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Dual Bioluminescence Imaging of Tumor Progression and Angiogenesis
Published on: August 1, 2019
Diosmetin inhibits tumor development and block tumor angiogenesis in skin cancer
Jawun Choi1, Dae-Hyo Lee1, Sang-Youel Park1
1College of Veterinary Medicine, Chonbuk National University, Iksan, Jeollabuk-do 54596, Republic of Korea.
Abstract:
Diosmetin is a natural flavonoid obtained from citrus fruits and some medicinal herbs. Previous studies have reported the anti-cancer activity of diosmetin in some types of tumors. However, it is still unclear whether diosmetin exerts anti-cancer effects, particularly anti-angiogenic effects, in skin cancer. In this study, we used B16F10 melanoma cells and human umbilical vein endothelial cells to investigate the inhibitory effect of diosmetin on cell proliferation, migration and tube formation in vitro. Rat aorta ring assays were performed to determine the effect of diosmetin on ECs sprouting ex vivo. Furthermore, a B16F10 mouse melanoma model was used to observe the effect of diosmetin on tumor growth, angiogenesis, and metastasis in vivo. Our results showed that diosmetin not only suppressed tumor cell proliferation and migration but also induced cell apoptosis via the caspase pathway in B16F10 cells, and potently inhibited tube formation and cell migration in HUVECs. Rat aorta ring assays showed that diosmetin attenuated the ECs sprouting. Moreover, the mouse melanoma model showed that diosmetin significantly delayed tumor growth by inhibiting tumor vessels sprouting and expansion during tumor progression. Notably, diosmetin induced the normalization of tumor vasculature through the downregulation of angiopoietin-2 and the improvement of pericyte coverage, leading to suppression of metastasis formation in lungs and lymph nodes. In conclusion, our results demonstrate that diosmetin suppresses tumor progression and metastasis by inducing tumor cell death and inhibiting tumor angiogenesis as well as normalizing the defective tumor vasculature, suggesting that diosmetin is a potential adjuvant chemotherapy agent.
Insights
Diosmetin, a natural flavonoid, inhibits skin cancer progression by reducing tumor cell growth, migration, and blood vessel formation. It also normalizes tumor vasculature, suppressing metastasis and suggesting potential as an adjuvant chemotherapy agent.
Area of Science:
- Oncology
- Pharmacology
- Biochemistry
Background:
- Diosmetin, a citrus flavonoid, shows anti-cancer potential in various tumors.
- Its anti-angiogenic effects in skin cancer remain largely unexplored.
- Understanding diosmetin's impact on melanoma is crucial for therapeutic development.
Purpose of the Study:
- To investigate the anti-cancer and anti-angiogenic effects of diosmetin on skin cancer.
- To evaluate diosmetin's efficacy in vitro, ex vivo, and in vivo using melanoma models.
- To explore diosmetin's mechanism of action on tumor cell proliferation, migration, apoptosis, and angiogenesis.
Main Methods:
- In vitro studies using B16F10 melanoma cells and human umbilical vein endothelial cells (HUVECs) assessed proliferation, migration, and tube formation.
- Ex vivo rat aorta ring assays evaluated endothelial cell (EC) sprouting.
- In vivo studies utilized a B16F10 mouse melanoma model to assess tumor growth, angiogenesis, and metastasis.
Main Results:
- Diosmetin suppressed melanoma cell proliferation, migration, and induced apoptosis via the caspase pathway.
- It potently inhibited HUVEC tube formation, migration, and EC sprouting in rat aorta rings.
- In vivo, diosmetin delayed tumor growth, inhibited tumor angiogenesis, normalized vasculature (downregulating angiopoietin-2, improving pericyte coverage), and reduced lung/lymph node metastasis.
Conclusions:
- Diosmetin exhibits significant anti-cancer and anti-angiogenic properties against skin cancer.
- It effectively suppresses tumor progression and metastasis by inducing apoptosis, inhibiting angiogenesis, and normalizing tumor vasculature.
- Diosmetin shows promise as a potential adjuvant chemotherapy agent for skin cancer treatment.
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