6-Gingerol suppresses cell viability, migration and invasion via inhibiting EMT, and inducing autophagy and ferroptosis in LPS-stimulated and LPS-unstimulated prostate cancer cells

被引:37
作者
Liu, Chi-Ming [1 ,5 ]
An, Lijie [1 ,2 ]
Wu, Zhengping [3 ]
Ouyang, Ai-Jun [4 ]
Su, Mengqiao [1 ,2 ]
Shao, Zichen [1 ,2 ]
Lin, Yi [3 ]
Liu, Xiaoyu [3 ]
Jiang, Yinjie [1 ]
机构
[1] Yichun Univ, Sch Med, Yichun 336000, Jiangxi, Peoples R China
[2] Yichun Univ, Coll Chem & Bioengn, Yichun 336000, Jiangxi, Peoples R China
[3] Yichun Univ, Sch Aesthet Med, Yichun 336000, Jiangxi, Peoples R China
[4] Nanchang Univ, Affiliated Hosp 1, Dept Pharm, Nanchang 330006, Jiangxi, Peoples R China
[5] Yichun Univ, Sch Med, 576 XueFu Rd, Yichun 336000, Jiangxi, Peoples R China
关键词
6-gingerol; epithelial-mesenchymal transition; ferroptosis; autophagy; prostate cancer; GINGER PHYTOCHEMICALS; PC-3; CELLS; DEATH; INFLAMMATION; APOPTOSIS;
D O I
10.3892/ol.2022.13307
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
6-Gingerol is a bioactive compound isolated from Zingiber officinale. 6-Gingerol has been shown to have anticancer effects in numerous types of cancer cell. The mechanisms underlying the anticancer effect of 6-Gingerol in prostate cancer requires investigation. In the present study, the effect on cell viability of 6-Gingerol on LNCaP, PC3 and DU145 prostate cancer cells were determined using the MTT and colony formation assays. 6-Gingerol significantly inhibited cell migration, adhesion and invasion in LPS-stimulated and LPS-unstimulated prostate cancer cells. Furthermore, these changes were accompanied by alterations in the protein expression levels of epithelial-mesenchymal transition biomarkers, including E-cadherin, N-cadherin, Vimentin and zonula occludens-1. 6-Gingerol also induced autophagy by significantly increasing LC3B-II and Beclin-1 protein expression levels in prostate cancer cells. Combining 6-Gingerol with LY294002, an autophagy inhibitor, significantly increased cell survival in DU145 cells. Furthermore, 6-Gingerol significantly decreased the protein expression levels of glutathione (GSH) peroxidase 4 and nuclear factor erythroid 2-related factor 2 in prostate cancer cells. Reactive oxygen species (ROS) levels were significantly increased but GSH levels were decreased following 6-Gingerol treatment in prostate cancer cells. Co-treatment with the ferroptosis inhibitor, ferrostatin-1, significantly increased cell viability and significantly decreased ROS levels in 6-Gingerol-treated cells. These results suggested that 6-Gingerol may have inhibited prostate cell cancer viability via the regulation of autophagy and ferroptosis. In addition, 6-Gingerol inhibited cell migration, adhesion and invasion via the regulation of EMT-related protein expression levels in LPS-stimulated and LPS-unstimulated prostate cancer cells. In conclusion, 6-Gingerol may induce protective autophagy, autophagic cell death and ferroptosis-mediated cell death in prostate cancer cells. These findings may provide a strategy for the treatment and prevention of prostate cancer.
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页数:11
相关论文
共 53 条
[1]   Elucidating the Role of Protandim and 6-Gingerol in Protection Against Osteoarthritis [J].
Abusarah, Jamilah ;
Benabdoune, Houda ;
Shi, Qin ;
Lussier, Bertrand ;
Martel-Pelletier, Johanne ;
Malo, Michel ;
Fernandes, Julio C. ;
de Souza, Fatima Pereira ;
Fahmi, Hassan ;
Benderdour, Mohamed .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2017, 118 (05) :1003-1013
[2]   6-Gingerol, an active constituent of ginger, attenuates lipopolysaccharide-induced oxidation, inflammation, cognitive deficits, neuroplasticity, and amyloidogenesis in rat [J].
Adetuyi, Babatunde Oluwafemi ;
Farombi, Ebenezer Olatunde .
JOURNAL OF FOOD BIOCHEMISTRY, 2021, 45 (04)
[3]   EMT, cancer stem cells and autophagy; The three main axes of metastasis [J].
Babaei, Ghader ;
Aziz, Shiva Gholizadeh-Ghaleh ;
Jaghi, Nasrin Zare Zavieyh .
BIOMEDICINE & PHARMACOTHERAPY, 2021, 133
[4]   Ginger Phytochemicals Exhibit Synergy to Inhibit Prostate Cancer Cell Proliferation [J].
Brahmbhatt, Meera ;
Gundala, Sushma R. ;
Asif, Ghazia ;
Shamsi, Shahab A. ;
Aneja, Ritu .
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL, 2013, 65 (02) :263-272
[5]   The Cancer Prevention, Anti-Inflammatory and Anti-Oxidation of Bioactive Phytochemicals Targeting the TLR4 Signaling Pathway [J].
Chen, Chung-Yi ;
Kao, Chiu-Li ;
Liu, Chi-Ming .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2018, 19 (09)
[6]   Erianin, a novel dibenzyl compound in Dendrobium extract, inhibits lung cancer cell growth and migration via calcium/calmodulin-dependent ferroptosis [J].
Chen, Peng ;
Wu, Qibiao ;
Feng, Jiao ;
Yan, Lili ;
Sun, Yitian ;
Liu, Shuiping ;
Xiang, Yu ;
Zhang, Mingming ;
Pan, Ting ;
Chen, Xiaying ;
Duan, Ting ;
Zhai, Lijuan ;
Zhai, Bingtao ;
Wang, Wengang ;
Zhang, Ruonan ;
Chen, Bi ;
Han, Xuemeng ;
Li, Yicong ;
Chen, Liuxi ;
Liu, Ying ;
Huang, Xingxing ;
Jin, Ting ;
Zhang, Wenzheng ;
Luo, Hong ;
Chen, Xiaohui ;
Li, Yongqiang ;
Li, Qiujie ;
Li, Guohua ;
Zhang, Qin ;
Zhuo, Lvjia ;
Yang, Zuyi ;
Tang, Huifen ;
Xie, Tian ;
Ouyang, Xiaoping ;
Sui, Xinbing .
SIGNAL TRANSDUCTION AND TARGETED THERAPY, 2020, 5 (01)
[7]   Ginsenoside Rb1 Ameliorates Autophagy of Hypoxia Cardiomyocytes from Neonatal Rats via AMP-Activated Protein Kinase Pathway [J].
Dai, Sheng-nan ;
Hou, Ai-jie ;
Zhao, Shu-mei ;
Chen, Xiao-ming ;
Huang, Hua-ting ;
Chen, Bo-han ;
Kong, Hong-liang .
CHINESE JOURNAL OF INTEGRATIVE MEDICINE, 2019, 25 (07) :521-528
[8]   Identification of a small molecule as inducer of ferroptosis and apoptosis through ubiquitination of GPX4 in triple negative breast cancer cells [J].
Ding, Yahui ;
Chen, Xiaoping ;
Liu, Can ;
Ge, Weizhi ;
Wang, Qin ;
Hao, Xin ;
Wang, Mengmeng ;
Chen, Yue ;
Zhang, Quan .
JOURNAL OF HEMATOLOGY & ONCOLOGY, 2021, 14 (01)
[9]   Targeting Epithelial-Mesenchymal Transition (EMT) to Overcome Drug Resistance in Cancer [J].
Du, Bowen ;
Shim, Joong Sup .
MOLECULES, 2016, 21 (07)
[10]  
El-Khattouti Abdelouahid, 2013, J Cell Death, V6, P37, DOI 10.4137/JCD.S11034