Three-dimensional cell organization leads to a different type of ionizing radiation-induced cell death: MG-63 monolayer cells undergo mitotic catastrophe while spheroids die of apoptosis

被引:0
作者
Indovina, Paola
Rainaldi, Gabriella
Santini, Maria Teresa
机构
[1] Ist Super Sanita, Dipartimento Ematol Oncol & Med Mol, I-00161 Rome, Italy
[2] Complesso Univ Monte S Angelo, CNR, INFM, I-80126 Naples, Italy
关键词
three-dimensional tumor spheroid; mitotic catastrophe; apoptosis; ionizing radiation;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The type of cell death occurring in the same cell line (MG-63 human osteosarcoma cells) grown in monolayer or as three-dimensional spheroids after exposure to 5 Gy of ionizing radiation was determined. Morphological analyses using the chromatin dye Hoechst 33258 demonstrated that spheroids showed the typical characteristics of apoptosis, while monolayer cells revealed those typical of mitotic catastrophe. In order to better characterize these two types of cell death, the role of caspases was examined in irradiated monolayer cells and spheroids using the broad spectrum caspase inhibitor zVAD-fmk. Death in monolayer cells was caspase-independent, whereas spheroid death was characterized by caspase dependence. Members of the Bcl-2 family of proteins and survivin involved in cell death processes were also studied by Western blot analysis. The pro-apoptotic protein Bax increased in spheroids, whereas this protein remained unchanged in monolayer cells after the same 5-Gy irradiation. The antiapoptotic protein Bcl-2, on the other hand, remained unchanged in both monolayer cells and spheroids. Finally, survivin increased significantly after irradiation in both cells in monolayer and spheroids. The results presented suggest that three-dimensional cell organization leads to a different type of cell death after exposure to ionizing radiation. Thus, the use of spheroids, a cell model which mimics in vivo solid tumors more closely than cells grown in monolayer, is more appropriate when, investigating the effects of antineoplastic treatments such as ionizing radiation.
引用
收藏
页码:1473 / 1483
页数:11
相关论文
共 49 条
  • [1] Reasons to reconsider the significance of apoptosis for cancer therapy
    Abend, M
    [J]. INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 2003, 79 (12) : 927 - 941
  • [2] Survivin and apoptosis control
    Altieri, DC
    [J]. ADVANCES IN CANCER RESEARCH, VOL 88, 2003, 88 : 31 - 52
  • [3] Apoptosis - The cell's silent exit
    Bar, PR
    [J]. LIFE SCIENCES, 1996, 59 (5-6) : 369 - 378
  • [4] Benderitter M, 2003, RADIAT RES, V159, P471, DOI 10.1667/0033-7587(2003)159[0471:TCMAAB]2.0.CO
  • [5] 2
  • [6] Role of HIF-1α or in hypoxia-mediated apoptosis, cell proliferation and tumour angiogenesis
    Carmeliet, P
    Dor, Y
    Herbert, JM
    Fukumura, D
    Brusselmans, K
    Dewerchin, M
    Neeman, M
    Bono, F
    Abramovitch, R
    Maxwell, P
    Koch, CJ
    Ratcliffe, P
    Moons, L
    Jain, RK
    Collen, D
    Keshet, E
    [J]. NATURE, 1998, 394 (6692) : 485 - 490
  • [7] Mitotic catastrophe constitutes a special case of apoptosis whose suppression entails aneuploidy
    Castedo, M
    Perfettini, JL
    Roumier, T
    Valent, A
    Raslova, H
    Yakushijin, K
    Horne, D
    Feunteun, J
    Lenoir, G
    Medema, R
    Vainchenker, W
    Kroemer, G
    [J]. ONCOGENE, 2004, 23 (25) : 4362 - 4370
  • [8] Cell death by mitotic catastrophe: a molecular definition
    Castedo, M
    Perfettini, JL
    Roumie, T
    Andreau, K
    Medema, R
    Kroemer, G
    [J]. ONCOGENE, 2004, 23 (16) : 2825 - 2837
  • [9] Survivin enhances radiation resistance in primary human glioblastoma cells via caspase-independent mechanisms
    Chakravarti, A
    Zhai, GG
    Zhang, M
    Malhotra, R
    Latham, DE
    Delaney, MA
    Robe, P
    Nestler, U
    Song, QH
    Loeffler, J
    [J]. ONCOGENE, 2004, 23 (45) : 7494 - 7506
  • [10] Control of mitochondrial integrity by Bcl-2 family members and caspase-independent cell death
    Donovan, M
    Cotter, TG
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2004, 1644 (2-3): : 133 - 147