Induction of HITS, a newly identified family with sequence similarity 107 protein (FAM107B), in cancer cells by heat shock stimulation

被引:12
作者
Nakajima, Hideo [1 ]
Ishigaki, Yasuhito [2 ]
Xia, Qi-Sheng [1 ]
Ikeda, Takayuki [3 ]
Yoshitake, Yoshino [3 ]
Yonekura, Hideto [3 ]
Nojima, Takayuki [4 ]
Tanaka, Takuji [4 ]
Umehara, Hisanori [5 ]
Tomosugi, Naohisa [2 ]
Takata, Takanobu [2 ]
Shimasaki, Takeo [1 ]
Nakaya, Naoki [1 ]
Sato, Itaru [1 ]
Kawakami, Kazuyuki [6 ]
Koizumi, Keita [7 ]
Minamoto, Toshinari [6 ]
Motoo, Yoshiharu [1 ]
机构
[1] Kanazawa Med Univ, Dept Med Oncol, Kahoku, Ishikawa 9200293, Japan
[2] Kanazawa Med Univ, Inst Med Res, Kahoku, Ishikawa 9200293, Japan
[3] Kanazawa Med Univ, Dept Biochem, Kahoku, Ishikawa 9200293, Japan
[4] Kanazawa Med Univ, Dept Pathol, Kahoku, Ishikawa 9200293, Japan
[5] Kanazawa Med Univ, Dept Hematol & Immunol, Kahoku, Ishikawa 9200293, Japan
[6] Kanazawa Univ, Grad Sch Med Sci, Canc Res Inst, Div Translat & Clin Oncol, Kanazawa, Ishikawa 9200934, Japan
[7] Kanazawa Univ, Grad Sch Med Sci, Dept Biophys Genet, Kanazawa, Ishikawa 9200934, Japan
关键词
FAM107; TU3A; heat shock protein; tumor suppressor gene; HUMAN BREAST-CANCER; GASTRIC-CANCER; GERMLINE MUTATIONS; COLORECTAL-CANCER; PROSTATE-CANCER; BETA-CATENIN; GENE; EXPRESSION; CARCINOMA; ADENOCARCINOMA;
D O I
10.3892/ijo_00000707
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The Family with sequence similarity 107 (FAM107) possesses an N-terminal domain of unknown function (DUF1151) that is highly conserved beyond species. In human, FAM107A termed TU3A/DRR1 has been reported as a candidate tumor suppressor gene which expression is down-regulated in several types of cancer, however no studies have investigated the other family protein, FAM107B. In the present study, we designated FAM107B as heat shock-inducible tumor small protein (HITS) and studied its expression and functional properties in cancer. HITS is an 18-kDa nuclear protein expressed in a variety of tissues including stomach, colon, lung and lymphoid organs. In human gastric and colorectal cancers and a mouse model of colon cancer, its expression in tumor cells was much lower than normal epithelial cells, while expression pattern and intensity varied among different histological types of cancer. In functional analysis in vitro, forced expression of this protein suppresses the cellular responses to growth factors. Furthermore, HITS gene carries the promoter region providing heat shock transcription factor (HSF) binding sites and amplifying the transcription of HITS by heat shock or hyperthermia treatment both in vitro and in vivo. Thus HITS would be a potential tumor suppressor gene similar to TU3A containing heat responding elements, which contrasts with previously described oncogenic activities of other heat shock proteins such as HSP70 and HSP90.
引用
收藏
页码:583 / 593
页数:11
相关论文
共 48 条
[1]   Methylation-associated silencing of TU3A in human cancers [J].
Awakura, Yasuo ;
Nakamura, Eijiro ;
Ito, Noriyuki ;
Kamoto, Toshiyuki ;
Ogawa, Osamu .
INTERNATIONAL JOURNAL OF ONCOLOGY, 2008, 33 (04) :893-899
[2]   HEAT-SHOCK PROTEIN-HSP70 IN PATIENTS WITH AXILLARY LYMPH NODE-NEGATIVE BREAST-CANCER - PROGNOSTIC IMPLICATIONS [J].
CIOCCA, DR ;
CLARK, GM ;
TANDON, AK ;
FUQUA, SAW ;
WELCH, WJ ;
MCGUIRE, WL .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1993, 85 (07) :570-574
[3]  
CORREA P, 1992, CANCER RES, V52, P6735
[4]   Heat shock factor 1 is a powerful multifaceted modifier of carcinogenesis [J].
Dai, Chengkai ;
Whitesell, Luke ;
Rogers, Arlin B. ;
Lindquist, Susan .
CELL, 2007, 130 (06) :1005-1018
[5]   Interleukin-1 polymorphisms associated with increased risk of gastric cancer [J].
El-Omar, EM ;
Carrington, M ;
Chow, WH ;
McColl, KEL ;
Bream, JH ;
Young, HA ;
Herrera, J ;
Lissowska, J ;
Yuan, CC ;
Rothman, N ;
Lanyon, G ;
Martin, M ;
Fraumeni, JF ;
Rabkin, CS .
NATURE, 2000, 404 (6776) :398-402
[6]   A GENETIC MODEL FOR COLORECTAL TUMORIGENESIS [J].
FEARON, ER ;
VOGELSTEIN, B .
CELL, 1990, 61 (05) :759-767
[7]   Mutations in the APC tumour suppressor gene cause chromosomal instability [J].
Fodde, R ;
Kuipers, J ;
Rosenberg, C ;
Smits, R ;
Kielman, M ;
Gaspar, C ;
van Es, JH ;
Bruekel, C ;
Wiegant, J ;
Giles, RH ;
Clevers, H .
NATURE CELL BIOLOGY, 2001, 3 (04) :433-438
[8]   Hsp-27 expression at diagnosis predicts poor clinical outcome in prostate cancer independent of ETS-gene rearrangement [J].
Foster, C. S. ;
Dodson, A. R. ;
Ambroisine, L. ;
Fisher, G. ;
Moller, H. ;
Clark, J. ;
Attard, G. ;
De-Bono, J. ;
Scardino, P. ;
Reuter, V. E. ;
Cooper, C. S. ;
Berney, D. M. ;
Cuzick, J. .
BRITISH JOURNAL OF CANCER, 2009, 101 (07) :1137-1144
[9]   Genetic and epigenetic alterations in colon cancer [J].
Grady, WM ;
Markowitz, SD .
ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS, 2002, 3 :101-128
[10]   E-cadherin germline mutations in familial gastric cancer [J].
Guilford, P ;
Hopkins, J ;
Harraway, J ;
McLeod, M ;
McLeod, N ;
Harawira, P ;
Taite, H ;
Scoular, R ;
Miller, A ;
Reeve, AE .
NATURE, 1998, 392 (6674) :402-405