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白藜芦醇通过 PI3K/Akt/c-Myc 通路抑制小细胞肺癌 H446 细胞系的活力并诱导其凋亡。

Resveratrol inhibits viability and induces apoptosis in the small‑cell lung cancer H446 cell line via the PI3K/Akt/c‑Myc pathway.

机构信息

Department of Pulmonary and Critical Care Medicine, Tangdu Hospital, Air Force Military Medical University, Xi'an, Shaanxi 710038, P.R. China.

Department of Pulmonary and Critical Care Medicine, General Hospital of Western Theater Command, Chengdu, Sichuan 610083, P.R. China.

出版信息

Oncol Rep. 2020 Nov;44(5):1821-1830. doi: 10.3892/or.2020.7747. Epub 2020 Sep 1.


DOI:10.3892/or.2020.7747
PMID:32901891
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7550979/
Abstract

There have been no major breakthroughs in the treatment of small‑cell lung cancer (SCLC) in recent decades. It is thus essential to explore new or adjuvant treatment options for SCLC. Resveratrol (Res) is a natural antioxidant revealed to influence the entire process of cancer development. Accordingly, the present study used the SCLC cell line H446 to explore the antitumor mechanism of Res. Cells were treated with 40 µg/ml Res with or without pretreatment with the antioxidant N‑acetyl‑L‑cysteine (NAC). H446 cell viability and apoptosis were assessed with MTT and flow cytometry, and the expression of cytochrome c and the PI3K/Akt/c‑Myc pathway and the nuclear translocation of apoptosis inducing factor (AIF) were assessed by western blotting. In addition, the changes in ROS content and mitochondrial membrane potential were determined. The results revealed that Res inhibited H446 cell viability and induced apoptosis, increased cytochrome c expression, inhibited the expression of PI3K/Akt/c‑Myc signaling pathway components, and promoted the translocation of AIF from the cytoplasm to the nucleus in H446 cells. However, NAC pretreatment reversed these changes to various extents. The results of the present study indicated that Res may inhibit the viability and promote the apoptosis of human SCLC H446 cells through the PI3K/Akt/c‑Myc pathway and that oxidative stress and mitochondrial membrane potential depolarization may be involved in the aforementioned processes.

摘要

在过去的几十年中,小细胞肺癌(SCLC)的治疗没有取得重大突破。因此,探索 SCLC 的新治疗方法或辅助治疗方法至关重要。白藜芦醇(Res)是一种天然抗氧化剂,被发现会影响癌症发展的整个过程。因此,本研究使用 SCLC 细胞系 H446 来探索 Res 的抗肿瘤机制。用 40µg/ml 的 Res 处理细胞,并用抗氧化剂 N-乙酰-L-半胱氨酸(NAC)预处理或不预处理。用 MTT 和流式细胞术评估 H446 细胞活力和细胞凋亡,用 Western blot 评估细胞色素 c 和 PI3K/Akt/c-Myc 通路的表达以及凋亡诱导因子(AIF)的核易位。此外,还测定了 ROS 含量和线粒体膜电位的变化。结果表明,Res 抑制 H446 细胞活力并诱导细胞凋亡,增加细胞色素 c 的表达,抑制 PI3K/Akt/c-Myc 信号通路成分的表达,并促进 AIF 从细胞质向细胞核易位。然而,NAC 预处理在不同程度上逆转了这些变化。本研究结果表明,Res 可能通过 PI3K/Akt/c-Myc 通路抑制人 SCLC H446 细胞的活力并促进其凋亡,氧化应激和线粒体膜电位去极化可能参与上述过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f01/7550979/cab057087d78/OR-44-05-1821-g07.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f01/7550979/fb4ec60a332e/OR-44-05-1821-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f01/7550979/4359e454c4d0/OR-44-05-1821-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f01/7550979/3b387c74ea83/OR-44-05-1821-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f01/7550979/d83f10a3aac7/OR-44-05-1821-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f01/7550979/8686fd571f71/OR-44-05-1821-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f01/7550979/0df110bf226e/OR-44-05-1821-g05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f01/7550979/3f60bd57d426/OR-44-05-1821-g06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f01/7550979/cab057087d78/OR-44-05-1821-g07.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f01/7550979/fb4ec60a332e/OR-44-05-1821-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f01/7550979/4359e454c4d0/OR-44-05-1821-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f01/7550979/3b387c74ea83/OR-44-05-1821-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f01/7550979/d83f10a3aac7/OR-44-05-1821-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f01/7550979/8686fd571f71/OR-44-05-1821-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f01/7550979/0df110bf226e/OR-44-05-1821-g05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f01/7550979/3f60bd57d426/OR-44-05-1821-g06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f01/7550979/cab057087d78/OR-44-05-1821-g07.jpg

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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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本文引用的文献

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