2015
DOI: 10.1016/j.bbrc.2015.03.141
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Stearidonic acid, a plant-based dietary fatty acid, enhances the chemosensitivity of canine lymphoid tumor cells

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Cited by 14 publications
(17 citation statements)
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“…Of particular note in relation to veterinary medicine and faty acids are two studies on canine tumor cell lines. The irst is that of canine lymphoma cell lines; in this study, stearidonic acid was shown to sensitize cells to anticancer drugs, even when the cells were previously resistant to drugs [84]. The second study utilized faty acids themselves as antitumor agents.…”
Section: Cancer Associations With Faty Acidsmentioning
confidence: 95%
“…Of particular note in relation to veterinary medicine and faty acids are two studies on canine tumor cell lines. The irst is that of canine lymphoma cell lines; in this study, stearidonic acid was shown to sensitize cells to anticancer drugs, even when the cells were previously resistant to drugs [84]. The second study utilized faty acids themselves as antitumor agents.…”
Section: Cancer Associations With Faty Acidsmentioning
confidence: 95%
“…Previous studies reported that the n-3 PUFA, such as DHA and SDA, were not cytotoxic at concentrations up to 200 μM in various cell culture systems [12,18]. In addition, it was reported that 400 μM of SDA was non-cytotoxic to healthy dog peripheral blood mononuclear cells [19]. Similar dietary fatty acids such as EPA and DHA in humans could attain up to 500 uM in plasma after oral intake in diet [20,21].…”
Section: Effects Of Sda On Cell Viability and Cytotoxicity In Lps-stimentioning
confidence: 98%
“…The measurements were performed in the presence or absence of a known ABCG2 inhibitor, nilotinib, or IND compounds. The ratio of intracellular Rh concentrations in the absence and presence of 5 μM nilotinib or IND compounds is indicative of the efflux activity of ABCG2 [17,23]. As shown in Fig.…”
Section: The Effect Of Ind Compounds and Nilotinib On The Intracellulmentioning
confidence: 99%
“…Rh (5 μM) was added to the cells in the presence or absence of nilotinib (positive control) or IND compounds and incubated for another 1 h. Subsequently, the medium was aspirated and the cells were washed with ice-cold PBS, trypsinized, washed three times with ice-cold PBS, and solubilized in 0.1% triton-PBS. To determine the intracellular concentration of Rh, the fluorescence was measured using Infinite microplate reader (Tecan Trading AG, Switzerland) at an excitation wavelength of 485 nm and an emission wavelength of 538 nm [17,23]. The ratio of intracellular Rh concentrations in the absence and presence of nilotinib or IND compounds will indicate the efflux activity of ABCG2.…”
Section: Intracellular Rhodamine 123 Accumulation Assaymentioning
confidence: 99%
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