2008
DOI: 10.4161/cbt.7.8.6302
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Resveratrol displays converse dose-related effects on 5-fluorouracil-evoked colon cancer cell apoptosis: The roles of caspase-6 and p53

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Cited by 62 publications
(42 citation statements)
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References 19 publications
(28 reference statements)
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“…(40) In addition, our results show that Nr-CAM overexpression was associated with p53 expression, which is known to be associated with apoptotic resistance in colon cancer cells. (41) Indeed, it may be speculated that Nr-CAM overexpression confers resistance to 5-FU-evoked apoptosis in CRC cells. Nonetheless, as Nr-CAM overexpression is correlated with disease stage, it remains to be examined in larger studies if there exists a differential response to 5-FU-based chemotherapy at various stages of disease progression.…”
Section: Discussionmentioning
confidence: 99%
“…(40) In addition, our results show that Nr-CAM overexpression was associated with p53 expression, which is known to be associated with apoptotic resistance in colon cancer cells. (41) Indeed, it may be speculated that Nr-CAM overexpression confers resistance to 5-FU-evoked apoptosis in CRC cells. Nonetheless, as Nr-CAM overexpression is correlated with disease stage, it remains to be examined in larger studies if there exists a differential response to 5-FU-based chemotherapy at various stages of disease progression.…”
Section: Discussionmentioning
confidence: 99%
“…1,2 Resveratrol inhibits cancer cell growth in many cell lines, including cancers of the lung, prostate, colon, breast and ovaries. [3][4][5][6][7][8][9][10][11][12][13][14] Resveratrol also reduces tumor incidence in animal models by interfering with carcinogenesis through a wide array of anti-cancer actions. Several animal studies have demonstrated the ability of resveratrol to inhibit prostate cancer development by downregulating androgen receptors, inducing apoptosis/cell cycle arrest and inhibiting disease progression.…”
mentioning
confidence: 99%
“…The effect of resveratrol on fluorouracil-triggered apoptosis has been shown to hinge on the cellular p53 status (Chan et al 2008). Likewise, we have recently observed that the SIRT1/2 inhibitor tenovin-1 effectively killed p53 +/+ , but not p53 −/− cancer cells (Sonnemann et al 2014), further substantiating that the effects of sirtuin modulators can depend on p53.…”
Section: Single-agent Activity Of Resveratrol and Srt1720 Against Ewimentioning
confidence: 55%
“…These inconsistent findings might be due to diverse model systems, but they might as well be due to the use of different concentrations of resveratrol and/or divergent cellular p53 status. The latter consideration is supported by a publication which showed that resveratrol at lower concentrations antagonized the cytotoxic activity of fluorouracil in p53 +/+ , but not in p53 −/− colon cancer cells; in contrast, resveratrol amplified fluorouracil-mediated cell death at higher concentrations independent of p53 (Chan et al 2008).…”
Section: Introductionmentioning
confidence: 83%