Locomotion and proliferation of glioblastoma cells in vitro:: statistical evaluation of videomicroscopic observations

被引:53
作者
Hegedüs, B
Czirók, A
Fazekas, I
Bábel, T
Madarász, E
Vicsek, T
机构
[1] Eotvos Lorand Univ, Dept Biol Phys, H-1117 Budapest, Hungary
[2] Natl Inst Neurosurg, Budapest, Hungary
[3] Hungarian Acad Sci, Inst Expt Med, Budapest, Hungary
关键词
glioblastoma multiforme; videomicroscopy; cell motility; proliferation;
D O I
10.3171/jns.2000.92.3.0428
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Object. The motility and doubling of human glioblastoma cells were investigated by means of statistical evaluation of large sets of data obtained using computer-aided videomicroscopy. Methods. Data were obtained on cells in four established glioblastoma cell lines and also on primary tumor cells cultured from fresh surgical samples. Growth rates and cell cycle times were measured in individual microscopic fields. The averages of cell cycle time and the duplication time for the recorded cell populations were 26.2 +/- 5.6 hours and 38 +/- 4 hours, respectively. With these parameters, no significant differences among the cell lines were revealed. Also, there was no correlation in the cell cycle time of a parent cell and its progeny in any of the cultures. Statistical analysis of cell locomotion revealed an exponential distribution of cell velocities and strong fluctuations in individual cell velocities across rime. The average velocity values ranged from 4.2 to 27.9 mu m/hour. In spite of the uniform histopathological classification of the four tumors, each cell line produced by these tumors displayed distinct velocity distribution profiles and characteristic average velocity values. A comparison of recently established primary cultures with cell lines that had propagated multiple times indicated that cells derived from different tumors sustain their characteristic locomotor activity after several passages. Conclusions. It can be inferred from the data that statistical evaluation of physical parameters of cell locomotion can provide additional tools for tumor diagnosis.
引用
收藏
页码:428 / 434
页数:7
相关论文
共 25 条
[1]   HUMAN-MALIGNANT ASTROCYTOMA XENOGRAFTS MIGRATE IN RAT-BRAIN - A MODEL FOR CENTRAL NERVOUS-SYSTEM CANCER-RESEARCH [J].
BERNSTEIN, JJ ;
GOLDBERG, WJ ;
LAWS, ER .
JOURNAL OF NEUROSCIENCE RESEARCH, 1989, 22 (02) :134-143
[2]   HETEROGENEITY OF GENOTYPIC AND PHENOTYPIC CHARACTERISTICS OF 15 PERMANENT CELL-LINES DERIVED FROM HUMAN GLIOMAS [J].
BIGNER, DD ;
BIGNER, SH ;
PONTEN, J ;
WESTERMARK, B ;
MAHALEY, MS ;
RUOSLAHTI, E ;
HERSCHMAN, H ;
ENG, LF ;
WIKSTRAND, CJ .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1981, 40 (03) :201-229
[3]   MEASURES OF TUMOR PROLIFERATIVE ACTIVITY [J].
BROOKS, DJ ;
GAREWAL, HS .
INTERNATIONAL JOURNAL OF CLINICAL & LABORATORY RESEARCH, 1992, 22 (04) :196-200
[4]   Mutations of mitotic checkpoint genes in human cancers [J].
Cahill, DP ;
Lengauer, C ;
Yu, J ;
Riggins, GJ ;
Willson, JKV ;
Markowitz, SD ;
Kinzler, KW ;
Vogelstein, B .
NATURE, 1998, 392 (6673) :300-303
[5]   Mitogens as motogens [J].
Chicoine, MR ;
Silbergeld, DL .
JOURNAL OF NEURO-ONCOLOGY, 1997, 35 (03) :249-257
[6]  
CHICOINE MR, 1995, CANCER, V75, P2904, DOI 10.1002/1097-0142(19950615)75:12<2904::AID-CNCR2820751218>3.0.CO
[7]  
2-2
[8]   ASSESSMENT OF BRAIN-TUMOR CELL MOTILITY IN-VIVO AND IN-VITRO [J].
CHICOINE, MR ;
SILBERGELD, DL .
JOURNAL OF NEUROSURGERY, 1995, 82 (04) :615-622
[9]   Exponential distribution of locomotion activity in cell cultures [J].
Czirok, A ;
Schlett, K ;
Madarasz, E ;
Vicsek, T .
PHYSICAL REVIEW LETTERS, 1998, 81 (14) :3038-3041
[10]   DETERMINATION OF THE PROLIFERATIVE POTENTIAL OF HUMAN-BRAIN TUMORS USING THE MONOCLONAL-ANTIBODY KI-67 [J].
DECKERT, M ;
REIFENBERGER, G ;
WECHSLER, W .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 1989, 115 (02) :179-188