Department of Anatomic Pathology, Kyushu University, Fukuoka, Japan.
Pathobiology. 2017;84(4):192-201. doi: 10.1159/000455194. Epub 2017 Mar 15.
We reported that pancreatic ductal adenocarcinomas (PDACs) without high-grade pancreatic intraepithelial neoplasia (PanIN) in the vicinity had worse prognoses than PDACs with high-grade PanIN. However, the molecular characteristics of PDACs with and without high-grade PanIN have not been compared. The aim of this study is to clarify the molecular characteristics of PDACs with and without high-grade PanIN.
We reviewed all of a consecutive series of 100 patients with PDACs and divided them into 2 groups: the PDACs with PanIN-2 or PanIN-3 in the background (the PanIN-high group, n = 60) and the PDACs without PanIN-2 or PanIN-3 in the background (the PanIN-low group, n = 40). We evaluated the p53, p16, and SMAD4 expressions in the invasive ductal carcinoma (IDC) components by immunohistochemical staining. KRAS mutation was also analyzed in 80 tumors. The PanIN-low group showed significantly more frequent "high p53 expression" and "loss of SMAD4 expression" than the PanIN-high group (p = 0.048 and p = 0.019, respectively). Loss of p16 expression was not significantly different between the groups. The rate of KRAS wild type was significantly higher in the PanIN-low group than the PanIN-high group (p = 0.024).
Our results demonstrated that the molecular characteristics in the PDACs with high-grade PanIN were different from those in the PDACs without high-grade PanIN. PDACs without high-grade PanIN may develop via a pathway other than the PanIN-carcinoma sequence.
我们曾报道过,附近没有高级别胰腺上皮内瘤变(PanIN)的胰腺导管腺癌(PDAC)比伴有高级别 PanIN 的 PDAC 预后更差。然而,目前尚未对伴有和不伴有高级别 PanIN 的 PDAC 的分子特征进行比较。本研究旨在阐明伴有和不伴有高级别 PanIN 的 PDAC 的分子特征。
我们回顾了连续的 100 例 PDAC 患者的所有病例,并将其分为两组:伴有 PanIN-2 或 PanIN-3 的 PDAC(PanIN-高组,n = 60)和不伴有 PanIN-2 或 PanIN-3 的 PDAC(PanIN-低组,n = 40)。我们通过免疫组织化学染色评估了浸润性导管癌(IDC)成分中 p53、p16 和 SMAD4 的表达。还分析了 80 例肿瘤的 KRAS 突变。PanIN-低组中“高 p53 表达”和“SMAD4 表达缺失”的比例显著高于 PanIN-高组(p = 0.048 和 p = 0.019)。两组之间 p16 表达缺失无显著差异。PanIN-低组 KRAS 野生型的比例显著高于 PanIN-高组(p = 0.024)。
我们的结果表明,伴有高级别 PanIN 的 PDAC 的分子特征与不伴有高级别 PanIN 的 PDAC 不同。不伴有高级别 PanIN 的 PDAC 可能通过 PanIN-癌序列以外的途径发展。