Pentagamavunon-1 (PGV-1) inhibits ROS metabolic enzymes and suppresses tumor cell growth by inducing M phase (prometaphase) arrest and cell senescence

被引:35
作者
Lestari, Beni [1 ]
Nakamae, Ikuko [1 ]
Yoneda-Kato, Noriko [1 ]
Morimoto, Tsumoru [2 ]
Kanaya, Shigehiko [3 ]
Yokoyama, Takashi [1 ]
Shionyu, Masafumi [4 ]
Shirai, Tsuyoshi [4 ]
Meiyanto, Edy [5 ]
Kato, Jun-ya [1 ]
机构
[1] Nara Inst Sci & Technol, Grad Sch Sci & Technol, Div Biol Sci, Lab Tumor Cell Biol, Nara, Japan
[2] Nara Inst Sci & Technol, Grad Sch Sci & Technol, Div Mat Sci, Lab Synthet Organ Chem, Nara, Japan
[3] Nara Inst Sci & Technol, Grad Sch Sci & Technol, Div Informat Sci, Lab Computat Syst Biol, Nara, Japan
[4] Nagahama Inst Biosci & Technol, Nagahama, Japan
[5] Univ Gadjah Mada, Fac Pharm, CancerChemoprevent Res Ctr, Yogyakarta, Indonesia
关键词
CHRONIC MYELOID-LEUKEMIA; CYCLE ARREST; G2/M ARREST; OXIDATIVE STRESS; CURCUMIN; CANCER; IMATINIB; BINDING; AGENTS; SUFFICIENT;
D O I
10.1038/s41598-019-51244-3
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We previously showed that curcumin, a phytopolyphenol found in turmeric (Curcuma longa), targets a series of enzymes in the ROS metabolic pathway, induces irreversible growth arrest, and causes apoptosis. In this study, we tested Pentagamavunon-1 (PGV-1), a molecule related to curcumin, for its inhibitory activity on tumor cells in vitro and in vivo. PGV-1 exhibited 60 times lower GI(50) compared to that of curcumin in K562 cells, and inhibited the proliferation of cell lines derived from leukemia, breast adenocarcinoma, cervical cancer, uterine cancer, and pancreatic cancer. The inhibition of growth by PGV-1 remained after its removal from the medium, which suggests that PGV-1 irreversibly prevents proliferation. PGV-1 specifically induced prometaphase arrest in the M phase of the cell cycle, and efficiently induced cell senescence and cell death by increasing intracellular ROS levels through inhibition of ROS-metabolic enzymes. In a xenograft mouse model, PGV-1 had marked anti-tumor activity with little side effects by oral administration, whereas curcumin rarely inhibited tumor formation by this administration. Therefore, PGV-1 is a potential therapeutic to induce tumor cell apoptosis with few side effects and low risk of relapse.
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页数:12
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共 49 条
[1]   Glutathione transferases: substrates, inihibitors and pro-drugs in cancer and neurodegenerative diseases [J].
Allocati, Nerino ;
Masulli, Michele ;
Di Ilio, Carmine ;
Federici, Luca .
ONCOGENESIS, 2018, 7
[2]   Deceptive curcumin offers cautionary tale for chemists [J].
Baker, Monya .
NATURE, 2017, 541 (7636) :144-+
[3]   Announcing the worldwide Protein Data Bank [J].
Berman, H ;
Henrick, K ;
Nakamura, H .
NATURE STRUCTURAL BIOLOGY, 2003, 10 (12) :980-980
[4]   From in vitro to in vivo: intracellular determination of imatinib and nilotinib may be related with clinical outcome [J].
Bouchet, S. ;
Dulucq, S. ;
Pasquet, J-M ;
Lagarde, V. ;
Molimard, M. ;
Mahon, F-X .
LEUKEMIA, 2013, 27 (08) :1757-1759
[5]   Reaction mechanism of glyoxalase I explored by an X-ray crystallographic analysis of the human enzyme in complex with a transition state analogue [J].
Cameron, AD ;
Ridderström, M ;
Olin, B ;
Kavarana, MJ ;
Creighton, DJ ;
Mannervik, B .
BIOCHEMISTRY, 1999, 38 (41) :13480-13490
[6]   HIGH-EFFICIENCY TRANSFORMATION OF MAMMALIAN-CELLS BY PLASMID DNA [J].
CHEN, C ;
OKAYAMA, H .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (08) :2745-2752
[7]   Human 20α-hydroxysteroid dehydrogenase:: Crystallographic and site-directed mutagenesis studies lead to the identification of an alternative binding site for C21-steroids [J].
Couture, JF ;
Legrand, P ;
Cantin, L ;
Luu-The, V ;
Labrie, F ;
Breton, R .
JOURNAL OF MOLECULAR BIOLOGY, 2003, 331 (03) :593-604
[8]   Microtubule-binding agents: a dynamic field of cancer therapeutics [J].
Dumontet, Charles ;
Jordan, Mary Ann .
NATURE REVIEWS DRUG DISCOVERY, 2010, 9 (10) :790-803
[9]   Imatinib mesylate (Gleevec; STI571) monotherapy is ineffective in suppressing human anaplastic thyroid carcinoma cell growth in vitro [J].
Dziba, JM ;
Ain, KB .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (05) :2127-2135
[10]   Reactive carbonyls and oxidative stress: Potential for therapeutic intervention [J].
Ellis, Elizabeth M. .
PHARMACOLOGY & THERAPEUTICS, 2007, 115 (01) :13-24