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甘草查尔酮 A 通过自噬和 ATM-Chk2 激活抑制骨肉瘤细胞的增殖。

Licochalcone A Suppresses the Proliferation of Osteosarcoma Cells through Autophagy and ATM-Chk2 Activation.

机构信息

Department of Orthopedic Surgery, Changhua Christian Hospital, Changhua 50006, Taiwan.

Orthopedics & Sports Medicine Laboratory, Changhua Christian Hospital, Changhua 50006, Taiwan.

出版信息

Molecules. 2019 Jul 2;24(13):2435. doi: 10.3390/molecules24132435.

Abstract

Licochalcone A, a flavonoid extracted from licorice root, has been shown to exhibit broad anti-inflammatory, anti-bacterial, anticancer, and antioxidative bioactivity. In this study, we investigated the antitumor activity of Licochalcone A against human osteosarcoma cell lines. The data showed that Licochalcone A significantly suppressed cell viability in MTT assay and colony formation assay in osteosarcoma cell lines. Exposure to Licochalcone A blocked cell cycle progression at the G2/M transition and induced extrinsic apoptotic pathway in osteosarcoma cell lines. Furthermore, we found the Licochalcone A exposure resulted in rapid ATM and Chk2 activation, and high levels of nuclear foci of phosphorylated Chk2 at Thr 68 site in osteosarcoma cell lines. In addition, Licochalcone A exposure significantly induced autophagy in osteosarcoma cell lines. When Licochalcone A-induced autophagy was blocked by the autophagy inhibitor chloroquine, the expression of activated caspase-3 and Annexin V positive cells were reduced, and cell viability was rescued in Licochalcone A-treated osteosarcoma cell lines. These data indicate that the activation of ATM-Chk2 checkpoint pathway and autophagy may contribute to Licochalcone A-induced anti-proliferating effect in osteosarcoma cell lines. Our findings display the possibility that Licochalcone A may serve as a potential therapeutic agent against osteosarcoma.

摘要

甘草查尔酮 A 是从甘草根中提取的一种类黄酮,具有广泛的抗炎、抗菌、抗癌和抗氧化生物活性。在本研究中,我们研究了甘草查尔酮 A 对人骨肉瘤细胞系的抗肿瘤活性。结果表明,甘草查尔酮 A 显著抑制 MTT 检测和集落形成实验中的骨肉瘤细胞活力。甘草查尔酮 A 暴露可阻断细胞周期在 G2/M 期进展,并诱导骨肉瘤细胞系中的细胞外凋亡途径。此外,我们发现甘草查尔酮 A 暴露导致 ATM 和 Chk2 的快速激活,以及骨肉瘤细胞系中 Thr68 位点磷酸化 Chk2 的核焦点水平升高。此外,甘草查尔酮 A 暴露可显著诱导骨肉瘤细胞系中的自噬。当自噬抑制剂氯喹阻断甘草查尔酮 A 诱导的自噬时,激活的 caspase-3 和 Annexin V 阳性细胞的表达减少,甘草查尔酮 A 处理的骨肉瘤细胞系中的细胞活力得到挽救。这些数据表明,ATM-Chk2 检查点通路和自噬的激活可能有助于甘草查尔酮 A 诱导骨肉瘤细胞系的抗增殖作用。我们的研究结果显示,甘草查尔酮 A 可能作为骨肉瘤的潜在治疗剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e16/6651087/5407252ed831/molecules-24-02435-g001.jpg

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