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Effect of indirubin-3-monoxime against lung cancer as evaluated by histological and transmission electron microscopic studies.

Abstract
The aim of this study is to evaluate the antitumor effect of indirubin-3-monoxime and its mode of action in benzo(α)pyrene [B(α)P] induced lung cancer in A/J mice. Light microscopic examination of lung sections of [B(α)P] induced lung cancer mice revealed the presence of adenocarcinoma characterized by extensive proliferation of alveolar epithelium and loss of alveolar spaces. The control lung tissue showed a normal architecture with clear alveolar spaces. Interestingly the indirubin-3-monoxime treated groups showed the reduced adenocarcinoma with appearance of alveolar spaces. Transmission Electron Microscopic (TEM) studies of lung sections of [B(α)P] induced lung cancer mice showed the presence of phaemorphic cells with dense granules and increased mitochondria. The lung sections of mice treated with indirubin-3-monoxime showed the presence of shrunken, fragmented, and condensed nuclei implying apoptosis. The effects were dose dependent and prominent in 10 mg/kg/5 d/week groups suggesting the therapeutic role of indirubin analogue against this deadly human malignancy. Here, our results indicate that indirubin-3-monoxime brings antitumor effect against [B(α)P] induced lung cancer by its apoptotic action in A/J mice.
AuthorsKameswaran Ravichandran, Arttatrana Pal, Ramanibai Ravichandran
JournalMicroscopy research and technique (Microsc Res Tech) Vol. 73 Issue 11 Pg. 1053-8 (Oct 2010) ISSN: 1097-0029 [Electronic] United States
PMID20169620 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Copyright© 2010 Wiley-Liss, Inc.
Chemical References
  • Antineoplastic Agents
  • Indoles
  • Oximes
  • indirubin-3'-monoxime
  • Benzo(a)pyrene
Topics
  • Animals
  • Antineoplastic Agents (pharmacology)
  • Benzo(a)pyrene (toxicity)
  • Cell Count
  • Cell Nucleus (drug effects)
  • Cell Proliferation (drug effects)
  • Cell Shape (drug effects)
  • Cytoplasm (drug effects)
  • Histocytochemistry
  • Indoles (pharmacology)
  • Lung (anatomy & histology, cytology, pathology)
  • Lung Neoplasms (chemically induced, pathology)
  • Male
  • Mice
  • Microscopy, Electron, Transmission
  • Oximes (pharmacology)
  • Pulmonary Alveoli (cytology, drug effects)

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