Clinicopathological significance of stanniocalcin 2 gene expression in colorectal cancer

被引:60
作者
Ieta, Keisuke [1 ,2 ]
Tanaka, Fumiaki [1 ]
Yokobori, Takehiko [1 ,2 ]
Kita, Yoshiaki [1 ]
Haraguchi, Naotsugu [1 ]
Mimori, Koshi [1 ]
Kato, Hiroyuki [2 ]
Asao, Takayuki [2 ]
Inoue, Hiroshi [1 ]
Kuwano, Hiroyuki [2 ]
Mori, Masaki [1 ]
机构
[1] Kyushu Univ, Dept Surg & Mol Oncol, Med Inst Bioregulat, Beppu, Oita 8740838, Japan
[2] Gunma Univ, Dept Gen Surg Sci, Grad Sch Med, Maebashi, Gunma 371, Japan
基金
日本学术振兴会; 日本科学技术振兴机构;
关键词
colorectal cancer; Stanniocalcin 2 (STC2); microarray; laser microdissection (LMD); MESSENGER-RNA EXPRESSION; CLINICAL-SIGNIFICANCE; BREAST-CANCER; IDENTIFICATION; PROTEIN; CDNA; MICROARRAY; MICRODISSECTION; CARCINOGENESIS; LOCALIZATION;
D O I
10.1002/ijc.24453
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Laser microdissection (LMD) and microarray were used to identify genes associated with colorectal cancer. Stanniocalcin 2 (STC2) expression and clinicopathological significance in 139 clinical colorectal cancer samples were specifically investigated using real-time quantitative reverse transcription-polymerase chain reaction. A number of genes upregulated in colorectal cancer cells compared to normal colorectal epithelial cells were identified including STC2. STC2 gene expression in cancer tissue was higher than in corresponding normal colorectal epithelial tissue in 124 of 139 cases (89.2%, p < 0.01). Tumors with high STC2 expression showed higher frequencies of lymph node metastasis, lymphatic invasion, tumor depth, tumor size and AJCC Stage classification (p < 0.01). Patients with high STC2 expression also showed significantly worse overall survival rates than those with low STC2 expression (p < 0.01). Furthermore, STC2 gene appeared to be associated with colorectal cancer progression and may be a useful prognostic indicator for colorectal cancer. (C) 2009 UICC
引用
收藏
页码:926 / 931
页数:6
相关论文
共 40 条
[11]   Transcriptional and translational control in the mammalian unfolded protein response [J].
Harding, HP ;
Calfon, M ;
Urano, F ;
Novoa, I ;
Ron, D .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 2002, 18 :575-599
[12]   BAC clones related to prognosis in patients with esophageal squamous carcinoma: An array comparative genomic hybridization study [J].
Hirasaki, Shigeo ;
Noguchi, Tsuyoshi ;
Mimori, Koshi ;
Onuki, Junko ;
Morita, Keiko ;
Inoue, Hiroshi ;
Sugihara, Kenichi ;
Mori, Masaki ;
Hirano, Takashi .
ONCOLOGIST, 2007, 12 (04) :406-417
[13]   Identification of overexpressed genes in hepatocellular carcinoma, with special reference to ubiquitin-conjugating enzyme E2C gene expression [J].
Ieta, Keisuke ;
Ojima, Eiki ;
Tanaka, Fumiaki ;
Nakamura, Yoshito ;
Haraguchi, Naotsugu ;
Mimori, Koshi ;
Inoue, Hiroshi ;
Kuwano, Hiroyuki ;
Mori, Masaki .
INTERNATIONAL JOURNAL OF CANCER, 2007, 121 (01) :33-38
[14]  
Inoue H, 2002, CLIN CANCER RES, V8, P3475
[15]   Molecular cloning of a second human stanniocalcin homologue (STC2) [J].
Ishibashi, K ;
Miyamoto, K ;
Taketani, Y ;
Morita, K ;
Takeda, E ;
Sasaki, S ;
Imai, I .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 250 (02) :252-258
[16]   Prospect of a stanniocalcin endocrine/paracrine system in mammals [J].
Ishibashi, K ;
Imai, M .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2002, 282 (03) :F367-F375
[17]  
Ismail RS, 2000, CANCER RES, V60, P6744
[18]   Characterization of stanniocalcin 2, a novel target of the mammalian unfolded protein response with cytoprotective properties [J].
Ito, D ;
Walker, JR ;
Thompson, CS ;
Moroz, I ;
Lin, W ;
Veselits, ML ;
Hakim, AM ;
Fienberg, AA ;
Thinakaran, G .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (21) :9456-9469
[19]   Stanniocalcin 1 and 2 are secreted as phosphoproteins from human fibrosarcoma cells [J].
Jellinek, DA ;
Chang, AC ;
Larsen, MR ;
Wang, X ;
Robinson, PJ ;
Reddel, RR .
BIOCHEMICAL JOURNAL, 2000, 350 :453-461
[20]   Cancer statistics, 2008 [J].
Jemal, Ahmedin ;
Siegel, Rebecca ;
Ward, Elizabeth ;
Hao, Yongping ;
Xu, Jiaquan ;
Murray, Taylor ;
Thun, Michael J. .
CA-A CANCER JOURNAL FOR CLINICIANS, 2008, 58 (02) :71-96