Distinctive Expression and Function of Four GSDM Family Genes (GSDMA-D) in Normal and Malignant Upper Gastrointestinal Epithelium

被引:218
作者
Saeki, Norihisa [1 ]
Usui, Takebumi [1 ,2 ]
Aoyagi, Kazuhiko [1 ]
Kim, Dal Ho [1 ,2 ]
Sato, Megumi [1 ]
Mabuchi, Tomoko [1 ]
Yanagihara, Kazuyoshi [3 ]
Ogawa, Kenji [2 ]
Sakamoto, Hiromi [1 ]
Yoshida, Teruhiko [1 ]
Sasaki, Hiroki [1 ]
机构
[1] Natl Canc Ctr, Div Genet, Tokyo 1040045, Japan
[2] Tokyo Womens Med Univ, Sch Med, Med Ctr E, Tokyo, Japan
[3] Natl Canc Ctr, Cent Anim Lab, Tokyo, Japan
关键词
SQUAMOUS-CELL CARCINOMAS; TUMOR-SUPPRESSOR GENE; HUMAN GASTRIC-CANCER; MOUSE-CHROMOSOME; 11; NUDE-MICE; AMPLIFICATION; C-ERBB-2; DNA; IDENTIFICATION; ESTABLISHMENT;
D O I
10.1002/gcc.20636
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Gasdermin (GSDM or GSDMA), expressed in the upper gastrointestinal tract but frequently silenced in gastric cancers (GCs), regulates apoptosis of the gastric epithelium. It has three human homologs, GSDMB, GSDMC, and GSDMD (GSDM family) and they are considered to be involved in the regulation of epithelial apoptosis but not yet known. We investigated the expression pattern of the family genes in the upper gastrointestinal epithelium and cancers. Reverse transcriptase-polymerase chain reaction revealed that, unlike GSDMA expressed in differentiated cells, GSDMB is expressed in proliferating cells and GSDMD in differentiating cells. GSDMC, meanwhile, is expressed in both differentiating and differentiated cells. Colony formation assay showed that GSDMB, closely related to GSDMA, has no cell-growth inhibition activity in gastric cancer cells, and that GSDMC and GSDMD, respectively, exhibit the activity with different strengths from that of GSDMA. Expression analyses of the four family genes in esophageal and GCs suggested that GSDMC and GSDMD as well as GSDMA are tumor suppressors and that GSDMB, which was amplified and overexpressed in some GCs, could be an oncogene. The results of the expression analysis and colony formation assay suggest that each family gene may have a distinct function in the upper gastrointestinal epithelium. (c) 2008 Wiley-Liss, Inc.
引用
收藏
页码:261 / 271
页数:11
相关论文
共 44 条
  • [31] A new mutation Rim3 resembling Reden is mapped close to retinoic acid receptor alpha (Rara) gene on mouse Chromosome 11
    Sato, H
    Koide, T
    Masuya, H
    Wakana, S
    Sagai, T
    Umezawa, A
    Ishiguro, S
    Tama, M
    Shiroishi, T
    [J]. MAMMALIAN GENOME, 1998, 9 (01) : 20 - 25
  • [32] SEKIGUCHI M, 1978, JPN J EXP MED, V48, P61
  • [33] Sekiguchi M., 1994, ATLAS HUMAN TUMOR CE, P287
  • [34] THE SH2 DOMAIN PROTEIN GRB-7 IS CO-AMPLIFIED, OVEREXPRESSED AND IN A TIGHT COMPLEX WITH HER2 IN BREAST-CANCER
    STEIN, D
    WU, J
    FUQUA, SAW
    ROONPRAPUNT, C
    YAJNIK, V
    DEUSTACHIO, P
    MOSKOW, JJ
    BUCHBERG, AM
    OSBORNE, CK
    MARGOLIS, B
    [J]. EMBO JOURNAL, 1994, 13 (06) : 1331 - 1340
  • [35] Takubo K, 2007, PATHOLOGY ESOPHAGUS, P8
  • [36] Members of a novel gene family, Gsdm, are expressed exclusively in the epithelium of the skin and gastrointestinal tract in a highly tissue-specific manner
    Tamura, Masaru
    Tanaka, Shigekazu
    Fujii, Tomoaki
    Aoki, Aya
    Komiyama, Hiromitu
    Ezawa, Kiyoshi
    Sumiyama, Kenta
    Sagai, Tomoko
    Shiroishi, Toshibiko
    [J]. GENOMICS, 2007, 89 (05) : 618 - 629
  • [37] Caspase 8 is deleted or silenced preferentially in childhood neuroblastomas with amplification of MYCN
    Teitz, T
    Wei, T
    Valentine, MB
    Vanin, EF
    Grenet, J
    Valentine, VA
    Behm, FG
    Look, AT
    Lahti, JM
    Kidd, VJ
    [J]. NATURE MEDICINE, 2000, 6 (05) : 529 - 535
  • [38] Structure, expression and chromosome mapping of MLZE, a novel gene which is preferentially expressed in metastatic melanoma cells
    Watabe, E
    Ito, A
    Asada, H
    Endo, Y
    Kobayashi, T
    Nakamoto, K
    Itami, S
    Takao, S
    Shinomura, Y
    Aikou, T
    Yoshikawa, K
    Matsuzawa, Y
    Kitamura, Y
    Nojima, H
    [J]. JAPANESE JOURNAL OF CANCER RESEARCH, 2001, 92 (02): : 140 - 151
  • [39] Down-regulation of caveolin-1, a candidate tumor suppressor gene, in sarcomas
    Wiechen, K
    Sers, C
    Agoulnik, A
    Arlt, K
    Dietel, M
    Schlag, PM
    Schneider, U
    [J]. AMERICAN JOURNAL OF PATHOLOGY, 2001, 158 (03) : 833 - 839
  • [40] WOLHER R, 1991, J CLIN PATHOL, V96, P243