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Peer-reviewed veterinary case report

Vegetable compound benzyl isothiocyanate kills canine lymphoma

By M. Henklewska et al.·Published in International Journal of Molecular Sciences·2021·View original on Semantic Scholar

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Original publication title: Benzyl Isothiocyanate, a Vegetable-Derived Compound, Induces Apoptosis via ROS Accumulation and DNA Damage in Canine Lymphoma and Leukemia Cells

Species:
dog

Plain-English summary

A study found that benzyl isothiocyanate (BITC), a compound from cruciferous vegetables, may help treat canine lymphoma and leukemia, which are common cancers in dogs. BITC was shown to kill cancer cells by causing them to undergo a process called apoptosis (cell death) and by generating oxidative stress. This means that BITC could be a promising natural treatment option for dogs with these types of cancer, especially those with B-cell neoplasms. While more research is needed, this study suggests that BITC could be a valuable addition to current chemotherapy treatments.

People also search for: dog lymphoma treatment · natural remedies for dog leukemia · BITC for canine cancer

Abstract

Treatment of neoplastic diseases in companion animals is one of the most important problems of modern veterinary medicine. Given the growing interest in substances of natural origin as potential anti-cancer drugs, our goal was to examine the effectiveness of benzyl isothiocyanate (BITC), a compound found in cruciferous vegetables, against canine lymphoma and leukemia. These are the one of the most common canine cancer types, and chemotherapy is the only treatment option. The study involved established cell lines originating from various hematopoietic malignancies: CLBL-1, GL-1, CLB70 and CNK-89, immortalized noncancerous cell lines: MDCK and NIH-3T3 and canine peripheral blood mononuclear cells (PBMCs). The cytotoxic activity of BITC, apoptosis induction, caspase activity and ROS generation were evaluated by flow cytometry. H2AX phosphorylation was assessed by western blot. The study showed that the compound was especially active against B lymphocyte-derived malignant cells. Their death resulted from caspase-dependent apoptosis. BITC induced ROS accumulation, and glutathione precursor N-acetyl-l-cysteine reversed the effect of the compound, thus proving the role of oxidative stress in BITC activity. In addition, exposure to the compound induced DNA damage in the tested cells. This is the first study that provides information on the activity of BITC in canine hematopoietic malignancies and suggests that the compound may be particularly useful in B-cell neoplasms treatment.

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Original publication on Semantic Scholar: https://www.semanticscholar.org/paper/34769202