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三氟拉嗪通过激活 AMPK/mTOR/ULK1 信号通路诱导骨肉瘤细胞发生线粒体自噬。

Trifluoperazine activates AMPK / mTOR / ULK1 signaling pathway to induce mitophagy in osteosarcoma cells.

机构信息

Department of Orthopedic Surgery, Zhongshan Hospital (Xiamen), Fudan University, Xiamen, 361000, China.

State Key Laboratory of Cellular Stress Biology, School of Medicine, Xiamen University, Xiamen, 361102, China.

出版信息

Chem Biol Interact. 2024 Apr 1;392:110904. doi: 10.1016/j.cbi.2024.110904. Epub 2024 Feb 13.

Abstract

Osteosarcoma is a prevalent kind of primary bone malignancy. Trifluoperazine, as an antipsychotic drug, has anti-tumor activity against a variety of cancers. Nevertheless, the impact of trifluoperazine on osteosarcoma is unclear. Our investigation aimed to explore the mechanism of trifluoperazine's effect on osteosarcoma. We found that trifluoperazine inhibited 143B and U2-OS osteosarcoma cell proliferation in a method based on the dose. Furthermore, it was shown that trifluoperazine induced the accumulation of reactive oxygen species (ROS) to cause mitochondrial damage and induced mitophagy in osteosarcoma cells. Finally, combined with RNA-seq results, we first demonstrated the AMPK/mTOR/ULK1 signaling pathway as a potential mechanism of trifluoperazine-mediated mitophagy in osteosarcoma cells and can be suppressed by AMPK inhibitor Compound C.

摘要

骨肉瘤是一种常见的原发性骨恶性肿瘤。三氟拉嗪作为一种抗精神病药物,对多种癌症具有抗肿瘤活性。然而,三氟拉嗪对骨肉瘤的影响尚不清楚。我们的研究旨在探讨三氟拉嗪对骨肉瘤的作用机制。我们发现三氟拉嗪通过剂量依赖的方式抑制 143B 和 U2-OS 骨肉瘤细胞的增殖。此外,研究表明三氟拉嗪诱导活性氧(ROS)的积累,导致线粒体损伤,并诱导骨肉瘤细胞发生线粒体自噬。最后,结合 RNA-seq 结果,我们首次证明 AMPK/mTOR/ULK1 信号通路是三氟拉嗪介导的骨肉瘤细胞自噬的潜在机制,并且可以被 AMPK 抑制剂 Compound C 抑制。

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