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白花丹醌通过PI3K/Akt信号通路诱导子宫内膜癌Ishikawa细胞周期阻滞、自噬和凋亡。

Plumbagin induces Ishikawa cell cycle arrest, autophagy, and apoptosis via the PI3K/Akt signaling pathway in endometrial cancer.

作者信息

Zhang Xiangsheng, Kan Huan, Liu Yun, Ding Wu

机构信息

College of Food Science and Engineering, Northwest A&F University, Yangling, 712100, China.

Key Laboratory for Forest Resources Conservation and Utilization in the Southwest Mountains of China, Ministry of Education, Southwest Forestry University, Kunming, 650224, China.

出版信息

Food Chem Toxicol. 2021 Feb;148:111957. doi: 10.1016/j.fct.2020.111957. Epub 2020 Dec 28.

Abstract

Plumbagin (PLB) is a naphthoquinone endowed with potential medicinal properties, including anticancer activities. We evaluated the effects of PLB on the viability, cell cycle, autophagy, and apoptosis of endometrial carcinoma Ishikawa cells. The proliferation of cells was significantly inhibited by PLB at 0, 8, 10, and 12 μM. By up regulating the expression of p53 and p21, PLB could block the cell cycle in G2/M phase and down regulate cyclin dependent kinase. The apoptosis in the cancer cells was characterized by noticeable chromatin edge collection, nuclear membrane expansion, and vacuolization. PLB could significantly induce autophagy in cells, and its inhibition ability and apoptosis induction were weakened by the autophagy inhibitor SBI-0206965. Our study suggested that PLB may exert anticancer effects by abrogating PI3K/Akt pathway, which recommends it as a promising future phytotherapeutic candidate for EC treatment.

摘要

白花丹醌(PLB)是一种具有潜在药用特性的萘醌,包括抗癌活性。我们评估了PLB对子宫内膜癌 Ishikawa 细胞的活力、细胞周期、自噬和凋亡的影响。在0、8、10和12 μM浓度下,PLB显著抑制细胞增殖。通过上调p53和p21的表达,PLB可将细胞周期阻滞在G2/M期,并下调细胞周期蛋白依赖性激酶。癌细胞的凋亡表现为明显的染色质边缘聚集、核膜扩张和空泡化。PLB可显著诱导细胞自噬,自噬抑制剂SBI-0206965可削弱其抑制能力和凋亡诱导作用。我们的研究表明,PLB可能通过废除PI3K/Akt通路发挥抗癌作用,这表明它有望成为未来治疗子宫内膜癌的植物治疗候选药物。

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