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In vitro ANTI-CANCER EFFECTS OF QUERCETIN ON TRIPLE NEGATIVE BREAST CANCER CELL LINE

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Phytochemicals are widely being explored for their cancer preventive  properties in today’s oncotherapy. Quercetin is a major constituent of various  dietary products and its anti-cancer potential was explored on different cancer  cell lines. The present study was conducted to find out the anti-proliferative  effects of quercetin on human triple negative breast cancer cell line MDA-MB The anti-cancer potential of quercetin, nano-quercetin and doxorubicin  at various concentrations were assessed by cellular cytotoxicity (MTT) assay.  The IC50 values of quercetin, nano-quercetin and doxorubicin on MDA-MB 231 cell line were 394.8, 204.6 and 17.17 μM, respectively. In vitro anti-cancer  effects of these drugs were manifested as apoptosis and cellular toxicity. The  cytotoxicity was moderate in quercetin, remarkable in nano-quercetin and  strong in doxorubicin treatments. The in vitro anti-cancer effect of quercetin  was comparable with the standard drug doxorubicin. Considering the  potential side effects of doxorubicin, the quercetin might be explored with  further studies in the treatment of mammary tumours in animals and humans.  
Title: In vitro ANTI-CANCER EFFECTS OF QUERCETIN ON TRIPLE NEGATIVE BREAST CANCER CELL LINE
Description:
Phytochemicals are widely being explored for their cancer preventive  properties in today’s oncotherapy.
Quercetin is a major constituent of various  dietary products and its anti-cancer potential was explored on different cancer  cell lines.
The present study was conducted to find out the anti-proliferative  effects of quercetin on human triple negative breast cancer cell line MDA-MB The anti-cancer potential of quercetin, nano-quercetin and doxorubicin  at various concentrations were assessed by cellular cytotoxicity (MTT) assay.
  The IC50 values of quercetin, nano-quercetin and doxorubicin on MDA-MB 231 cell line were 394.
8, 204.
6 and 17.
17 μM, respectively.
In vitro anti-cancer  effects of these drugs were manifested as apoptosis and cellular toxicity.
The  cytotoxicity was moderate in quercetin, remarkable in nano-quercetin and  strong in doxorubicin treatments.
The in vitro anti-cancer effect of quercetin  was comparable with the standard drug doxorubicin.
Considering the  potential side effects of doxorubicin, the quercetin might be explored with  further studies in the treatment of mammary tumours in animals and humans.
  .

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