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磷脂酰乙醇胺结合蛋白 1 下调与胆囊癌临床意义的相关性研究。

Clinical Significance of Frequently Down-Regulated Phosphatidylethanolamine-Binding Protein-1 in Gallbladder Cancer.

机构信息

Department of Zoology, Mahila Mahavidyalaya, Banaras Hindu University, Varanasi, 221005, India.

Department of General Surgery, Institute of Medical Sciences, Banaras Hindu University, Varanasi, 221005, India.

出版信息

Dig Dis Sci. 2024 Feb;69(2):502-509. doi: 10.1007/s10620-023-08216-5. Epub 2023 Dec 22.

Abstract

BACKGROUND

Promoter hypermethylation of tumor suppressor genes has been demonstrated to be one of the major mechanisms of their epigenetic regulation in various reports. We have studied the promoter methylation status of PEBP1 and evaluated its correlation with gallbladder carcinogenesis.

AIMS

PEBP1, an endogenous inhibitor of Raf/MEK/ERK signaling pathway, is a tumor suppressor gene. We aimed to study the expression profile of PEBP1 and understand the mechanism and significance of its deregulation in gallbladder cancer.

METHODS

PEBP1 expression analysis and its promoter methylation status were investigated in 77 gallbladder carcinoma (GBC) and tissue biopsies from 28 patients of gallstone disease by RT-PCR and MS-PCR, respectively.

RESULTS

Our results of the mRNA expression profiling demonstrate that PEBP1 is down-regulated in 62.3% (48/77), while 31.2% (24/77) of the gallbladder cancer biopsies show no significant change and 6.5% (5/77) show up-regulated expression compared to tissue samples of gallstone diseases. In GBC, 48.1% (N = 37) GBC biopsy samples exhibited significantly heterozygous promoter hypermethylation compared to tissue samples from gallstone diseases which show promoter hypermethylation in 3 (10.7%) samples only. In gallbladder cancer, the PEBP1 methylation is significantly associated with lymph node metastasis and shorter period of survival.

CONCLUSION

PEBP1 is frequently down-regulated and hypermethylated in gallbladder cancer and its promoter hypermethylation is a frequent and early inactivating mechanism in GBC.

摘要

背景

在各种报道中,肿瘤抑制基因的启动子超甲基化已被证明是其表观遗传调控的主要机制之一。我们研究了 PEBP1 的启动子甲基化状态,并评估了其与胆囊癌发生的相关性。

目的

PEBP1 是 Raf/MEK/ERK 信号通路的内源性抑制剂,是一种肿瘤抑制基因。我们旨在研究 PEBP1 的表达谱,了解其在胆囊癌中失调的机制和意义。

方法

通过 RT-PCR 和 MS-PCR 分别检测 77 例胆囊癌(GBC)和 28 例胆囊疾病患者组织活检中 PEBP1 的表达分析及其启动子甲基化状态。

结果

我们的 mRNA 表达谱结果表明,PEBP1 在 62.3%(48/77)的病例中下调,而 31.2%(24/77)的病例无明显变化,6.5%(5/77)的病例上调。在 GBC 中,48.1%(N=37)的 GBC 活检样本与胆囊疾病组织样本相比表现出显著的杂合启动子超甲基化,而胆囊疾病组织样本中只有 3 个样本(10.7%)表现出启动子超甲基化。在胆囊癌中,PEBP1 甲基化与淋巴结转移和生存时间较短显著相关。

结论

PEBP1 在胆囊癌中经常下调和超甲基化,其启动子超甲基化是 GBC 中一种常见且早期的失活机制。

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