How is the mutational status for tumor suppressors p53 and p16INK4A in MFH of the bone?

被引:8
|
作者
Taubert, H
Berger, D
Hinze, R
Meye, A
Würl, P
Hogendoorn, PCW
Holzhausen, HJ
Schmidt, H
Rath, FW
机构
[1] Univ Halle Wittenberg, Inst Pathol, D-06097 Halle, Germany
[2] Univ Halle Wittenberg, Ctr Basic Med Res, D-06097 Halle, Germany
[3] Univ Halle Wittenberg, Clin Gen Surg, D-06097 Halle, Germany
[4] Acad Hosp Leiden, Dept Pathol, NL-2300 RC Leiden, Netherlands
关键词
malignant fibrous histiocytoma of the bone; p53; p16; tumor suppressor genes; mutational analysis;
D O I
10.1016/S0304-3835(97)00423-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Both tumor suppressor genes p53 and p16(INK4A) play a crucial role in the control of cell cycle and tumor development. In this study 19 malignant fibrous histiocytomas of the bone (MFH-b), a very rare sarcoma entity, were investigated for mutations in p53 and p16 genes by a PCR-SSCP-sequencing analysis. In the tumor samples two p53 mutations and two polymorphisms (one in the p53 gene and one in the p16 gene) were found. The occurrence rate for p53 mutations and the absence of p16 mutations in MFH-b are comparable to the findings for MFH of soft tissues (MFH-st) and osteosarcomas, suggesting that p53 rather than p16 may play a role in tumorigenesis of MFH-b. (C) 1998 Elsevier Science Ireland Ltd.
引用
收藏
页码:147 / 151
页数:5
相关论文
共 50 条
  • [21] A senescence program controlled by p53 and p16INK4a contributes to the outcome of cancer therapy
    Schmitt, CA
    Fridman, JS
    Yang, M
    Lee, S
    Baranov, E
    Hoffman, RM
    Lowe, SW
    CELL, 2002, 109 (03) : 335 - 346
  • [22] Clinical significance of p16INK4A and p53 overexpression in endocrine tumors of the gastrointestinal tract
    Li, Anna Fen-Yau
    Tsay, Shyh-Haw
    Liang, Wen-Yih
    Li, Wing-Yin
    Chen, Jeou-Yuan
    AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2006, 126 (06) : 856 - 865
  • [23] The tumor suppressor protein p16INK4a
    Serrano, M
    EXPERIMENTAL CELL RESEARCH, 1997, 237 (01) : 7 - 13
  • [24] VentX trans-Activates p53 and p16ink4a to Regulate Cellular Senescence
    Wu, Xiaoming
    Gao, Hong
    Ke, Weixiong
    Hager, Martin
    Xiao, Sheng
    Freeman, Michael R.
    Zhu, Zhenglun
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (14) : 12693 - 12701
  • [25] Human papilloma virus (HPV) status, p16INK4a, and p53 overexpression in epithelial malignant and borderline ovarian neoplasms
    Giordano, Glovanna
    Azzoni, Cinzia
    D'Adda, Tiziana
    Rocca, Alba
    Gnetti, Letizia
    Frolo, Elisabetta
    Merislo, Carla
    Melpignano, Mauro
    PATHOLOGY RESEARCH AND PRACTICE, 2008, 204 (03) : 163 - 174
  • [26] Mutations of the INK4A-arf and p53 tumor suppressors genes in genital carcinoma
    Soufir, N
    Vilmer, C
    Thibaudeau, O
    Bachevalier, F
    Deslestaing, G
    Cavelier-Balloy, B
    Basset-Séguin, N
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2001, 117 (03) : 777 - 777
  • [27] Real-time in vivo imaging of p16Ink4a reveals cross talk with p53
    Yamakoshi, Kimi
    Takahashi, Akiko
    Hirota, Fumiko
    Nakayama, Rika
    Ishimaru, Naozumi
    Kubo, Yoshiaki
    Mann, David J.
    Ohmura, Masako
    Hirao, Atsushi
    Saya, Hideyuki
    Arase, Seiji
    Hayashi, Yoshio
    Nakao, Kazuki
    Matsumoto, Mitsuru
    Ohtani, Naoko
    Hara, Eiji
    JOURNAL OF CELL BIOLOGY, 2009, 186 (03): : 393 - 407
  • [28] Dioxin-induced immortalization of normal human keratinocytes and silencing of p53 and p16INK4a
    Ray, SS
    Swanson, HI
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (26) : 27187 - 27193
  • [29] Expression of P16INK4a, p53 AND COX-2 in colorectal carcinoma and their clinical significance
    Abdennadher, I. Miladi
    Ayadi, L.
    Khabir, A.
    Frikha, F.
    Kallel, L.
    Makni, S.
    Frikha, M.
    Gargouri, A.
    Gargouri, R.
    Boudawara, T. Sellami
    HISTOPATHOLOGY, 2008, 53 : 149 - 149
  • [30] The inherent instability of mutant p53 is alleviated by Mdm2 or p16INK4a loss
    Terzian, Tamara
    Suh, Young-Ah
    Iwakuma, Tomoo
    Post, Sean M.
    Neumann, Manja
    Lang, Gene A.
    Van Pelt, Carolyn S.
    Lozano, Guillermina
    GENES & DEVELOPMENT, 2008, 22 (10) : 1337 - 1344