2015
DOI: 10.1016/j.canlet.2014.11.017
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Piperine inhibits the growth and motility of triple-negative breast cancer cells

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Cited by 170 publications
(135 citation statements)
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“…Paclitaxel may have different mechanism of cell apoptosis but earlier studies demonstrated reduced cytotoxicity in HER2 (human epidermal growth factor receptor 2) overexpressing breast cancer cells [38]. Recent studies demonstrated that piperine inhibited the growth of breast cancer cell lines in triple negative breast cancer [39], as well as those with estrogen receptorpositive breast cancer, via an antiproliferative effect and induction of caspase-dependent apoptosis [40]. Based on the above data and results, we hypothize that the mechanism of synergy interaction of the combinations of piperine and paclitaxel may involve an EGFR (epidermal growth factor receptor) signaling blockade.…”
Section: Discussionmentioning
confidence: 98%
“…Paclitaxel may have different mechanism of cell apoptosis but earlier studies demonstrated reduced cytotoxicity in HER2 (human epidermal growth factor receptor 2) overexpressing breast cancer cells [38]. Recent studies demonstrated that piperine inhibited the growth of breast cancer cell lines in triple negative breast cancer [39], as well as those with estrogen receptorpositive breast cancer, via an antiproliferative effect and induction of caspase-dependent apoptosis [40]. Based on the above data and results, we hypothize that the mechanism of synergy interaction of the combinations of piperine and paclitaxel may involve an EGFR (epidermal growth factor receptor) signaling blockade.…”
Section: Discussionmentioning
confidence: 98%
“…A combination of piperine and γ radiation exerted more cytotoxicity for triple negative breast cancer cells than γ radiation alone. Piperine inhibited the growth of triple negative breast cancer xenografts in immune-deficient mice [189]. …”
Section: Black Pepper and Piperinementioning
confidence: 99%
“…Recently, Zhang et al [25] demonstrated the chemopreventive abilities of piperine against two osteosarcoma cell lines (HOS and U-2OS) metastasis and Greenshields et al [40] demonstrated its protective properties against cancer cell migration in vitro through the inhibition of matrix metalloproteinase-2 and -9 expression.…”
Section: Introductionmentioning
confidence: 99%