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Efficacy of polyphenon E, red ginseng, and rapamycin on benzo(a)pyrene-induced lung tumorigenesis in A/J mice.

Abstract
The objective of this investigation was to determine the efficacy of several novel agents in preventing lung tumorigenesis in mice. We evaluated polyphenon E, red ginseng, and rapamycin in A/J mice treated with the tobacco-specific carcinogen benzo(a)pyrene for their ability to inhibit pulmonary adenoma formation and growth. We found that treatment with polyphenon E exhibited a significant reduction on both tumor multiplicity and tumor load (tumor multiplicity x tumor volume) in a dose-dependent fashion. Polyphenon E (2% wt/wt) in the diet reduced tumor multiplicity by 46% and tumor load by 94%. This result provided key evidence in support of a phase II clinical chemoprevention trial of lung cancer. Administration of red ginseng in drinking water decreased tumor multiplicity by 36% and tumor load by 70%. The mammalian target of rapamycin inhibitor rapamycin showed significant efficacy against lung tumor growth in the tumor progression protocol and reduced tumor load by 84%. The results of these investigations demonstrate that polyphenon E, red ginseng, and rapamycin significantly inhibit pulmonary adenoma formation and growth in A/J mice.
AuthorsYing Yan, Yian Wang, Qing Tan, Yukihiko Hara, Taik-Koo Yun, Ronald A Lubet, Ming You
JournalNeoplasia (New York, N.Y.) (Neoplasia) Vol. 8 Issue 1 Pg. 52-8 (Jan 2006) ISSN: 1476-5586 [Electronic] United States
PMID16533426 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)
Chemical References
  • Antibiotics, Antineoplastic
  • Anticarcinogenic Agents
  • Antineoplastic Agents
  • Tea
  • Benzo(a)pyrene
  • Catechin
  • Protein Kinases
  • mTOR protein, mouse
  • TOR Serine-Threonine Kinases
  • polyphenon E
  • Sirolimus
Topics
  • Adenoma (pathology)
  • Animals
  • Antibiotics, Antineoplastic (pharmacology)
  • Anticarcinogenic Agents (pharmacology)
  • Antineoplastic Agents (pharmacology)
  • Benzo(a)pyrene (pharmacology)
  • Catechin (analogs & derivatives, pharmacology)
  • Female
  • Lung Neoplasms (chemically induced, drug therapy, pathology)
  • Mice
  • Panax (metabolism)
  • Protein Kinases (metabolism)
  • Sirolimus (pharmacology)
  • TOR Serine-Threonine Kinases
  • Tea

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