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Pathogenesis of multiple pancreatic cancers involves multicentric carcinogenesis and intrapancreatic metastasis

机译:多种胰腺癌的发病机制涉及多中心癌变和胰腺内转移

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摘要

There are increased opportunities in oncology clinics to identify multiple pancreatic ductal adenocarcinomas (PDAC) that co‐occur simultaneously or arise metachronously in the pancreatic parenchyma, yet their pathogenesis remains elusive. We hypothesized that two potential pathways, multicentric carcinogenesis and intrapancreatic metastasis, might contribute to forming multiple PDAC. Among 241 resected cases, we identified 20 cancer nodules from nine patients with multiple PDAC (six with synchronous PDAC, one with metachronous PDAC, and two with both synchronous and metachronous PDAC). Integrated clinical, pathological, and mutational analyses, using TP53 and SMAD4 immunostaining and targeted next‐generation sequencing of 50 cancer‐related genes, were conducted to examine the intertumor relationships. Four of the nine patients were assessed as having undergone multicentric carcinogenesis because of heterogeneity of immunohistochemical and/or mutation characteristics. In contrast, tumors in the other five patients showed intertumor molecular relatedness. Two of these five patients, available for matched sequencing data, showed two or more shared mutations. Moreover, all the smaller nodules in these five patients showed identical TP53 and SMAD4 expression patterns to the corresponding main tumors. Consequently, these five patients were considered to have undergone intrapancreatic metastasis. None of the five smaller nodules arising from intrapancreatic metastasis was accompanied by pancreatic intraepithelial neoplasia, and three of them were tiny (≤1mm). Patients whose tumors resulted from intrapancreatic metastasis appeared to have higher disease stages and worse outcome than those with tumors from multicentric carcinogenesis. Our results provide insight into pancreatic carcinogenesis, showing that the development of multiple PDAC involves distinct evolutionary paths that potentially affect patient prognosis.
机译:肿瘤诊所中鉴定出同时发生于胰腺实质或同时发生于胰腺实质中的多个胰腺导管腺癌(PDAC)的机会越来越多,但其发病机理仍然难以捉摸。我们假设两个潜在的途径,多中心癌变和胰腺内转移,可能有助于形成多个PDAC。在241例切除的病例中,我们从9例多发PDAC患者中识别出20个癌结节(6例为同步PDAC,1例为同步PDAC,2例为同步和同步PDAC)。使用TP53和SMAD4免疫染色以及针对50个与癌症相关的基因的下一代测序进行了综合的临床,病理和突变分析,以检查肿瘤之间的关系。由于免疫组化和/或突变特征的异质性,将九名患者中的四名评估为经历了多中心癌变。相反,其他五名患者的肿瘤表现出肿瘤间分子相关性。这五名患者中有两名可用于匹配的测序数据,显示出两个或多个共享突变。此外,这五名患者中所有较小的结节均显示与相应的主要肿瘤相同的TP53和SMAD4表达模式。因此,这五名患者被认为已发生胰腺内转移。胰腺内转移引起的五个较小结节中没有一个伴有胰腺上皮内瘤变,其中三个很小(≤1mm)。与多中心致癌肿瘤相比,胰腺内转移引起的肿瘤患者的疾病分期更高,预后更差。我们的结果提供了对胰腺癌发生的认识,表明多种PDAC的发展涉及可能影响患者预后的独特进化途径。

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