The expression of HMGB1 protein and its receptor RAGE in human malignant tumors

被引:117
作者
Kostova, Nora [1 ]
Zlateva, Stanislava [1 ]
Ugrinova, Iva [1 ]
Pasheva, Evdokia [1 ]
机构
[1] Bulgarian Acad Sci, Inst Mol Biol, BU-1113 Sofia, Bulgaria
关键词
HMGB1; protein; Receptor for advanced glycation end products; Carcinoma; Metastasis; GLYCATION END-PRODUCTS; MOBILITY GROUP BOX-1; CHROMATIN PROTEIN; DNA-BINDING; AMPHOTERIN; HMG-1; CELLS; LOCALIZATION; MIGRATION; LIGAND;
D O I
10.1007/s11010-009-0305-0
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
High Mobility Group Box 1 (HMGB1) is a nuclear non-histone protein discovered to be released in the extracellular medium as a response to various stimuli and implicated in cancerogenesis. High HMGB1 levels are reported in a variety of tumor types, but there are few data relating HMGB1 to the histological grade or to a particular cell type and cellular localization. We studied the expression of HMGB1 protein in malignant human tumors of different differentiation level and in tumor metastasis. In all tumor tissues, the protein level is elevated. In moderately differentiated carcinomas, the localization of the protein is perinuclear, while in the low differentiated; there is a tendency for non-specific nuclear localization. HMGB1 protein and its receptor RAGE are identified as a ligand-receptor pair that plays an important role in regulating the invasiveness of tumor cells. RAGE is not produced in all of the tested tumor specimens. We found high level of expression in hepatocellular, colorectal, and breast cribriform carcinomas, but not in malignant testicular specimens. Probably, the RAGE synthesis is related to distinctive tumor types. In metastatic cells, RAGE exhibits higher level of expression losing its specific granular cytosolic pattern characteristic for the primary tumors.
引用
收藏
页码:251 / 258
页数:8
相关论文
共 39 条
  • [1] HMGB proteins and gene expression
    Agresti, A
    Bianchi, ME
    [J]. CURRENT OPINION IN GENETICS & DEVELOPMENT, 2003, 13 (02) : 170 - 178
  • [2] High mobility group 1 protein (HMG-1) stimulates proinflammatory cytokine synthesis in human monocytes
    Andersson, U
    Wang, HC
    Palmblad, K
    Aveberger, AC
    Bloom, O
    Erlandsson-Harris, H
    Janson, A
    Kokkola, R
    Zhang, MH
    Yang, H
    Tracey, KJ
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (04) : 565 - 570
  • [3] Altered expression and localization of creatine kinase B, heterogeneous nuclear ribonucleoprotein F, and high mobility group box 1 protein in the nuclear matrix associated with colon cancer
    Balasubramani, M
    Day, BW
    Schoen, RE
    Getzenberg, RH
    [J]. CANCER RESEARCH, 2006, 66 (02) : 763 - 769
  • [4] Down-regulation of the receptor for advanced glycation end-products (RAGE) supports non-small cell lung carcinoma
    Bartling, B
    Hofmann, HS
    Weigle, B
    Silber, RE
    Simm, A
    [J]. CARCINOGENESIS, 2005, 26 (02) : 293 - 301
  • [5] Upwardly mobile proteins Workshop: The role of HMG proteins in chromatin structure, gene expression and neoplasia
    Bianchi, Marco E.
    Beltrame, Monica
    [J]. EMBO REPORTS, 2000, 1 (02) : 109 - 114
  • [6] SPECIFIC RECOGNITION OF CRUCIFORM DNA BY NUCLEAR-PROTEIN HMG1
    BIANCHI, ME
    BELTRAME, M
    PAONESSA, G
    [J]. SCIENCE, 1989, 243 (4894) : 1056 - 1059
  • [7] BOONYARATANAKOR.V, 1987, MOL CELL BIOL, V18, P4471
  • [8] Revised nomenclature for high mobility group (HMG) chromosomal proteins
    Bustin, M
    [J]. TRENDS IN BIOCHEMICAL SCIENCES, 2001, 26 (03) : 152 - 153
  • [9] DIFFERENTIAL EXPRESSION OF NUCLEAR HMG1, HMG2 PROTEINS AND H1(0) HISTONE IN VARIOUS BLOOD-CELLS
    CABART, P
    KALOUSEK, I
    JANDOVA, D
    HRKAL, Z
    [J]. CELL BIOCHEMISTRY AND FUNCTION, 1995, 13 (02) : 125 - 133
  • [10] Expression profiling of endogenous secretory receptor for advanced glycation end products in human organs
    Cheng, CM
    Tsuneyama, K
    Kominami, R
    Shinohara, H
    Sakurai, S
    Yonekura, H
    Watanabe, T
    Takano, Y
    Yamamoto, H
    Yamamoto, Y
    [J]. MODERN PATHOLOGY, 2005, 18 (10) : 1385 - 1396