Jiang Kun, Tan Elaine, Sayegh Zena, Centeno Barbara, Malafa Mokenge, Coppola Domenico
*Department of Anatomic Pathology †Tissue Core ‡Gastrointestinal Surgical Oncology Program §Tumor Biology and Chemical Biology & Molecular Medicine Programs, Moffitt Cancer Center and Research Institute, Tampa, FL.
Appl Immunohistochem Mol Morphol. 2017 Oct;25(9):620-623. doi: 10.1097/PAI.0000000000000368.
Pancreatic ductal adenocarcinoma (PDAC) is an aggressive carcinoma, with most patients diagnosed at an advanced stage, with a 5-year survival rate of around 5%. An urgent need exists for identifying better diagnostic, prognostic, and therapeutic markers for this lethal disease. Recently, CA125 has been identified in PDAC, and the aim of this research is to study the changes in CA125 expression during the progression of benign pancreatic tissue (BPT) to PDAC and to assess its value as a biomarker of tumor growth. To address these questions, the cellular levels of CA125 in BPT and PDAC were measured using immunohistochemistry and compared on the basis of tumor staging, and the tissue microarray technology were constructed using resected pancreatic tissues. The staining reactions for each case were evaluated semiquantitatively using the histologic score system. Our investigation demonstrates a consistent and significant upregulation of CA125 during the transition from BPT to PDAC. We also found a direct correlation between CA125 immunohistochemistry score and tumor stage (P=0.02). In conclusion, our data indicate that CA125 plays a direct role in pancreatic carcinogenesis and suggests that it may eventually be used as a diagnostic and/or prognostic biomarker of pancreatic cancer. Prospective studies are recommended to evaluate further the diagnostic and prognostic capabilities of CA125 in PDAC, and further studies are warranted to assess the use of CA125 as a therapeutic marker.
胰腺导管腺癌(PDAC)是一种侵袭性癌症,大多数患者在晚期被诊断出来,5年生存率约为5%。迫切需要为这种致命疾病确定更好的诊断、预后和治疗标志物。最近,在PDAC中发现了CA125,本研究的目的是研究从良性胰腺组织(BPT)进展为PDAC过程中CA125表达的变化,并评估其作为肿瘤生长生物标志物的价值。为了解决这些问题,使用免疫组织化学方法测量了BPT和PDAC中CA125的细胞水平,并根据肿瘤分期进行了比较,同时利用切除的胰腺组织构建了组织微阵列技术。使用组织学评分系统对每个病例的染色反应进行半定量评估。我们的研究表明,从BPT转变为PDAC的过程中,CA125持续且显著上调。我们还发现CA125免疫组织化学评分与肿瘤分期之间存在直接相关性(P = 0.02)。总之,我们的数据表明CA125在胰腺癌发生过程中起直接作用,并表明它最终可能用作胰腺癌的诊断和/或预后生物标志物。建议进行前瞻性研究,以进一步评估CA125在PDAC中的诊断和预后能力,并且有必要进行进一步研究,以评估CA125作为治疗标志物的用途。