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Peer-reviewed veterinary case report

Pevonedistat drug stops canine melanoma cell growth by causing DNA

By Wood, Elizabeth A et al.·Published in Veterinary and comparative oncology·2020·Department of Medical Sciences·View original on PubMed

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Original publication title: Pevonedistat targeted therapy inhibits canine melanoma cell growth through induction of DNA re-replication and senescence.

Species:
dog

Plain-English summary

A study found that a drug called pevonedistat (MLN4924) can significantly reduce the growth of melanoma cells in dogs, which is a type of skin cancer. When tested on canine melanoma cell lines and samples from dogs with the disease, the drug caused cancer cells to die and prevented them from growing. Most samples responded well to the treatment, although some were resistant. The researchers suggest that this drug could be a promising option for treating melanoma in dogs, but more studies are needed to confirm its effectiveness in clinical settings.

People also search for: dog melanoma treatment · pevonedistat for canine cancer · skin cancer in dogs · dog melanoma symptoms · canine melanoma survival rate

Abstract

MLN4924 (pevonedistat) is a potent and selective NEDD8-activating enzyme (NAE) inhibitor. The NEDD8-regulated neddylation system is responsible for the regulated degradation of intracellular proteins with important cellular functions in cancer cell growth, apoptosis, angiogenesis and metastasis. In human melanoma, inhibition of NAE results in induction of DNA re-replication, S phase cell cycle arrest, DNA damage and apoptosis. The study aimed to assess the anti-cancer effect of MLN4924 on canine malignant melanoma cell lines and patient samples and to elucidate the underlying mechanisms. Canine melanoma cell lines and primary patient samples were evaluated for cell viability after incubation with varying concentrations of MLN4924 or dimethyl sulfoxide. Apoptosis, cell proliferation and senescence assays were performed to address underlying mechanisms of MLN4924-mediated anti-tumour effects. Gene expression of seven previously identified deregulated genes in human melanoma was compared in sensitive vs resistant samples. MLN4924 treatment significantly reduced the viability of canine melanoma cell lines and primary samples in a dose- and time-dependent manners. MLN4924 promoted cell apoptosis and inhibited cell growth through induction of DNA re-replication and cell senescence. While the majority of canine melanoma samples demonstrated sensitivity at nanomolar ranges, some samples were resistant to the treatment. Modulation of P21 levels correlated with canine melanoma cell sensitivity. These results provided justification for further exploration of MLN4924 as a treatment of canine melanoma.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/31665821/