## Abstract ## BACKGROUND 2,3,7,8‐Tetrachlorodibenzo‐__p__‐dioxin (TCDD) exposure prior to chick embryo incubation (GD 0) induces dilated cardiomyopathy, and reduces myocardial hypoxia, vascular endothelial growth factor A (VEGF‐A) expression, and coronary vascularization. We investigated whether
Curcumin reduces pulmonary tumorigenesis in vascular endothelial growth factor (VEGF)-overexpressing transgenic mice
✍ Scribed by Yu-Tang Tung; Hsiao-Ling Chen; Cheng-Wei Lai; Chih-Jie Shen; Yi-Wen Lai; Chuan-Mu Chen
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 389 KB
- Volume
- 55
- Category
- Article
- ISSN
- 1613-4125
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Scope: We investigated the inhibition of pulmonary tumor formation through treatment with curcumin in transgenic mice.
Methods and results: In this study, a strain of transgenic mice carrying human vascular endothelial growth factor A~165~ (hVEGF‐A~165~) gene to induce pulmonary tumor was used as an in vivo cancer therapy model. We found that curcumin significantly reduced hVEGF‐A~165~ overexpression to normal, specifically in Clara cells of the lungs of transgenic mice, and suppressed the formation of tumors. In addition, we demonstrated a relationship between curcumin treatment and the expression of VEGF, EGFR, ERK2, and Cyclin A at the transcriptional and translational levels. We also noticed a reduction of Cyclin A and Cyclin B after curcumin treatment that had an effect on the cell cycle. Curcumin‐induced inhibition of Cyclin A and Cyclin B likely results in decreased progression through S and G2/M phases. These results demonstrated that the expression of proteins involved in the S to M phase transition in transgenic mice is suppressed by curcumin.
Conclusion: A Data suggest that a blockade of the cell cycle may be a critical mechanism for the observed effects on vasculogenesis and angiogenesis following treatment with curcumin.
📜 SIMILAR VOLUMES
## Abstract Her‐2/__neu__ (__erb__B‐2) oncogene overexpression is associated with increased tumor progression and metastasis. Fatty acid synthase (FAS), the key lipogenic enzyme responsible for the endogenous synthesis of fatty acids, has been shown to be one of the genes regulated by Her‐2/__neu__