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Differential effects of cryptoporic acids D and E, inhibitors of superoxide anion radical release, on tumor promotion of okadaic acid in mouse skin.

Abstract
Cryptoporic acids D and E, isolated from the fungus Cryptoporus volvatus, are inhibitors of superoxide anion radical release. Cryptoporic acid E inhibited tumor promotion of okadaic acid in two-stage carcinogenesis experiments on mouse skin, initiated with 7,12-dimethylbenz[a]anthracene. Treatment with cryptoporic acid E using two different doses per application, 1 (1.2 mumol) and 5 mg (5.9 mumol), reduced the percentage of tumor-bearing mice from 73.3 to 53.3% and 20.0%, and the average number of tumors per mouse from 4.2 to 2.3 and 0.5 respectively in week 20 of tumor promotion. However, cryptoporic acid D slightly enhanced tumor promotion rather than inhibition of okadaic acid. Cryptoporic acid D was expected to have additional biochemical activities, such as activation of protein kinases. Cryptoporic acid D at concentrations of up to 100 microM activated protein kinase C and stimulated other protein kinase activity in vitro, whereas cryptoporic acid E did not. These two compounds provided differential effects on tumor promotion of okadaic acid on mouse skin.
AuthorsS Matsunaga, H Furuya-Suguri, S Nishiwaki, S Yoshizawa, M Suganuma, T Hashimoto, Y Asakawa, H Fujiki
JournalCarcinogenesis (Carcinogenesis) Vol. 12 Issue 6 Pg. 1129-31 (Jun 1991) ISSN: 0143-3334 [Print] England
PMID1646082 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Carcinogens
  • Ethers, Cyclic
  • Free Radicals
  • Sesquiterpenes
  • Superoxides
  • cryptoporic acid D
  • cryptoporic acid E
  • Okadaic Acid
  • 9,10-Dimethyl-1,2-benzanthracene
  • Protein Kinases
  • Protein Kinase C
Topics
  • 9,10-Dimethyl-1,2-benzanthracene
  • Animals
  • Carcinogens
  • Enzyme Activation (drug effects)
  • Ethers, Cyclic (toxicity)
  • Female
  • Free Radicals
  • Mice
  • Okadaic Acid
  • Protein Kinase C (analysis)
  • Protein Kinases (analysis)
  • Sesquiterpenes (pharmacology)
  • Skin Neoplasms (chemically induced, prevention & control)
  • Superoxides (metabolism)

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