Deckert-Schlüter M, Rang A, Wiestler O D
Institut für Neuropathologie, Universitätskliniken Bonn, Germany.
Acta Neuropathol. 1998 Aug;96(2):157-62. doi: 10.1007/s004010050876.
The incidence of primary lymphomas of the central nervous system (CNS) has significantly increased over the last years. However, the pathogenesis of this serious and fatal disease is still largely unknown. The aim of the present study was to investigate whether impairment of apoptosis is involved in the pathogenesis of primary CNS lymphomas. A series of 35 primary CNS lymphomas was investigated for the presence of apoptotic cells and the expression of apoptosis-inhibiting and proapoptotic gene products of the bcl family by application of the terminal deoxynucleotidyl transferase-mediated dUTP-nick end labeling (TUNEL) technique and immunohistochemistry. The majority (23/35) of the tumors contained no or less than 10% of apoptotic cells. All tumors were MIB-1 positive, and 53% of them showed a high proliferative activity with more than 20% MIB-1-positive cells. The bcl-2 gene was expressed in 54% of the tumors (19/35), whereas bcl-x and bax gene products were present in only a low fraction of these lymphomas (4/35). In contrast, bak and the tumor suppressor gene p53 product were not detectable. These findings indicate that apoptosis is inhibited in the majority of this series of primary CNS lymphomas. Since there was no statistical correlation between the degree of apoptosis and the expression of proteins of the bcl gene family, other apoptosis-inhibiting factors may be involved in the pathogenesis of primary CNS lymphomas.
在过去几年中,中枢神经系统(CNS)原发性淋巴瘤的发病率显著上升。然而,这种严重致命疾病的发病机制仍 largely unknown。本研究的目的是调查凋亡受损是否参与原发性中枢神经系统淋巴瘤的发病机制。通过应用末端脱氧核苷酸转移酶介导的dUTP缺口末端标记(TUNEL)技术和免疫组织化学,对35例原发性中枢神经系统淋巴瘤进行了一系列研究,以检测凋亡细胞的存在以及bcl家族凋亡抑制和促凋亡基因产物的表达。大多数(23/35)肿瘤中凋亡细胞数量为零或少于10%。所有肿瘤MIB-1均呈阳性,其中53%表现出高增殖活性,MIB-1阳性细胞超过20%。54%的肿瘤(19/35)表达bcl-2基因,而bcl-x和bax基因产物仅在一小部分这些淋巴瘤中存在(4/35)。相比之下,bak和肿瘤抑制基因p53产物无法检测到。这些发现表明,在这一系列原发性中枢神经系统淋巴瘤中,大多数凋亡受到抑制。由于凋亡程度与bcl基因家族蛋白表达之间无统计学相关性,其他凋亡抑制因子可能参与原发性中枢神经系统淋巴瘤的发病机制。