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Expression of Beclin 1 and Bcl-2 in pancreatic neoplasms and its effect on pancreatic ductal adenocarcinoma prognosis

机译:Beclin 1和Bcl-2在胰腺肿瘤中的表达及其对胰腺导管腺癌预后的影响

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摘要

Aberrant expression of Beclin 1 and B-cell lymphoma-2 (Bcl-2) has been identified in a variety of human tumors; however, little information is available for pancreatic neoplasms. The present study analyzed the expression of Beclin 1 and Bcl-2 in pancreatic ductal adenocarcinoma (PDAC) and solid pseudopapillary neoplasm (SPN) of the pancreas, and evaluated their prognostic significance for PDAC. The present study included 117 PDAC, 43 SPN and 32 chronic pancreatitis (CP) cases. Levels of Beclin 1 and Bcl-2 expression were evaluated semiquantitatively by immunohistochemistry, and their correlation with the survival of patients with PDAC was determined. Beclin 1 was upregulated in 74 (63.2%) PDAC, 26 (60.5%) SPN, and 14 (43.8%) CP cases. Bcl-2 was upregulated in 38 (32.5%) PDAC, 11 (25.6%) SPN and 24 (75.0%) CP cases. High Beclin 1 and low Bcl-2 expression was significantly correlated with poor differentiation and distant metastasis in PDAC, and associated with the presence of nuclear pleomorphism in SPN and with advanced Tumor-Node-Metastasis stage in PDAC. Beclin 1 and Bcl-2 levels were inversely correlated in PDAC, whereas they were positively correlated in SPN. Low Beclin 1 and high Bcl-2 expression was associated with improved disease-free survival and overall survival (OS). However, the association of Beclin 1 with survival was not significant in the Cox analysis, whereas Bcl-2 expression was significantly correlated with OS in the multivariate analysis. In conclusion, Beclin 1 upregulation exacerbated the progression and aggressiveness of pancreatic neoplasms, and Bcl-2 downregulated expression was an independently poor prognostic factor for PDAC.
机译:已经在多种人类肿瘤中发现了Beclin 1和B细胞淋巴瘤2(Bcl-2)的异常表达。但是,有关胰腺肿瘤的信息很少。本研究分析了Beclin 1和Bcl-2在胰腺胰管腺癌(PDAC)和胰腺实体假乳头状瘤(SPN)中的表达,并评估了其对PDAC的预后意义。本研究包括117例PDAC,43例SPN和32例慢性胰腺炎(CP)病例。通过免疫组织化学方法半定量评估Beclin 1和Bcl-2表达水平,并确定它们与PDAC患者生存率的相关性。 Beclin 1在74例(63.2%)PDAC,26例(60.5%)SPN和14例(43.8%)CP病例中上调。 Bcl-2在38例(32.5%)PDAC,11例(25.6%)SPN和24例(75.0%)CP病例中上调。高Beclin 1和低Bcl-2表达与PDAC中差的分化和远处转移显着相关,并与SPN中核多态性的存在和PDAC中晚期肿瘤-结节转移阶段有关。 Beclin 1和Bcl-2水平在PDAC中呈负相关,而在SPN中则呈正相关。 Beclin 1的低表达和Bcl-2的高表达与无病生存期和总生存期(OS)改善有关。但是,在Cox分析中,Beclin 1与生存的相关性不显着,而在多变量分析中,Bcl-2表达与OS显着相关。总之,Beclin 1的上调加剧了胰腺肿瘤的进展和侵袭性,而Bcl-2的下调是PDAC的独立不良预后因素。

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