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Peer-reviewed veterinary case report

Soy isoflavones slow growth of canine lymphoma cells in lab tests

By Jamadar-Shroff, Vahbiz et al.·Published in Clinical cancer research : an official journal of the American Association for Cancer Research·2009·Department of Clinical Sciences, United States·View original on PubMed

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Original publication title: Soy-derived isoflavones inhibit the growth of canine lymphoid cell lines.

Species:
dog

Plain-English summary

A study looked at how a soy-based compound called genistein might help dogs with a type of cancer called B-cell lymphoma. While lab tests showed that genistein could kill cancer cells, when normal dogs were given the compound, their blood levels didn’t reach the amounts needed to be effective against the cancer. This means that while genistein shows promise in the lab, more research is needed to see if it can actually help dogs with lymphoma in real life.

People also search for: dog lymphoma treatment · genistein for dogs cancer · canine B-cell lymphoma options

Abstract

PURPOSE: This study aimed to evaluate the in vitro effects of genistein, both pure genistein and a commercially available form of genistein called Genistein Combined Polysacharride (GCP), against two canine B-cell lymphoid cell lines and determine the oral bioavailability of GCP when fed to normal dogs. EXPERIMENTAL DESIGN: The in vitro effect of genistein and GCP was evaluated using cell proliferation and apoptotic assays. The IC50 of both compounds was determined using a 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) cell proliferation assay and propidium idodide staining. Apoptosis was evaluated using Annexin V staining, caspase 3 and 9 staining, and DNA laddering. Cell cycle analysis and Bcl-2/Bax ratios were also examined. An initial dose escalating pharmacokinetic study was used to determine if therapeutic serum levels of genistein could be reached with oral dosing of GCP in normal dogs. RESULTS: The 72-hour in vitro IC50 of genistein and GCP against the GL-1 and 17-71 cells were both 10 microg/mL and 20 microg/mL, respectively. GCP led to cell death in both cell lines via apoptosis and treated cells exhibited increased Bax:Bcl-2 ratios. The serum concentrations of genistein in normal dogs given increasing oral doses of GCP did not reach the 72-hour in vitro IC50 in a dose escalation study. CONCLUSIONS: The results of these studies support the notion that canine high-grade B-cell lymphoma may represent a relevant large animal model of human non-Hodgkin's lymphoma to investigate the utility of GCP in chemopreventive and/or treatment strategies that may serve as a prelude to human clinical lymphoma trials.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/19228730/