Flow-cytometric DNA analysis and immunohistochemical measurement of Ki-67 and BUdR labeling indices in human brain tumors

1989 ◽  
Vol 70 (3) ◽  
pp. 379-384 ◽  
Author(s):  
Takafumi Nishizaki ◽  
Tetsuji Orita ◽  
Yasuhiro Furutani ◽  
Yukihide Ikeyama ◽  
Hideo Aoki ◽  
...  

✓ Cell proliferation potential was assessed by measuring the labeling indices of the monoclonal antibody Ki-67 and of 5-bromodeoxyuridine (BUdR), and the cellular deoxyribonucleic acid (DNA) content in 48 human brain tumors. The diagnostic and prognostic value of flow-cytometric DNA analysis was also evaluated using ethanol-fixed paraffin-embedded BUdR-labeled specimens; these were the same specimens as were used for measuring the BUdR and Ki-67 labeling indices. Both the Ki-67 and the BUdR labeling indices correlated with the degree of malignancy estimated from conventional histological preparations. The Ki-67 labeling index was 1.7 times greater than the BUdR labeling index. The relationship of DNA aneuploidy to the labeling indices or to morphology in cases of glioma was examined. All of the tumors with an aneuploid line corresponded to malignant glioma classified by histological criteria, although malignant glioma did not always show DNA aneuploidy. In addition, the cases with aneuploid lines showed high BUdR and Ki-67 labeling indices. The cell kinetic data, which indicate the biological character of tumors, allowed prediction of the prognosis of the patients with gliomas. In contrast, despite the presence of an aneuploid line, three of 13 meningiomas showed a benign histological pattern without an aggressive clinical course, and neither the Ki-67 nor the BUdR labeling index was high. These results indicate an unequivocal relationship between DNA aneuploidy and clinical behavior; in general, both labeling indices may prove to be objective indicators of the outcome of patients with brain tumors.

Author(s):  
Ana Maria Tsanaclis ◽  
Françoise Robert ◽  
Jean Michaud ◽  
Steven Brem

ABSTRACT:Brain tumor growth results from the relative proportion of cells contained in three populations: a) cycling/proliferative; b) quiescent (Go)/static, and c) terminally differentiated/dying. The cycling compartment can be detected by the mouse monoclonal Ki-67 antibody, an available, rapid, safe, sensitive, and specific method for immunostaining of proliferative cells. We report the Ki-67 labeling index (LI) in 48 brain tumors. Malignant brain tumors have elevated Lis, ranging from 6.0% to 56.9%: anaplastic astrocytoma, 8.0 ± 7.3; glioblastoma multiforme, 10.1 ±4.2; germinoma, 11.7; medulloblastoma, 13.1 ± 6.6; metastases, 40.3 ± 13.1. By contrast, slow-growing tumors showed lower values (P < .001), approaching 1%: acoustic schwannoma, 0.4 ± 0.6; pituitary adenoma, 1.3 ± 1.9; meningioma, 1.2 ± 1.2; low-grade astrocytoma, < 1; pilocytic astrocytoma, 5.6. Human brain tumors can therefore be ranked according to the percentage of cycling cells with the acoustic schwannoma among the least proliferative and the metastatic carcinoma among the most proliferative. Within a given histotype, the Ki-67 LI may have prognostic and therapeutic implications for the individual patient. Already important for neuro-oncology research, the Ki-67 labeling index should be added to the armamentarium of the clinical neuropathologist to complement the standard histopathologic diagnosis with a cytokinetic analysis of cellular proliferation.


1970 ◽  
Vol 33 (3) ◽  
pp. 281-286 ◽  
Author(s):  
Philippe Benda ◽  
Takesada Mori ◽  
William H. Sweet

✓ Specimens of 16 human brain tumors were studied by the indirect fluorescent-antibody technique to reveal the localization of the particular cerebroprotein found in strikingly increased amounts in human glial tumors as well as in the brain of a patient with Tay-Sachs disease. The cerebro-protein fraction named “10B” by Bogoch was found exclusively in reactive astrocytes, both in astrocytomas and in glioblastomas multiforme. Both the cytoplasm and the cell processes fluoresced upon exposure to antiserum to the “10B” proteins of Tay-Sachs disease. Fluorescence of fibrillary astrocytes located in white matter at some distance from a tumor might be related to discrete edematous changes or constitute an early step in the transition of normal glia to reactive or neoplastic astrocytes. There was no such staining of frankly neoplastic cells or of normal ganglion cells.


1970 ◽  
Vol 33 (2) ◽  
pp. 167-171 ◽  
Author(s):  
Edward R. Laws ◽  
John S. O'Connor

✓ The energy-dependent membrane transport ATPases have been quantitatively determined in 59 human brain tumors and control cerebral cortex. The values for total ATPase were significantly decreased in the 11 types of brain tumors tested, while in the glioma group there was a consistent further decrease in ATPase with increasingly malignant types. The findings suggest that a deficiency in ATPase is a characteristic of neoplasia in the central nervous system.


Author(s):  
Toshiki Yoshimine ◽  
Koji Tokiyoshi ◽  
Motohiko Maruno ◽  
Akira Murasawa ◽  
Hiroyuki Nakata ◽  
...  

1990 ◽  
Vol 73 (3) ◽  
pp. 396-400 ◽  
Author(s):  
Takafumi Nishizaki ◽  
Tetsuji Orita ◽  
Koji Kajiwara ◽  
Norio Ikeda ◽  
Noboru Ohshita ◽  
...  

✓ There are no previous reports correlating the in vitro bromodeoxyuridine (BUdR) labeling index (LI) with the clinical outcome in patients with brain tumors. The reliability of the LI as a predictor of patient survival or recurrence was examined in this study of 66 human brain tumors (19 gliomas, 18 meningiomas, and 29 others). Anti-BUdR staining was performed on surgically extirpated tumor tissue that had been treated with BUdR as previously described. Correlation of the BUdR LI with patient survival or tumor recurrence rate was carried out by the method of Kaplan and Meier. Deoxyribonucleic acid (DNA) aneuploidy was estimated in 52 cases. The results of this study indicate that BUdR LI values correlated well with the clinical course of patients with brain tumor. In comparison with patients with higher LI's, there was both a significantly higher survival rate for tumors other than meningiomas and a higher recurrence-free rate for meningiomas in patients with LI's of less than 4% and 1%, respectively. Although there was a tendency for patients without tumor aneuploidy to show better survival data than the others, no statistical difference was observed. These results suggest that the in vitro BUdR labeling method is reliable for prediction of a patient's prognosis, whereas prognosis on the basis of DNA aneuploidy alone is uncertain.


1987 ◽  
Vol 67 (2) ◽  
pp. 258-262 ◽  
Author(s):  
Raymond Sawaya ◽  
Mario Zuccarello ◽  
Robert Highsmith

✓ This study was undertaken to confirm the presence of alpha-1-antitrypsin (α1-AT) in human brain tumors and to attempt to elucidate its significance. Seventy-seven consecutive unselected patients with various brain tumors were entered in this study. The α1-AT and α2-macroglobulin contents of the tumor extracts were qualitatively assessed by Ouchterlony immunodiffusion techniques. Plasminogen activator (PA) activity was assayed electrophoretically on sodium dodecyl sulfate gels. The patients were divided into two groups according to the positivity of their tumors to α1-AT. Sixty-eight percent of the tumors were positive for α1-AT, and all specimens were negative for α2-macroglobulin. Clinical and biological parameters obtained in all study patients failed to show statistically significant differences between the two groups with the exception of PA activity (p = 0.001), the peritumoral edema as seen on computerized tomography, and the preoperative serum fibrinogen level. These three parameters were higher in the group with specimens positive to α1-AT. This study supports the hypothesis that α1-AT is produced primarily by tumor cells in proportion to the regional proteolytic and inflammatory activity, and may protect the tumor cells.


1987 ◽  
Vol 74 (2) ◽  
pp. 179-182 ◽  
Author(s):  
F. Giangaspero ◽  
C. Doglioni ◽  
M. T. Rivano ◽  
S. Pileri ◽  
J. Gerdes ◽  
...  

1987 ◽  
Vol 67 (3) ◽  
pp. 336-340 ◽  
Author(s):  
Terry Lichtor ◽  
George J. Dohrmann

✓ Glucose utilization in vivo and hexokinase activity and mitochondrial oxygen consumption in vitro were measured in a series of human brain tumors. Several relatively slow-growing tumors appeared to have depressed electron-transport activities coupled with a compensatory elevated glucose utilization. These data suggest that a decrease in oxidative metabolism and a corresponding increase in glycolysis are not necessarily correlated with malignancy in certain human brain tumors.


1979 ◽  
Vol 46 (1-2) ◽  
pp. 39-44 ◽  
Author(s):  
K. Kawamoto ◽  
F. Herz ◽  
R. C. Wolley ◽  
A. Hirano ◽  
H. Kajikawa ◽  
...  

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