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凋亡相关基因bax和bcl-2在卵巢癌中的差异表达。

Differential expression of apoptosis associated genes bax and bcl-2 in ovarian cancer.

作者信息

Marx D, Binder C, Meden H, Lenthe T, Ziemek T, Hiddemann T, Kuhn W, Schauer A

机构信息

Department of Pathology, University of Göttingen, Germany.

出版信息

Anticancer Res. 1997 May-Jun;17(3C):2233-40.

PMID:9216694
Abstract

The prognostic value of various molecular markers, which adequately account for the tumor biology and disease behaviour of ovarian cancer, is still unclear. Recent studies have focused on the role of genes regulating the balance between proliferation and cellular suicide, apoptosis. In the present study, tumor tissue from 215 patients with ovarian cancer was immunohistochemically analysed for Bax- and Bcl-2-expression. There was an association between Bcl-2-expression (30%) and factors of favourable prognosis. In contrast, Bax-expression (47%) was related to bad clinical outcome, especially in cases without concomitant Bcl-2-expression. In patients with Bcl-2-positive/Bax-negative tumors, overall survival was significantly longer (p = 0.0379) than in patients with Bcl-2- and Bax-negative tumors. Respectively, expression of Bax without Bcl-2-expression was correlated with bad clinical outcome (p = 0.033). The difference in overall survival was most striking (p = 0.0007) between patients with Bax-positive/Bcl-2-negative and Bcl-2-positive/Bax-negative tumors. This could also be demonstrated for the various subgroups of different tumor grade and stage. It may be speculated, that alteration of the Bax/Bcl-2-balance may influence the clinical course by deregulation of programmed cell death and altered sensitivity to chemotherapy.

摘要

各种分子标志物对卵巢癌肿瘤生物学和疾病行为的充分评估的预后价值仍不清楚。最近的研究集中在调节细胞增殖与细胞自杀(即凋亡)之间平衡的基因的作用上。在本研究中,对215例卵巢癌患者的肿瘤组织进行了Bax和Bcl-2表达的免疫组化分析。Bcl-2表达(30%)与预后良好的因素之间存在关联。相比之下,Bax表达(47%)与不良临床结局相关,尤其是在没有伴随Bcl-2表达的情况下。在Bcl-2阳性/Bax阴性肿瘤患者中,总生存期显著长于(p = 0.0379)Bcl-2和Bax均阴性的患者。分别地,无Bcl-2表达的Bax表达与不良临床结局相关(p = 0.033)。Bax阳性/Bcl-2阴性和Bcl-2阳性/Bax阴性肿瘤患者之间的总生存期差异最为显著(p = 0.0007)。这在不同肿瘤分级和分期的各个亚组中也得到了证实。可以推测,Bax/Bcl-2平衡的改变可能通过程序性细胞死亡的失调和化疗敏感性的改变来影响临床病程。

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