Apoptotic Cell Death Induced by ofLBP6A, Lipopolysaccharide Binding Protein Model Peptide, Derived from Paralichthy olivaceus on MKN-28 Cells

被引:1
作者
Kang, Chang-Won [1 ]
Kim, Nan-Hee [1 ]
Park, Nam Gyu [2 ]
Kim, Gun-Do [1 ]
机构
[1] Pukyong Natl Univ, Coll Nat Sci, Dept Microbiol, Busan 48513, South Korea
[2] Pukyong Natl Univ, Coll Fisheries Sci, Dept Biotechnol, Busan 48513, South Korea
关键词
apoptosis; caspase; gastric cancer; lipopolysaccharide binding protein (LBP); MKN-28; cells; PERMEABILITY-INCREASING PROTEIN; POLY(ADP-RIBOSE) POLYMERASE; CASPASE-ACTIVATION; DNA FRAGMENTATION; CRYSTAL-STRUCTURE; BCL-2; PATHWAYS; COMPLEX; FAMILY; RELEASE;
D O I
10.1002/ddr.21296
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The aim of this study was to evaluate the anti-cancer effects of lipopolysaccharide binding protein (LBP) analogs derived from the marine resource Paralichthy olivaceus on MKN-28 gastric cancer cells. Five LBP analogs were used: ofLBP1N, ofLBP2A, ofLBP4N, ofLBP5A, and ofLBP6A. ofLBP6A induced cell death of MKN-28 cells at a concentration of 40 M. While the anti-proliferation effects ofLBP6A showed on MKN-28 cells at concentration of 40 M, it did not affect non-cancerous HEK-293 cells at the same concentration. The mechanism study showed that ofLBP6A lead to the inhibition of cell proliferation by apoptosis along with morphological changes. The phosphorylation of Fas associated death domain (FADD) as well as the expressions of cleaved caspase-8, -7, and -3 were increased by ofLBP6A treatment. Increased the expression level of cleaved caspase-3 was confirmed by immunofluorescence staining. The expressions of Bid, Bax, and cytochrome C were also increased by the treatment. However, the expressions of cellular FLICE (FADD-like IL-1-converting enzyme)-inhibitory protein (FLIP), Bcl-XL, and Bcl-2 were decreased by ofLBP6A treatment. The results of this study were the first to demonstrate the apoptotic anti-cancer effects of ofLBP6A, derived from P. olivavaceus on gastric cancer cells. Drug Dev Res 77 : 94-102, 2016. (c) 2016 Wiley Periodicals, Inc.
引用
收藏
页码:94 / 102
页数:9
相关论文
共 38 条
[1]  
[Anonymous], 2018, ANTI-CANCER DRUG, DOI [DOI 10.3322/caac.20115, DOI 10.1097/CAD.0000000000000617]
[2]   Ligand-based targeting of apoptosis in cancer: The potential of recombinant human apoptosis ligand 2/tumor necrosis factor-related apoptosis-inducing ligand (rhApo2L/TRAIL) [J].
Ashkenazi, Avi ;
Holland, Pamela ;
Eckhardt, S. Gail .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (21) :3621-3630
[3]   The tumor necrosis factor ligand and receptor families [J].
Bazzoni, F ;
Beutler, B .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (26) :1717-1725
[4]  
Bouillet P, 2002, J CELL SCI, V115, P1567
[5]   Biochemical pathways of caspase activation during apoptosis [J].
Budihardjo, I ;
Oliver, H ;
Lutter, M ;
Luo, X ;
Wang, XD .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 1999, 15 :269-290
[6]   Crystal structure of TRAIL-DR5 complex identifies a critical role of the unique frame insertion in conferring recognition specificity [J].
Cha, SS ;
Sung, BJ ;
Kim, YA ;
Song, YL ;
Kim, HJ ;
Kim, S ;
Lee, MS ;
Oh, BH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (40) :31171-31177
[7]   Curcumin induces apoptosis in human breast cancer cells through p53-dependent Bax induction [J].
Choudhuri, T ;
Pal, S ;
Agwarwal, ML ;
Das, T ;
Sa, G .
FEBS LETTERS, 2002, 512 (1-3) :334-340
[8]   Caspases: the executioners of apoptosis [J].
Cohen, GM .
BIOCHEMICAL JOURNAL, 1997, 326 :1-16
[9]   The BCL2 family: Regulators of the cellular life-or-death switch [J].
Cory, S ;
Adams, JM .
NATURE REVIEWS CANCER, 2002, 2 (09) :647-656
[10]   Caspase-activation pathways in apoptosis and immunity [J].
Creagh, EM ;
Conroy, H ;
Martin, SJ .
IMMUNOLOGICAL REVIEWS, 2003, 193 (01) :10-21