2014
DOI: 10.1016/j.bbrc.2014.08.150
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Piceatannol promotes apoptosis via up-regulation of microRNA-129 expression in colorectal cancer cell lines

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Cited by 51 publications
(27 citation statements)
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“…Another study discovered the ability of piceatannol to depress colorectal cancer growth and clarified the participation of miR-129 in the anti-cancer action of piceatannol. The findings further suggested that piceatannol could be considered as a hopeful anticancer agent for CRC [70]. As mentioned previously, the miR-129-5p/HMGB1 axis could regulate irradiation-induced autophagy and might be a principal pathway in regulating radiosensitivity of breast cancer [72].…”
Section: Mir-129 As a Therapeutic Target For Human Cancersmentioning
confidence: 85%
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“…Another study discovered the ability of piceatannol to depress colorectal cancer growth and clarified the participation of miR-129 in the anti-cancer action of piceatannol. The findings further suggested that piceatannol could be considered as a hopeful anticancer agent for CRC [70]. As mentioned previously, the miR-129-5p/HMGB1 axis could regulate irradiation-induced autophagy and might be a principal pathway in regulating radiosensitivity of breast cancer [72].…”
Section: Mir-129 As a Therapeutic Target For Human Cancersmentioning
confidence: 85%
“…In colorectal cancer, Karaayvaz et al discovered a novel mechanism mediated by miR-129 to trigger apoptosis by suppressing a key antiapoptotic protein, B-cell lymphoma 2 (BCL2) [16], which was a central player in apoptosis of eukaryotic cells favoring survival by inhibiting cell death [69]. It was further found that piceatannol could stimulate the expression of miR-129, trigger down-regulation of Bcl-2, up-regulation of Bax and activation of caspase-3, and ultimately induce the apoptosis in CRC cells [70]. MiR-129-5p was also reported to inhibit the expression of VCP directly and play an important role in cell apoptosis of HCC [71].…”
Section: Mir-129 and Apoptosismentioning
confidence: 96%
“…In colorectal cancer cells, piceatannol treatment (30 μM) induced apoptosis by up-regulating miR-129, and thus down-regulating Bcl-2, which is a known target of miR-129 [186]. Besides, in prostate cancer cells, treatment with piceatannol (25 and 50 μM) inhibited proliferation, and induced cell cycle arrest and apoptosis, which might be associated with down-regulated mTOR [187].…”
Section: Experimental Studiesmentioning
confidence: 99%
“…A combination of resveratrol and quercetin decreased miR-27a level leading to an increasing expression of zinc finger protein repressor ZBTB10 known to suppress SP activity [511]. Piceatannol, a naturally occurring analog of resveratrol from roots of Picea abies , was shown to induce apoptosis in colorectal cancer cells (HCT116 and HT29) through upregulation of miR-129 levels, and downregulation of BCL2 level, as indicated in [512]. Knockdown of miR-129 counteracted the negative effect of piceatannol on viability of HCT116 and HT29 cells [512].…”
Section: Short Non-coding Micrornas and Natural Compoundsmentioning
confidence: 99%
“…Piceatannol, a naturally occurring analog of resveratrol from roots of Picea abies , was shown to induce apoptosis in colorectal cancer cells (HCT116 and HT29) through upregulation of miR-129 levels, and downregulation of BCL2 level, as indicated in [512]. Knockdown of miR-129 counteracted the negative effect of piceatannol on viability of HCT116 and HT29 cells [512]. Resveratrol, EGCG, and α-mangostin were shown to induce apoptosis and suppress the PI3K/AKT signaling pathway [513].…”
Section: Short Non-coding Micrornas and Natural Compoundsmentioning
confidence: 99%