 10.3892/ol.2010.165

Source DB:  PubMed          Journal:  Oncol Lett        ISSN: 1792-1074            Impact factor:   2.967


  23 in total

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Journal:  Science       Date:  1996-11-08       Impact factor: 47.728

2.  Colorectal tumors responding to 5-fluorouracil have low gene expression levels of dihydropyrimidine dehydrogenase, thymidylate synthase, and thymidine phosphorylase.

Authors:  D Salonga; K D Danenberg; M Johnson; R Metzger; S Groshen; D D Tsao-Wei; H J Lenz; C G Leichman; L Leichman; R B Diasio; P V Danenberg
Journal:  Clin Cancer Res       Date:  2000-04       Impact factor: 12.531

3.  Prognostic predictors in breast cancer patients with postoperative 5-fluorouracil-based chemotherapy.

Authors:  Yasuhiko Hakamada; Akihiko Tsuchida; Masaaki Arima; Takeo Kubouchi; Hiromi Tokita; Daisuke Ota; Hiroshi Kaise; Toshiaki Aoki; Mikihiro Kusama; Tatsuya Aoki
Journal:  Int J Mol Med       Date:  2005-08       Impact factor: 4.101

4.  A comparison of 5-fluorouracil metabolism in human colorectal cancer and colon mucosa.

Authors:  G J Peters; C J van Groeningen; E J Laurensse; H M Pinedo
Journal:  Cancer       Date:  1991-11-01       Impact factor: 6.860

5.  High basal level gene expression of thymidine phosphorylase (platelet-derived endothelial cell growth factor) in colorectal tumors is associated with nonresponse to 5-fluorouracil.

Authors:  R Metzger; K Danenberg; C G Leichman; D Salonga; E L Schwartz; S Wadler; H J Lenz; S Groshen; L Leichman; P V Danenberg
Journal:  Clin Cancer Res       Date:  1998-10       Impact factor: 12.531

6.  Sensitivity of human, murine, and rat cells to 5-fluorouracil and 5'-deoxy-5-fluorouridine in relation to drug-metabolizing enzymes.

Authors:  G J Peters; E Laurensse; A Leyva; J Lankelma; H M Pinedo
Journal:  Cancer Res       Date:  1986-01       Impact factor: 12.701

7.  Clinical pharmacokinetics of 5-fluorouracil and its metabolites in plasma, urine, and bile.

Authors:  G D Heggie; J P Sommadossi; D S Cross; W J Huster; R B Diasio
Journal:  Cancer Res       Date:  1987-04-15       Impact factor: 12.701

8.  Predictive value of thymidylate synthase and dihydropyrimidine dehydrogenase expression in tumor tissue, regarding the efficacy of postoperatively administered UFT (tegafur+uracil) in patients with non-small cell lung cancer.

Authors:  Takanori Miyoshi; Kazuya Kondo; Hiroaki Toba; Mitsuteru Yoshida; Haruhiko Fujino; Koichiro Kenzaki; Shoji Sakiyama; Masatsugu Takehisa; Akira Tangoku
Journal:  Anticancer Res       Date:  2007 Jul-Aug       Impact factor: 2.480

9.  Thymidylate synthase, dihydropyrimidine dehydrogenase, orotate phosphoribosyltransferase mRNA and protein expression levels in solid tumors in large scale population analysis.

Authors:  Yousuke Fukui; Toshinori Oka; Sekio Nagayama; Peter V Danenberg; Kathleen D Danenberg; Masakazu Fukushima
Journal:  Int J Mol Med       Date:  2008-12       Impact factor: 4.101

10.  Both gene expression for orotate phosphoribosyltransferase and its ratio to dihydropyrimidine dehydrogenase influence outcome following fluoropyrimidine-based chemotherapy for metastatic colorectal cancer.

Authors:  W Ichikawa; H Uetake; Y Shirota; H Yamada; T Takahashi; Z Nihei; K Sugihara; Y Sasaki; R Hirayama
Journal:  Br J Cancer       Date:  2003-10-20       Impact factor: 7.640

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  1 in total

1.  Overexpression of thymidylate synthase (TYMS) is associated with aggressive tumor features and early PSA recurrence in prostate cancer.

Authors:  Christoph Burdelski; Christian Strauss; Maria Christina Tsourlakis; Martina Kluth; Claudia Hube-Magg; Nathaniel Melling; Patrick Lebok; Sarah Minner; Christina Koop; Markus Graefen; Hans Heinzer; Corinna Wittmer; Till Krech; Guido Sauter; Waldemar Wilczak; Ronald Simon; Thorsten Schlomm; Stefan Steurer
Journal:  Oncotarget       Date:  2015-04-10
  1 in total

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