Regulation of tumor necrosis factor-related apoptosis-inducing ligand-induced apoptosis by DJ-1 in thyroid cancer cells

被引:24
作者
Zhang, Hai-Yan [2 ]
Wang, Hua-Qin [1 ]
Liu, Hai-Mei [3 ]
Guan, Yifu [1 ]
Du, Zhen-Xian [4 ]
机构
[1] China Med Univ, Dept Biochem & Mol Biol, Shenyang 110001, Peoples R China
[2] China Med Univ, Dept Geriatr, Affiliated Hosp 1, Shenyang 110001, Peoples R China
[3] China Med Univ, Dept Anesthesiol, Affiliated Hosp 1, Shenyang 110001, Peoples R China
[4] China Med Univ, Dept Endocrinol & Metab, Affiliated Hosp 1, Shenyang 110001, Peoples R China
关键词
D O I
10.1677/ERC-07-0195
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
DJ-1, a cancer-associated protein protects cells from multiple toxic stresses. The expression of DJ-1 and its influence on thyroid cancer cell death has not been investigated so far. We analyzed DJ-1 expression in human thyroid carcinoma cell lines and the effect of DJ-1 on tumor necrosis factor-related apoptosis-inducing ligand (TRAIL)-induced apoptosis. DJ-1 was expressed in human thyroid carcinoma cell lines; small interfering RNA-mediated downregulation of its levels significantly sensitized thyroid carcinoma cells to TRAIL-induced apoptosis, whereas the forced exogenous expression of DJ-1 significantly suppressed cell death induced by TRAIL. We also report here that TRAIL-induced thyroid cancer cell apoptosis is mediated by oxidative stress and that DJ-1, a potent nutritional antioxidant, protects cancer cells from apoptosis at least in part by impeding the elevation of reactive oxygen species levels induced by TRAIL and impairing caspase-8 activation. Subsequently, we investigated DJ-1 expression in 52 normal and 74 primary thyroid carcinomas from patients of China Medical University. The protein was not detectable in the 52 specimens of normal thyroid, while 70 out of 74 analyzed carcinomas (33 out of 33 follicular, 17 out of 19 papillary, 12 out of 13 medullar, and 8 out of 9 anaplastic) were clearly positive for DJ-1 expression. Our data demonstrated that DJ-1 is specifically expressed in thyroid carcinomas and not in the normal thyroid tissue. In addition, the protein modulates the response to TRAIL-mediated apoptosis in human neoplastic thyroid cells, at least partially through its antioxidant property.
引用
收藏
页码:535 / 544
页数:10
相关论文
共 37 条
[1]   Crosstalk between extrinsic and intrinsic cell death pathways in pancreatic cancer: Synergistic action of estrogen metabolite and ligands of death receptor family [J].
Basu, A ;
Castle, VP ;
Bouziane, M ;
Bhalla, K ;
Haldar, S .
CANCER RESEARCH, 2006, 66 (08) :4309-4318
[2]   TRAIL receptor-2 signals apoptosis through FADD and caspase-8 [J].
Bodmer, JL ;
Holler, N ;
Reynard, S ;
Vinciguerra, P ;
Schneider, P ;
Juo, P ;
Blenis, J ;
Tschopp, J .
NATURE CELL BIOLOGY, 2000, 2 (04) :241-243
[3]   Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism [J].
Bonifati, V ;
Rizzu, P ;
van Baren, MJ ;
Schaap, O ;
Breedveld, GJ ;
Krieger, E ;
Dekker, MCJ ;
Squitieri, F ;
Ibanez, P ;
Joosse, M ;
van Dongen, JW ;
Vanacore, N ;
van Swieten, JC ;
Brice, A ;
Meco, G ;
van Duijn, CM ;
Oostra, BA ;
Heutink, P .
SCIENCE, 2003, 299 (5604) :256-259
[4]   DJ-1, a cancer- and Parkinson's disease-associated protein, stabilizes the antioxidant transcriptional master regulator Nrf2 [J].
Clements, Casey M. ;
McNally, Richard S. ;
Conti, Brian J. ;
Mak, Tak W. ;
Ting, Jenny P-Y. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (41) :15091-15096
[5]   Pathways to parkinsonism [J].
Cookson, MR .
NEURON, 2003, 37 (01) :7-10
[6]   Glutamine prevents cytokine-induced apoptosis in human colonic epithelial cells [J].
Evans, ME ;
Jones, DP ;
Ziegler, TR .
JOURNAL OF NUTRITION, 2003, 133 (10) :3065-3071
[7]  
Grzmil M, 2004, INT J ONCOL, V24, P97
[8]   Differential control of apoptogis by DJ-1 in prostate benign and cancer cells [J].
Hod, Y .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2004, 92 (06) :1221-1233
[9]  
Hod Y, 1999, J CELL BIOCHEM, V72, P435, DOI 10.1002/(SICI)1097-4644(19990301)72:3<435::AID-JCB12>3.3.CO
[10]  
2-8