Absence of mutations in the transforming growth factor-β inducible early gene 1, TIEG1, in pancreatic cancer

被引:10
作者
Antonello, D
Moore, PS
Zamboni, G
Falconi, M
Scarpa, A
机构
[1] Univ Verona, Dept Pathol, I-37134 Verona, Italy
[2] Univ Verona, Dept Surg, I-37134 Verona, Italy
关键词
pancreas; cancer; apoptosis; TIEG1; transforming growth factor beta;
D O I
10.1016/S0304-3835(01)00802-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Pancreatic cancers frequently have defects in components of the transforming growth factor-beta (TGF-beta) signaling pathway. TIEG1 (TGF-beta inducible early gene) is a recently characterized transcription factor regulated by TGF-beta that induces apoptosis when overexpressed in pancreatic adenocarcinoma cell lines. Alterations on chromosome 8q, where TIEG1 is located, are also relatively frequent in pancreatic cancers. To determine if TIEG1 may be involved in the tumorigenesis of pancreatic cancer, we performed mutational screening of this gene in 22 pancreatic cancer cell lines. No sequence alterations were observed. Reverse transcription-polymerase chain reaction analysis was also performed to rule out the possibility that the expression of the gene is altered by genetic events other than mutation. Likewise, no alterations in expression were found. Thus, an essential role of TIEG1 in pancreatic cancer can be excluded. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:179 / 183
页数:5
相关论文
共 27 条
  • [1] Achille A, 1996, CANCER RES, V56, P3808
  • [2] KARYOTYPIC ABNORMALITIES IN TUMORS OF THE PANCREAS
    BARDI, G
    JOHANSSON, B
    PANDIS, N
    MANDAHL, N
    BAKJENSEN, E
    ANDRENSANDBERG, A
    MITELMAN, F
    HEIM, S
    [J]. BRITISH JOURNAL OF CANCER, 1993, 67 (05) : 1106 - 1112
  • [3] A zinc-finger transcription factor induced by TGF-β promotes apoptotic cell death in epithelial Mv1Lu cells
    Chalaux, E
    López-Rovira, T
    Rosa, JL
    Pons, G
    Boxer, LM
    Bartrons, R
    Ventura, F
    [J]. FEBS LETTERS, 1999, 457 (03) : 478 - 482
  • [4] Three conserved transcriptional repressor domains are a defining feature of the TIEG subfamily of Sp1-like zinc finger proteins
    Cook, T
    Gebelein, B
    Belal, M
    Mesa, K
    Urrutia, P
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (41) : 29500 - 29504
  • [5] TIEG proteins join the Smads as TGF-β-regulated transcription factors that control pancreatic cell growth
    Cook, T
    Urrutia, R
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2000, 278 (04): : G513 - G521
  • [6] Molecular cloning and characterization of TIEG2 reveals a new subfamily of transforming growth factor-β-inducible Sp1-like zinc finger-encoding genes involved in the regulation of cell growth
    Cook, T
    Gebelein, B
    Mesa, K
    Mladek, A
    Urrutia, R
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (40) : 25929 - 25936
  • [7] TGFβ-inducible early gene (TIEG) also codes for early growth response α (EGRα):: Evidence of multiple transcripts from alternate promoters
    Fautsch, MP
    Vrabel, A
    Subramaniam, M
    Hefferen, TE
    Spelsberg, TC
    Wieben, ED
    [J]. GENOMICS, 1998, 51 (03) : 408 - 416
  • [8] Goggins M, 1998, CANCER RES, V58, P5329
  • [9] A set of proteins interacting with transcription factor Sp1 identified in a two-hybrid screening
    Gunther, M
    Laithier, M
    Brison, O
    [J]. MOLECULAR AND CELLULAR BIOCHEMISTRY, 2000, 210 (1-2) : 131 - 142
  • [10] DPC4, a candidate tumor suppressor gene at human chromosome 18q21.1
    Hahn, SA
    Schutte, M
    Hoque, ATMS
    Moskaluk, CA
    daCosta, LT
    Rozenblum, E
    Weinstein, CL
    Fischer, A
    Yeo, CJ
    Hruban, RH
    Kern, SE
    [J]. SCIENCE, 1996, 271 (5247) : 350 - 353