Nitric oxide induces oral squamous cell carcinoma cells apoptosis with p53 accumulation

被引:31
作者
Zhao, SF [1 ]
Tong, XY [1 ]
Zhu, FD [1 ]
机构
[1] Zhejiang Univ, Sch Stomatol, Dept Oral & Maxillofacial Surg, Hangzhou 310006, Peoples R China
关键词
nitric oxide; tongue; squamous cell carcinoma; apoptosis; p53;
D O I
10.1016/j.oraloncology.2005.04.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Nitric oxide has been reported to have cytotoxic effects in several tumor cells. The objective of this study was to investigate the effects of exogenous nitric oxide on apopotosis in oral squarrous cell carcinoma cells and to reveal its possible mechanism. Tca8113 cells were cultured with various concentrations of nitric oxide that were released from sodium nitroprusside (SNP). Nitrite/nitrate levels in the culture supernatant were determined using a commercial available nitric oxide kit. Cellular proliferation was determined by MTT assay. Apoptosis was detected by flow cytometry. Expression of inducible nitric oxide synthase (iNOS) was determined by immunocytochemistry. p53 expression was assessed by Western blot. SNP can release nitric oxide into the culture medium in a dose-dependent manner. Nitric oxide remarkably inhibits proliferation in a dose and time-dependent manners and Lead to apoptosis of the Tca8113 cell. The p53 expression was elevated accompanying by the increased apoptotic cells. No difference of iNOS was found whether or not the cells were treated with SNP. Exogenous nitric oxide had an inhibitory effect on Tca8113 cells proliferation in a dose and time-dependent manners and possibly via p53 dependent apoptosis pathway. Exogenous nitric oxide had no significant effect on cellular iNOS protein. (C) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:785 / 790
页数:6
相关论文
共 31 条
  • [1] P53 CONTROLS BOTH THE G(2)/M AND THE G(1) CELL-CYCLE CHECKPOINTS AND MEDIATES REVERSIBLE GROWTH ARREST IN HUMAN FIBROBLASTS
    AGARWAL, ML
    AGARWAL, A
    TAYLOR, WR
    STARK, GR
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (18) : 8493 - 8497
  • [2] Role of nitric oxide in mediation of macrophage cytotoxicity and apoptosis
    Albina, JE
    Reichner, JS
    [J]. CANCER AND METASTASIS REVIEWS, 1998, 17 (01) : 39 - 53
  • [3] FEEDBACK INHIBITION OF NITRIC-OXIDE SYNTHASE ACTIVITY BY NITRIC-OXIDE
    ASSREUY, J
    CUNHA, FQ
    LIEW, FY
    MONCADA, S
    [J]. BRITISH JOURNAL OF PHARMACOLOGY, 1993, 108 (03) : 833 - 837
  • [4] Multiple roles of the tumor suppressor p53
    Bargonetti, J
    Manfredi, JJ
    [J]. CURRENT OPINION IN ONCOLOGY, 2002, 14 (01) : 86 - 91
  • [5] Nitric oxide and the immune response
    Bogdan, C
    [J]. NATURE IMMUNOLOGY, 2001, 2 (10) : 907 - 916
  • [6] CANCER STATISTICS, 1994
    BORING, CC
    SQUIRES, TS
    TONG, T
    MONTGOMERY, S
    [J]. CA-A CANCER JOURNAL FOR CLINICIANS, 1994, 44 (01) : 7 - 26
  • [7] Correlation between type II nitric oxide synthase and p53 expression in oral squamous cell carcinoma
    Brennan, PA
    Palacios-Callender, M
    Umar, T
    Hughes, D
    Spedding, AV
    Zaki, GA
    Langdon, JD
    [J]. BRITISH JOURNAL OF ORAL & MAXILLOFACIAL SURGERY, 2000, 38 (06) : 627 - 632
  • [8] p53 accumulation in apoptotic macrophages is an energy demanding process that precedes cytochrome c release in response to nitric oxide
    Brockhaus, F
    Brüne, B
    [J]. ONCOGENE, 1999, 18 (47) : 6403 - 6410
  • [9] Nitric oxide (NO):: an effector of apoptosis
    Brüne, B
    von Knethen, A
    Sandau, KB
    [J]. CELL DEATH AND DIFFERENTIATION, 1999, 6 (10) : 969 - 975
  • [10] Chao Jui-I, 2004, Carcinogenesis, V25, P645