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下调 Bax 相互作用因子 1 在人胰腺导管腺癌中的表达。

Down-regulation of Bax-interacting factor 1 in human pancreatic ductal adenocarcinoma.

机构信息

Department of Anatomic Pathology, University of South Florida, Tampa, FL, USA.

出版信息

Pancreas. 2011 Apr;40(3):433-7. doi: 10.1097/MPA.0b013e318205eb03.

Abstract

OBJECTIVE

Bax-interacting factor 1 (Bif-1) protein plays a critical role in apoptosis, mitochondrial morphogenesis, and autophagy, and its loss promotes tumorigenesis. The role of Bif-1 in pancreatic cancer has not been studied.

METHODS

We determined Bif-1 expression in 82 human pancreatic ductal adenocarcinomas (PDCs) and in 82 nonmalignant pancreatic specimens (NMPs), using immunohistochemistry and tissue microarray. Bif-1 immunostain was semiquantitatively scored on a scale of 0 to 9.

RESULTS

Bif-1 scores in NMP were either 6 or 9, with lower scores in only 19 (23.2%) of 82 NMPs. Low Bif-1 expression (score <6) was found in 37 (45.1%) of 82 PDCs, a proportion significantly greater than that found in NMP (P = 0.005). The expression of Bif-1 was twice as likely to be low in PDC as in NMP (relative risk = 1.95, 95% confidence interval, 1.23-3.09). Kaplan-Meier survival estimates showed no difference in survival between patients with low and high Bif-1 expression (P = 0.21, log-rank test).

CONCLUSIONS

The expression of Bif-1 is downregulated in a subset of PDC. This novel finding is in agreement with the tumor suppressor function of Bif-1. The lack of association between Bif-1 expression and patient survival may be best explained by the complexity of carcinogenesis.

摘要

目的

Bax 相互作用因子 1(Bif-1)蛋白在细胞凋亡、线粒体形态发生和自噬中发挥关键作用,其缺失可促进肿瘤发生。Bif-1 在胰腺癌中的作用尚未被研究过。

方法

我们通过免疫组织化学和组织微阵列检测了 82 例人胰腺导管腺癌(PDC)和 82 例非恶性胰腺标本(NMP)中的 Bif-1 表达。Bif-1 免疫染色评分范围为 0 至 9。

结果

NMP 的 Bif-1 评分要么为 6,要么为 9,只有 19 例(23.2%)NMP 的评分较低。在 82 例 PDC 中,有 37 例(45.1%)存在低 Bif-1 表达(评分<6),这一比例明显高于 NMP(P=0.005)。Bif-1 在 PDC 中的表达比在 NMP 中低两倍的可能性(相对风险=1.95,95%置信区间,1.23-3.09)。Kaplan-Meier 生存估计显示,低和高 Bif-1 表达患者的生存无差异(P=0.21,对数秩检验)。

结论

Bif-1 的表达在部分 PDC 中下调。这一新发现与 Bif-1 的肿瘤抑制功能一致。Bif-1 表达与患者生存之间缺乏关联,这可能最好用致癌作用的复杂性来解释。

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