Anti-Cancer Natural Products and Their Bioactive Compounds Inducing ER Stress-Mediated Apoptosis: A Review

被引:390
作者
Kim, Changmin [1 ]
Kim, Bonglee [1 ]
机构
[1] Kyung Hee Univ, Dept Pathol, Coll Korean Med, Grad Sch, 1 Hoegi Dong, Seoul 130701, South Korea
基金
新加坡国家研究基金会;
关键词
natural products; bioactive compounds; cancer; endoplasmic-reticulum stress; unfolded protein response; apoptosis; ENDOPLASMIC-RETICULUM STRESS; UNFOLDED PROTEIN RESPONSE; BREAST-CANCER CELLS; MITOCHONDRIA-DEPENDENT PATHWAYS; HUMAN HEPATOCELLULAR-CARCINOMA; REFRACTORY PROSTATE CANCERS; OXYGEN SPECIES GENERATION; TRAIL-INDUCED APOPTOSIS; HUMAN LUNG-CANCER; OXIDATIVE STRESS;
D O I
10.3390/nu10081021
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Cancer is the second biggest cause of death worldwide. Despite a number of studies being conducted, the effective mechanism for treating cancer has not yet been fully understood. The tumor-microenvironment such as hypoxia, low nutrients could disturb function of endoplasmic reticulum (ER) to maintain cellular homeostasis, ultimately leading to the accumulation of unfolded proteins in ER, so-called ER stress. The ER stress has a close relation with cancer. ER stress initiates unfolded protein response (UPR) to re-establish ER homeostasis as an adaptive pathway in cancer. However, persistent ER stress triggers the apoptotic pathway. Therefore, blocking the adaptive pathway of ER stress or facilitating the apoptotic pathway could be an anti-cancer strategy. Recently, natural products and their derivatives have been reported to have anti-cancer effects via ER stress. Here, we address mechanisms of ER stress-mediated apoptosis and highlight strategies for cancer therapy by utilizing ER stress. Furthermore, we summarize anti-cancer activity of the natural products via ER stress in six major types of cancers globally (lung, breast, colorectal, gastric, prostate and liver cancer). This review deepens the understanding of ER stress mechanisms in major cancers as well as the suppressive impact of natural products against cancers via ER stress.
引用
收藏
页数:29
相关论文
共 180 条
[1]  
Abcouwer SF, 2002, INVEST OPHTH VIS SCI, V43, P2791
[2]   XBP1 controls diverse cell type- and condition-specific transcriptional regulatory networks [J].
Acosta-Alvear, Diego ;
Zhou, Yiming ;
Blais, Alexandre ;
Tsikitis, Mary ;
Lents, Nathan H. ;
Arias, Carolina ;
Lennon, Christen J. ;
Kluger, Yuval ;
Dynlacht, Brian David .
MOLECULAR CELL, 2007, 27 (01) :53-66
[3]   Ultrafine particles of Ulmus davidiana var. japonica induce apoptosis of gastric cancer cells via activation of caspase and endoplasmic reticulum stress [J].
Ahn, Joungjwa ;
Lee, Jong Suk ;
Yang, Kyung Mi .
ARCHIVES OF PHARMACAL RESEARCH, 2014, 37 (06) :783-792
[4]   Prevention and Management of Bone Metastases in Lung Cancer A Review [J].
Al Husaini, Hamed ;
Wheatley-Price, Paid ;
Clemons, Mark ;
Shepherd, Frances A. .
JOURNAL OF THORACIC ONCOLOGY, 2009, 4 (02) :251-259
[5]   Chaperone-Targeting Cytotoxin and Endoplasmic Reticulum Stress-Inducing Drug Synergize to Kill Cancer Cells [J].
Backer, Joseph M. ;
Krivoshein, Arcadius V. ;
Hamby, Carl V. ;
Pizzonia, John ;
Gilbert, Kenneth S. ;
Ray, Yonaton S. ;
Brand, Harrison ;
Paton, Adrienne W. ;
Paton, James C. ;
Backer, Marina V. .
NEOPLASIA, 2009, 11 (11) :1165-U72
[6]   ER stress-regulated translation increases tolerance to extreme hypoxia and promotes tumor growth [J].
Bi, MX ;
Naczki, C ;
Koritzinsky, M ;
Fels, D ;
Blais, J ;
Hu, NP ;
Harding, H ;
Novoa, I ;
Varia, M ;
Raleigh, J ;
Scheuner, D ;
Kaufman, RJ ;
Bell, J ;
Ron, D ;
Wouters, BG ;
Koumenis, C .
EMBO JOURNAL, 2005, 24 (19) :3470-3481
[7]   Perk-dependent translational regulation promotes tumor cell adaptation and angiogenesis in response to hypoxic stress [J].
Blais, Jaime D. ;
Addison, Christina L. ;
Edge, Robert ;
Falls, Theresa ;
Zhao, Huijun ;
Wary, Kishore ;
Koumenis, Costas ;
Harding, Heather P. ;
Ron, David ;
Holcik, Martin ;
Bell, John C. .
MOLECULAR AND CELLULAR BIOLOGY, 2006, 26 (24) :9517-9532
[8]   PERK promotes cancer cell proliferation and tumor growth by limiting oxidative DNA damage [J].
Bobrovnikova-Marjon, E. ;
Grigoriadou, C. ;
Pytel, D. ;
Zhang, F. ;
Ye, J. ;
Koumenis, C. ;
Cavener, D. ;
Diehl, J. A. .
ONCOGENE, 2010, 29 (27) :3881-3895
[9]  
Boelens J, 2007, IN VIVO, V21, P215
[10]   Opinion - The role of apoptosis in cancer development and treatment response [J].
Brown, JM ;
Attardi, LD .
NATURE REVIEWS CANCER, 2005, 5 (03) :231-237