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.
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Authors | Kameswaran Ravichandran, Arttatrana Pal, Ramanibai Ravichandran |
Journal | Microscopy research and technique
(Microsc Res Tech)
Vol. 73
Issue 11
Pg. 1053-8
(Oct 2010)
ISSN: 1097-0029 [Electronic] United States |
PMID | 20169620
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2010 Wiley-Liss, Inc. |
Chemical References |
- Antineoplastic Agents
- Indoles
- Oximes
- indirubin-3'-monoxime
- Benzo(a)pyrene
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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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