Abstract | BACKGROUND:
Angiopoietin-2 (Ang-2) plays critical roles in vascular morphogenesis and its upregulation is frequently associated with various tumors. Previous studies showed that certain selenium compounds possess anti- tumor effects. However, the underlining mechanism has not been elucidated in detail. Plus, results of research on the anti- tumor effects of selenium compounds remain controversial. METHODS: RESULTS: Treatment of MDA-MB-231 cells with MSeA caused significant reduction of Ang-2 mRNA transcripts and secretion of Ang-2 proteins by the cells. Level of VEGF protein was accordingly decreased following the treatment. Compared with the controls, oral administration of MSeA (3 mg/kg/day for 18 days) to the nude mice carrying MDA-MB-231 induced tumors resulted in significant reduction in xenograft tumor volume and weights, significant decrease in microvascular density, and promotion of vascular normalization by increasing pericytes coverage. As expected, level of VEGF was also decreased in MSeA treated tumors. CONCLUSIONS: Our results point out that MSeA exerts its anti- tumor effects, at least in part, by inhibiting the Ang-2/Tie2 pathway, probably via inhibiting VEGF.
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Authors | Xiaojing Wu, Yidi Zhang, Zengyang Pei, Si Chen, Xu Yang, Yin Chen, Degui Lin, Runlin Z Ma |
Journal | BMC cancer
(BMC Cancer)
Vol. 12
Pg. 192
(May 28 2012)
ISSN: 1471-2407 [Electronic] England |
PMID | 22640261
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Angiopoietin-2
- Organoselenium Compounds
- Vascular Endothelial Growth Factor A
- methylselenic acid
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Topics |
- Angiopoietin-2
(antagonists & inhibitors, genetics, metabolism)
- Animals
- Blotting, Western
- Bone Neoplasms
(metabolism, prevention & control, secondary)
- Breast Neoplasms
(drug therapy, metabolism, pathology)
- Cell Line, Tumor
- Female
- Gene Expression
(drug effects)
- Humans
- Immunohistochemistry
- Mice
- Mice, Nude
- Organoselenium Compounds
(pharmacology)
- RNA Interference
- Reverse Transcriptase Polymerase Chain Reaction
- Signal Transduction
(drug effects, genetics)
- Tumor Burden
(drug effects)
- Vascular Endothelial Growth Factor A
(antagonists & inhibitors, genetics, metabolism)
- Xenograft Model Antitumor Assays
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