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1
Correction: Hseu, Y.-C., et al. The In Vitro and In Vivo Anticancer Properties of Chalcone Flavokawain B through Induction of ROS-Mediated Apoptotic and Autophagic Cell Death in Human Melanoma Cells. 2020, , 2936.
Cancers (Basel). 2021 Jan 15;13(2):303. doi: 10.3390/cancers13020303.
2
Flavokawain B, a novel chalcone from Alpinia pricei Hayata with potent apoptotic activity: Involvement of ROS and GADD153 upstream of mitochondria-dependent apoptosis in HCT116 cells.普那霉素 B，一种来自高良姜的新型查尔酮，具有很强的凋亡活性：在 HCT116 细胞中线粒体依赖性凋亡中涉及 ROS 和 GADD153 的上游。
Free Radic Biol Med. 2010 Jul 15;49(2):214-26. doi: 10.1016/j.freeradbiomed.2010.04.005. Epub 2010 Apr 14.
3
Chalcone flavokawain B induces autophagic-cell death via reactive oxygen species-mediated signaling pathways in human gastric carcinoma and suppresses tumor growth in nude mice.查尔酮 flavokawain B 通过活性氧介导的信号通路诱导人胃癌细胞发生自噬性细胞死亡，并抑制裸鼠肿瘤生长。
Arch Toxicol. 2017 Oct;91(10):3341-3364. doi: 10.1007/s00204-017-1967-0. Epub 2017 Apr 3.
4
Flavokawain B inhibits growth of human squamous carcinoma cells: Involvement of apoptosis and cell cycle dysregulation in vitro and in vivo.Flavokawain B 抑制人鳞状细胞癌细胞的生长：体外和体内的细胞凋亡和细胞周期失调的参与。
J Nutr Biochem. 2012 Apr;23(4):368-78. doi: 10.1016/j.jnutbio.2011.01.002. Epub 2011 May 2.
5
Flavokawain B and Doxorubicin Work Synergistically to Impede the Propagation of Gastric Cancer Cells via ROS-Mediated Apoptosis and Autophagy Pathways.黄樟素B与阿霉素协同作用，通过活性氧介导的凋亡和自噬途径抑制胃癌细胞的增殖。
Cancers (Basel). 2020 Sep 1;12(9):2475. doi: 10.3390/cancers12092475.
6
Flavokawain A, a novel chalcone from kava extract, induces apoptosis in bladder cancer cells by involvement of Bax protein-dependent and mitochondria-dependent apoptotic pathway and suppresses tumor growth in mice.黄烷卡瓦因A是一种从卡瓦提取物中分离出的新型查尔酮，它通过参与依赖Bax蛋白和线粒体的凋亡途径诱导膀胱癌细胞凋亡，并抑制小鼠肿瘤生长。
Cancer Res. 2005 Apr 15;65(8):3479-86. doi: 10.1158/0008-5472.CAN-04-3803.
7
Chalcone flavokawain A attenuates TGF-β1-induced fibrotic pathology via inhibition of ROS/Smad3 signaling pathways and induction of Nrf2/ARE-mediated antioxidant genes in vascular smooth muscle cells.查尔酮 flavokawain A 通过抑制 ROS/Smad3 信号通路和诱导 Nrf2/ARE 介导的抗氧化基因在血管平滑肌细胞中减轻 TGF-β1 诱导的纤维化病理。
J Cell Mol Med. 2019 Feb;23(2):775-788. doi: 10.1111/jcmm.13973. Epub 2018 Dec 13.
8
Induction of Apoptosis and Cell Cycle Arrest by Flavokawain C on HT-29 Human Colon Adenocarcinoma via Enhancement of Reactive Oxygen Species Generation, Upregulation of p21, p27, and GADD153, and Inactivation of Inhibitor of Apoptosis Proteins.黄樟素C通过增强活性氧生成、上调p21、p27和GADD153以及使凋亡抑制蛋白失活诱导HT-29人结肠腺癌细胞凋亡和细胞周期停滞
Pharmacogn Mag. 2017 Jul;13(Suppl 2):S321-S328. doi: 10.4103/0973-1296.210180. Epub 2017 Jul 11.
9
Suppression of LPS-Induced Inflammation by Chalcone Flavokawain A through Activation of Nrf2/ARE-Mediated Antioxidant Genes and Inhibition of ROS/NFB Signaling Pathways in Primary Splenocytes.姜黄素查尔酮 flavokawain A 通过激活 Nrf2/ARE 介导的抗氧化基因和抑制 ROS/NFB 信号通路抑制 LPS 诱导的原代脾细胞炎症。
Oxid Med Cell Longev. 2020 Jun 12;2020:3476212. doi: 10.1155/2020/3476212. eCollection 2020.
10
In vitro Toxicity and in vivo Immunomodulatory Effects of Flavokawain A and Flavokawain B in Balb/C Mice.黄樟素A和黄樟素B对Balb/C小鼠的体外毒性及体内免疫调节作用
Nat Prod Commun. 2015 Jul;10(7):1199-202.

引用本文的文献

1
The Induction of G2/M Phase Cell Cycle Arrest and Apoptosis by the Chalcone Derivative 1C in Sensitive and Resistant Ovarian Cancer Cells Is Associated with ROS Generation.查尔酮衍生物 1C 诱导敏感和耐药卵巢癌细胞 G2/M 期细胞周期阻滞和凋亡与 ROS 生成有关。
Int J Mol Sci. 2024 Jul 9;25(14):7541. doi: 10.3390/ijms25147541.

本文引用的文献

1
The In Vitro and In Vivo Anticancer Properties of Chalcone Flavokawain B through Induction of ROS-Mediated Apoptotic and Autophagic Cell Death in Human Melanoma Cells.查耳酮类黄酮卡瓦因B通过诱导活性氧介导的人黑色素瘤细胞凋亡和自噬性细胞死亡的体外和体内抗癌特性
Cancers (Basel). 2020 Oct 12;12(10):2936. doi: 10.3390/cancers12102936.

Correction: Hseu, Y.-C., et al. The In Vitro and In Vivo Anticancer Properties of Chalcone Flavokawain B through Induction of ROS-Mediated Apoptotic and Autophagic Cell Death in Human Melanoma Cells. 2020, , 2936.

作者信息

Hseu You-Cheng, Chiang Yu-Chi, Vudhya Gowrisankar Yugandhar, Lin Kai-Yuan, Huang Sheng-Teng, Shrestha Sirjana, Chang Geng-Ruei, Yang Hsin-Ling

机构信息

Department of Cosmeceutics, College of Pharmacy, China Medical University, Taichung 40402, Taiwan.

Department of Health and Nutrition Biotechnology, Asia University, Taichung 41354, Taiwan.

出版信息

Cancers (Basel). 2021 Jan 15;13(2):303. doi: 10.3390/cancers13020303.

DOI:10.3390/cancers13020303
PMID:33467786
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7830129/
Abstract

In the original article [...].

摘要