Prognostic significance of S-phase fractions in peritumoral invading zone analyzed by laser scanning cytometry in patients with high-grade glioma: A preliminary study

被引:1
|
作者
Nakajima, Syoichi [1 ,2 ]
Morii, Ken [1 ]
Takahashi, Hitoshi [3 ]
Fujii, Yukihiko [1 ]
Yamanaka, Ryuya [4 ]
机构
[1] Niigata Univ, Brain Res Inst, Dept Neurosurg, Niigata 9518585, Japan
[2] Niigata Neurosurg Hosp, Dept Neurosurg, Niigata 9501101, Japan
[3] Niigata Univ, Brain Res Inst, Dept Pathol, Niigata 9518585, Japan
[4] Kyoto Prefectural Univ Med, Grad Sch Med Sci, Lab Mol Target Therapy Canc, 465 Kajii Cho, Kyoto 6028566, Japan
关键词
cell cycle; high grade glioma; invading zone; S phase; laser scanning cytometry; prognostic significance; FLOW-CYTOMETRY; DNA-PLOIDY; CELL-CYCLE; CANCER; INDEX; EXPRESSION; RELEVANCE; TISSUE; GENE;
D O I
10.3892/ol.2016.4205
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The predominant characteristic of malignant glioma is the presence of invading tumor cells in the peritumoral zone. Distinguishing between tumor cells and normal cells in a peritumoral lesion is challenging. Therefore, the aim of the present study was to investigate the cell-cycle phase measurements of fixed paraffin-embedded specimens from the peritumoral invading zone of high-grade gliomas using laser scanning cytometry. A total of 12 high-grade gliomas (2 anaplastic astrocytomas and 10 glioblastomas) were studied. The tumor core and peritumoral invading zone of each tumor specimen were investigated. Tissue sections (50 mu m) from the paraffin blocks were deparaffinized, rehydrated and enzymatically disintegrated, and the cells in suspension were stained with propidium iodide and placed on microscope slides. A slight trend for an increased S-phase fraction in the peritumoral invading zone compared with the tumor core was observed (P=0.24). Additionally, there was a trend for a decrease in the overall survival time of patients with increasing peritumoral invading zone S-phase fraction (P=0.12). These data suggest that laser scanning cytometry is a powerful and clinically relevant tool for the objective analysis of the cell cycle in malignant gliomas.
引用
收藏
页码:2106 / 2110
页数:5
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