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January 1, 2014BioMed Research International260 citationsOpen Access

Sunitinib Combined with Angiotensin-2 Type-1 Receptor Antagonists Induces More Necrosis: A Murine Xenograft Model of Renal Cell Carcinoma

GVG. VerhoestTDThibault Dolley‐HitzeFJFlorence Jouan

Key Result

The combination of sunitinib and telmisartan significantly increased tissue necrosis (P=0.038) and decreased central microvascular density (P=0.0038) compared to sunitinib alone in a murine ccRCC model.

Structured PICO

Does the combination of sunitinib and telmisartan increase antiangiogenic effects and tumor necrosis in a murine xenograft model of renal cell carcinoma?

P
Population
40 nude mice with 786-O cell line-induced clear cell renal cell carcinoma xenografts, treated for four weeks.
I
Intervention
Sunitinib combined with telmisartan, administered orally daily for 4 weeks.
C
Comparator
Control (DMSO), sunitinib alone, and telmisartan alone.
O
Outcome
Tumor growth, tissue necrosis, central microvascular density, and circulating VEGF.surrogate

In a murine model of renal cell carcinoma, adding the angiotensin receptor blocker telmisartan to sunitinib enhanced antiangiogenic effects and increased tumor necrosis.

Main Result

p-value: p=0.038

Abstract

BACKGROUND: Angiotensin-2 type-1 receptor antagonists not are only antihypertensive drugs but also can inhibit VEGF production. We hypothesised that adding telmisartan to sunitinib could potentiate the antiangiogenic effects. MATERIAL AND METHODS: 786-O cell lines were injected in nude mice. After tumor development, mice were divided into 4 groups: the first was the control group (DMSO), the second group was treated with sunitinib alone, the third group was treated with telmisartan alone, and the fourth group was treated with the combination. Drugs were orally administered every day for four weeks. Animals were sacrificed after treatment. Blood and tumor tissues were collected for analysis by immunohistochemistry, Western Blot, and ELISA methods. RESULTS: All animals developed a ccRCC and ten in each group were treated. Using a kinetic model, tumors tended to grow slower in the combination group compared to others (P = 0.06). Compared to sunitinib alone, the addition of telmisartan significantly increased tissue necrosis (P = 0.038). Central microvascular density decreased (P = 0.0038) as well as circulating VEGF (P = 0.003). There was no significant variation in proliferation or apoptosis markers. CONCLUSION: The combination of sunitinib and telmisartan revealed an enhancement of the blockage of the VEGF pathway on renal tumor resulting in a decrease in neoangiogenesis and an increase in necrosis.

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Cite This Study

Verhoest et al. (2014) studied Renal Cell Carcinoma (murine xenograft model) (n=40). Sunitinib combined with telmisartan vs. Sunitinib alone, telmisartan alone, and control (DMSO) was evaluated on Tissue necrosis (p=0.038). The combination of sunitinib and telmisartan significantly increased tissue necrosis (P=0.038) and decreased central microvascular density (P=0.0038) compared to sunitinib alone in a murine ccRCC model.

synapsesocial.com/papers/6aa596d5bc2c7db7488e4463https://doi.org/10.1155/2014/901371
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