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Modeling Spontaneous Metastatic Renal Cell Carcinoma (mRCC) in Mice Following Nephrectomy
Published on: April 29, 2014
AE-941, a multifunctional antiangiogenic compound: trials in renal cell carcinoma
1Experimental Therapeutics Program, The Cleveland Clinic Taussig Cancer Center, Cleveland, OH 44195, USA. bukowsr@cc.ccf.org
Abstract:
The therapy of renal cell carcinoma remains a challenge for medical oncologists and urologists. During the past 10 years, the molecular abnormalities occurring in various subtypes of renal cancer, such as clear cell renal carcinoma, have been well described. The genetic abnormalities found in clear cell tumours involve chromosome 3p and, additionally, hypermethylation of the von Hippel-Lindau (VHL) gene can be detected. The VHL protein is involved in the angiogenic cascade in non-hypoxic conditions, and the possible role of mutant or hypermethylated VHL protein in promoting angiogenesis is, therefore, of interest. The majority of patients with renal cell carcinoma who receive treatment, such as IL-2 and/or IFN, fail and develop progressive disease. Therapy is therefore inadequate and novel approaches, such as those inhibiting angiogenesis, are of interest. The agent AE-941 (Neovostat trade mark; AEterna) was developed based on the observation that shark cartilage may contain biologically active inhibitors of angiogenesis. A variety of in vitro and in vivo activities of this preparation have been identified. At the molecular level, AE-941 appears to exhibit four different potential mechanisms of action: modulation of matrix proteases; inhibition of vascular endothelial growth factor binding to its receptor; induction of endothelial cell apoptosis; and stimulation of angiostatin production. The antitumour effects of AE-941 are seen in multiple murine models and involve not only effects on primary tumour growth but also on development of metastases. AE-941 is administered orally and has an excellent toxicity profile. Of interest are the findings in patients with renal cell carcinoma. Preliminary trials in this setting have suggested that responses to AE-941 occur and that patients receiving higher doses of this agent may have improved survival. Based on these preliminary data, a large, multi-institutional, randomised, Phase III trial of this agent has now been conducted in patients with metastatic clear cell carcinoma of the kidney. Over 300 patients have been entered into this trial, accrual is complete and results still remain preliminary. The clinical studies in a malignancy such as renal cell carcinoma will provide sentinel and potentially important observations on the clinical effectiveness of this agent.
Insights
AE-941, derived from shark cartilage, shows promise in treating renal cell carcinoma by inhibiting angiogenesis. Early trials suggest improved survival, leading to a large Phase III study in metastatic clear cell kidney cancer.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Renal cell carcinoma (RCC) therapy is challenging, with limited success for current treatments like IL-2 and IFN.
- Molecular abnormalities in clear cell RCC, including chromosome 3p alterations and von Hippel-Lindau (VHL) gene hypermethylation, are linked to tumor angiogenesis.
- The VHL protein's role in angiogenesis suggests that targeting this pathway could be a novel therapeutic strategy for RCC.
Purpose of the Study:
- To evaluate the efficacy and safety of AE-941 (Neovostat), an angiogenesis inhibitor derived from shark cartilage, in patients with metastatic clear cell renal cell carcinoma.
- To explore the potential of AE-941 as a novel therapeutic agent for RCC, addressing the unmet need for more effective treatments.
Main Methods:
- AE-941's in vitro and in vivo activities were identified, including modulation of matrix proteases, inhibition of vascular endothelial growth factor (VEGF) binding, induction of endothelial cell apoptosis, and stimulation of angiostatin production.
- Preclinical studies in murine models demonstrated AE-941's antitumour effects on primary tumors and metastases.
- A large, multi-institutional, randomized Phase III trial was conducted in over 300 patients with metastatic clear cell RCC, with AE-941 administered orally.
Main Results:
- Preliminary trials in RCC patients indicated responses to AE-941, with higher doses potentially correlating with improved survival.
- Preclinical studies showed AE-941's effectiveness against primary tumors and metastases in various murine models.
- AE-941 demonstrated an excellent toxicity profile in oral administration.
Conclusions:
- AE-941 exhibits multiple mechanisms of action that inhibit angiogenesis and possess antitumour activity.
- Preliminary clinical data suggest AE-941 may offer a survival benefit in patients with metastatic clear cell RCC.
- The ongoing Phase III trial is expected to provide definitive data on the clinical effectiveness of AE-941 for this challenging malignancy.
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