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
[31]  
Shibata A, 2001, CANCER EPIDEM BIOMAR, V10, P75
[32]   Sequential observations on the occurrence of preneoplastic and neoplastic lesions in mouse colon treated with azoxymethane and dextran sodium sulfate [J].
Suzuki, R ;
Kohno, H ;
Sugie, S ;
Tanaka, T .
CANCER SCIENCE, 2004, 95 (09) :721-727
[33]   Heat-shock proteins as regulators of apoptosis [J].
Takayama, S ;
Reed, JC ;
Homma, S .
ONCOGENE, 2003, 22 (56) :9041-9047
[34]   Antibodies to heat shock protein 90 in osteosarcoma patients correlate with response to neoadjuvant chemotherapy [J].
Trieb, K ;
Gerth, R ;
Holzer, G ;
Grohs, JG ;
Berger, P ;
Kotz, R .
BRITISH JOURNAL OF CANCER, 2000, 82 (01) :85-87
[35]   Identification of novel genes associated with astrocytoma progression using suppression subtractive hybridization and real-time reverse transcription-polymerase chain reaction [J].
van den Boom, Joerg ;
Wolter, Marietta ;
Blaschke, Britta ;
Knobbe, Christiane B. ;
Reifenberger, Guido .
INTERNATIONAL JOURNAL OF CANCER, 2006, 119 (10) :2330-2338
[36]   Heating the patient: a promising approach? [J].
van der Zee, J .
ANNALS OF ONCOLOGY, 2002, 13 (08) :1173-1184
[37]   PDLIM4 repression by hypermethylation as a potential biomarker for prostate cancer [J].
Vanaja, DK ;
Ballman, KV ;
Morlan, BW ;
Cheville, JC ;
Neumann, RM ;
Lieber, MM ;
Tindall, DJ ;
Young, CYF .
CLINICAL CANCER RESEARCH, 2006, 12 (04) :1128-1136
[38]  
Wang L, 2000, GENE CHROMOSOME CANC, V27, P1, DOI 10.1002/(SICI)1098-2264(200001)27:1<1::AID-GCC1>3.0.CO
[39]  
2-6
[40]   Hsp70 and Hsp90 -: a relay team for protein folding [J].
Wegele, H ;
Müller, L ;
Buchner, J .
REVIEWS OF PHYSIOLOGY, BIOCHEMISTRY AND PHARMACOLOGY, 2004, 151 :1-44