NAIF1 is down-regulated in gastric cancer and promotes apoptosis through the caspase-9 pathway in human MKN45 cells

被引:15
作者
Luo, Qing
Zhao, Mei
Zhong, Jialing
Ma, Yiming
Deng, Guohua
Liu, Jian
Wang, Jia
Yuan, Xinghua
Huang, Changzhi [1 ,2 ,3 ]
机构
[1] Chinese Acad Med Sci, Canc Inst & Hosp, Dept Etiol & Carcinogenesis, Beijing 100021, Peoples R China
[2] Chinese Acad Med Sci, Canc Inst & Hosp, State Key Lab Mol Oncol, Beijing 100021, Peoples R China
[3] Peking Union Med Coll, Beijing 100021, Peoples R China
关键词
nuclear apoptosis-inducing factor 1; gastric cancer; apoptosis; caspase-9; SWIRM DOMAIN; BINDING; MOTIF; STATISTICS; THERAPY; CYCLE;
D O I
10.3892/or.2011.1171
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Many key proteins are down-regulated or lose their function during cancer genesis and accelerate the progress of cancer. We found that nuclear apoptosis-inducing factor 1 (NAIF1) was highly expressed in normal gastric tissues but was down-regulated or lost in gastric cancer tissues (P<0.001). NAIF1 expression was higher in well-differentiated (P=0.004) than in moderately- or poorly-differentiated gastric cancer. NAIF1 expression was associated with different T stages (P=0.024). In vitro, NAIF1 can inhibit tumor cell proliferation and induce G0/G1 phase cell cycle arrest in the MKN45 cell line. NAIF1 can induce apoptosis through activation of procaspase-9 rather than procaspase-8 followed by activation of the caspase-3 pathway. We designed and constructed two truncation mutants, pEGFP-N1-NLS and pEGFP-N1-GRR, and identified the N-terminal 1-90 amino acid domain of NAIF1, which is a helix-turn-helix motif and which was sufficient for inducing apoptosis. Therefore, these findings suggest that NAIF1 plays an inhibitory role in the initial steps of gastric cancer genesis and may provide new strategies for developing anti-cancer drugs using small molecular polypeptides.
引用
收藏
页码:1117 / 1123
页数:7
相关论文
共 29 条
[1]   Immunocytochemistry and protein analysis suggest that reptilian claws contain small high cysteine-glycine proteins [J].
Alibardi, L. ;
Toni, M. .
TISSUE & CELL, 2009, 41 (03) :180-192
[2]   Mechanisms of caspase activation [J].
Boatright, KM ;
Salvesen, GS .
CURRENT OPINION IN CELL BIOLOGY, 2003, 15 (06) :725-731
[3]   Targeted manipulation of apoptosis in cancer treatment [J].
Call, Justin A. ;
Eckhardt, S. Gail ;
Camidge, D. Ross .
LANCET ONCOLOGY, 2008, 9 (10) :1002-1011
[4]   Cancer: A cell cycle defect [J].
Foster, Irene .
RADIOGRAPHY, 2008, 14 (02) :144-149
[5]   Functional identification of the pro-apoptotic effector domain in human Sox4 [J].
Hur, EH ;
Hur, W ;
Choi, JY ;
Kim, IK ;
Kim, HY ;
Yoon, SK ;
Rhim, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 325 (01) :59-67
[6]   Gene expression analysis of terminal differentiation of human melanoma cells highlights global reductions in cell cycle-associated genes [J].
Huynh, Kim Mai ;
Kim, Gyoungmi ;
Kim, Dong-Joon ;
Yang, Suk-Jin ;
Park, Seong-Min ;
Yeom, Young-Il ;
Fisher, Paul B. ;
Kang, Dongchul .
GENE, 2009, 433 (1-2) :32-39
[7]   Cancer statistics, 2005 [J].
Jemal, A ;
Murray, T ;
Ward, E ;
Samuels, A ;
Tiwari, RC ;
Ghafoor, A ;
Feuer, EJ ;
Thun, MJ .
CA-A CANCER JOURNAL FOR CLINICIANS, 2005, 55 (01) :10-30
[8]   The TRAIL apoptotic pathway in cancer onset, progression and therapy [J].
Johnstone, Ricky W. ;
Frew, Ailsa J. ;
Smyth, Mark J. .
NATURE REVIEWS CANCER, 2008, 8 (10) :782-798
[9]   A P-LOOP RELATED MOTIF (GXXGXXK) HIGHLY CONSERVED IN SULFOTRANSFERASES IS REQUIRED FOR BINDING THE ACTIVATED SULFATE DONOR [J].
KOMATSU, K ;
DRISCOLL, WJ ;
KOH, YC ;
STROTT, CA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 204 (03) :1178-1185
[10]   Overexpression of the novel human gene, nuclear apoptosis-inducing factor 1, induces apoptosis [J].
Lv, BF ;
Shi, TP ;
Wang, XY ;
Song, QS ;
Zhang, YM ;
Shen, Y ;
Ma, DL ;
Lou, YX .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2006, 38 (04) :671-683