Eur Rev Med Pharmacol Sci 2014; 18 (4): 516-519

Expression of CyclinD1 and Ki-67 proteins in gliomas and its clinical significance

D.-W. Qu, H.-S. Xu, X.-J. Han, Y.-L. Wang, C.-J. Ouyang

Department of Neurobiology and Anatomy, Xuzhou Medical College, Xuzhou, China. xhs51@126.com


OBJECTIVES: To investigate the expression of cyclinD1 and Ki-67 proteins in gliomas and its significance.

PATIENTS AND METHODS: The immunohistochemistry was used to detect the expression of cyclinD1 and Ki-67 proteins in 18 cases of normal brain tissues, 32 cases of low-grade gliomas, and 24 cases of high-grade gliomas.

RESULTS: The cyclinD1 positive ratio in normal brain tissues, low-grade gliomas, and high-grade gliomas were 4/18, 15/32, and 18/24, respectively, with statistically significant difference (p < 0.05). Differences were significant by pairwise comparison between normal brain tissue with high-grade gliomas and low-grade gliomas with high-grade glioma groups (p < 0.01). However, there was no significant differences between normal brain tissue with low-grade gliomas. The Ki-67 positive ratio in normal brain tissues, low-grade gliomas, and high-grade gliomas were 5/18, 21/32, and 20/24, respectively. The difference among three tissues was statistically significant (p < 0.05). Differences were significant by pairwise comparison between normal brain tissue with low-grade gliomas and normal brain tissue with high-grade glioma group (p < 0.01). There is no difference between low-grade gliomas and high-grade gliomas (p > 0.05). Spearman’s rank correlation confirmed that cyclinD1 and Ki-67 was positively correlated in low-grade gliomas and high-level brain tumor (p < 0.05), but no correlation in the normal brain tissue (p > 0.05).

CONCLUSIONS: The expression of CyclinD1 and Ki-67 increased in gliomas, suggesting that both may play an important role in the occurrence of gliomas.

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To cite this article

D.-W. Qu, H.-S. Xu, X.-J. Han, Y.-L. Wang, C.-J. Ouyang
Expression of CyclinD1 and Ki-67 proteins in gliomas and its clinical significance

Eur Rev Med Pharmacol Sci
Year: 2014
Vol. 18 - N. 4
Pages: 516-519