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首页> 外文期刊>Planta medica: Natural products and medicinal plant research >Mechanism of Ascorbate-Induced Cell Death in Human Pancreatic Cancer Cells: Role of Bcl-2, Beclin 1 and Autophagy
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Mechanism of Ascorbate-Induced Cell Death in Human Pancreatic Cancer Cells: Role of Bcl-2, Beclin 1 and Autophagy

机译:抗坏血酸诱导的人类胰腺癌细胞死亡的机制:Bcl-2,Beclin 1和自噬的作用。

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摘要

The present study investigates the anticancer effect of ascorbate in MIA-PaCa-2 human pancreatic cancer cells using both in vitro and in vivo models, with a focus on assessing the role of oxidative stress and autophagy as important mechanistic elements in its anticancer actions. We showed that ascorbate suppresses the growth of human pancreatic cancer cells via the induction of oxidative stress and caspase-independent cell death. Ascorbate induces the formation of autophagosomes and the presence of autophagy inhibitors suppresses ascorbate-induced cell death. These data suggest that the induction of autophagosome formation contributes to ascorbate-induced pancreatic cancer cell death.
机译:本研究使用体内和体外模型研究了抗坏血酸在MIA-PaCa-2人胰腺癌细胞中的抗癌作用,重点是评估氧化应激和自噬在其抗癌作用中的重要机制。我们表明,抗坏血酸通过诱导氧化应激和不依赖caspase的细胞死亡来抑制人胰腺癌细胞的生长。抗坏血酸诱导自噬体的形成,并且自噬抑制剂的存在抑制了抗坏血酸诱导的细胞死亡。这些数据表明自噬体形成的诱导有助于抗坏血酸诱导的胰腺癌细胞死亡。

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