免疫组织化学
原发性中枢神经系统淋巴瘤
病理
生物
中枢神经系统
中心体
细胞
医学
细胞周期
神经科学
遗传学
作者
Kotaro Matsuda,Yasuo Sugita,Takuya Furuta,Mayuko Moritsubo,Koichi Ohshima,Motohiro Morioka,Kenji Takahashi,Koichi Higaki,Akiyoshi Kakita
摘要
Abstract Transforming acidic coiled‐coil‐containing protein 3 (TACC3) plays an important role in centrosome/microtubule dynamics. Deregulation of centrosomes/microtubules causes mitotic spindle defects, leading to tumorigenesis. However, the correlation between TACC3 and primary central nervous system lymphomas (PCNSLs) is unknown. The present study investigated the association between the immunohistochemical expression of TACC3, p53, and Ki‐67, and the clinical factors in 40 PCNSLs. We evaluated the staining of TACC3 based on the histoscore (H‐score) that contains a semiquantitative evaluation of both the intensity of staining, and the percentage of positive cells. Expression level of each component was classified as low or high according to the median H‐score value. Patients with PCNSLs were divided into groups depending on TACC3 expression levels (no expression and low expression, 18; high expression, 22). Disease‐free survival and overall survival of patients with high TACC3 expression were significantly shorter ( p < 0.01 and p < 0.05, respectively). These results suggest that elevated expression of TACC3 could reflects aggressiveness of primary central nervous system lymphomas.
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