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圆叶呋喃诱导肺癌细胞发生铁死亡和线粒体通透性转换。

Rotundifuran Induces Ferroptotic Cell Death and Mitochondria Permeability Transition in Lung Cancer Cells.

作者信息

Kang Myung-Ji, Moon Dong-Oh, Park Ji-Yoon, Kim Namho, Lee Su Hyeon, Ryu Hyung Won, Huh Yang Hoon, Lee Hyun-Sun, Kim Mun-Ock

机构信息

Natural Product Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Cheongju 28116, Republic of Korea.

Department of Biology Education, Daegu University, 201, Daegudae-ro, Gyeongsan-si 38453, Republic of Korea.

出版信息

Biomedicines. 2024 Mar 5;12(3):576. doi: 10.3390/biomedicines12030576.

DOI:10.3390/biomedicines12030576
PMID:38540189
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10968504/
Abstract

Rotundifuran (RF), a potent anti-inflammatory and anti-cancer compound, is a natural compound predominantly present in . Herein, we investigated the effects of RF on the growth of lung cancer cells. Our findings suggested that RF inhibits cell growth, highlighting its potential as a therapeutic agent for cancer treatment. Interestingly, we observed that cell growth inhibition was not due to apoptosis, as caspases were not activated and DNA fragmentation did not occur. Furthermore, we found that intracellular vacuoles and autophagy were induced, but RF-induced cell death was not affected when autophagy was inhibited. This prompted us to investigate other possible mechanisms underlying cell growth inhibition. Through a cDNA chip analysis, we confirmed changes in the expression of ferroptosis-related genes and observed lipid peroxidation. We further examined the effect of ferroptosis inhibitors and found that they alleviated cell growth inhibition induced by RF. We also observed the involvement of calcium signaling, ROS accumulation, and JNK signaling in the induction of ferroptosis. Our findings suggested that RF is a potent anti-cancer drug and further studies are needed to validate its clinal use.

摘要

圆叶呋喃(RF)是一种具有强大抗炎和抗癌作用的化合物,是一种主要存在于……的天然化合物。在此,我们研究了RF对肺癌细胞生长的影响。我们的研究结果表明,RF抑制细胞生长,凸显了其作为癌症治疗药物的潜力。有趣的是,我们观察到细胞生长抑制并非由凋亡引起,因为半胱天冬酶未被激活且未发生DNA片段化。此外,我们发现诱导了细胞内空泡和自噬,但抑制自噬时RF诱导的细胞死亡并未受到影响。这促使我们研究细胞生长抑制背后的其他可能机制。通过cDNA芯片分析,我们证实了铁死亡相关基因表达的变化并观察到脂质过氧化。我们进一步研究了铁死亡抑制剂的作用,发现它们减轻了RF诱导的细胞生长抑制。我们还观察到钙信号传导、活性氧积累和JNK信号传导参与了铁死亡的诱导。我们的研究结果表明,RF是一种有效的抗癌药物,需要进一步研究以验证其临床应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd80/10968504/a5d6f0032075/biomedicines-12-00576-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd80/10968504/d953f41638bc/biomedicines-12-00576-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd80/10968504/97cd71dc394c/biomedicines-12-00576-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd80/10968504/c841f078bfe1/biomedicines-12-00576-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd80/10968504/fb9816d88471/biomedicines-12-00576-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd80/10968504/e90cf10c9d1b/biomedicines-12-00576-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd80/10968504/a5d6f0032075/biomedicines-12-00576-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd80/10968504/d953f41638bc/biomedicines-12-00576-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd80/10968504/97cd71dc394c/biomedicines-12-00576-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd80/10968504/c841f078bfe1/biomedicines-12-00576-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd80/10968504/fb9816d88471/biomedicines-12-00576-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd80/10968504/e90cf10c9d1b/biomedicines-12-00576-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd80/10968504/a5d6f0032075/biomedicines-12-00576-g006.jpg

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