Department of Anatomic Pathology, Graduate School of Medical Sciences, Kyushu University, Fukuoka 812-8582, Japan.
Hum Pathol. 2013 Sep;44(9):1714-21. doi: 10.1016/j.humpath.2012.12.020. Epub 2013 Apr 15.
Recently, various studies have shown that insulin-like growth factor II messenger RNA-binding protein-3 (IMP3) is a useful diagnostic marker for malignant lesions and a prognostic marker for poor survival in several kinds of tumors. However, the value of IMP3 as a diagnostic and prognostic marker in intraductal papillary mucinous neoplasm (IPMN) of pancreas has been unclear until now. In this study, we examined IMP3 immunohistochemical expression in 190 resection samples and 15 biopsy samples of IPMN and analyzed the value of IMP3 as a diagnostic and prognostic marker. IMP3 expression was recognized in 71.8% (28/39) of IPMNs with high-grade dysplasia and in 81.3% (26/32) of IPMNs with an associated invasive carcinoma (IPMN-IC), but it was not found in any IPMNs with low-grade dysplasia or in IPMNs with intermediate dysplasia. IMP3 expression was significantly higher in cancerous lesions (IPMN with high-grade dysplasia and IPMN-IC) than in noncancerous lesions (IPMN with low-grade dysplasia and IPMN with intermediate-grade dysplasia), with a sensitivity of 76.1% and a specificity of 100% (P < .001). We also identified a significant difference in IMP3 expression between cancerous lesions and noncancerous lesions in biopsy specimens (P = .027). In IPMN-IC, disease-specific survival was significantly shorter in the high-expression group (>50% tumor staining) than in the low-expression group (≤50% tumor staining; P = .0069). In conclusion, our findings show that IMP3 is a useful diagnostic marker for distinguishing between noncancerous and cancerous lesions and is a valuable prognostic biomarker in IPMN.
最近,各种研究表明胰岛素样生长因子 II 信使 RNA 结合蛋白 3(IMP3)是多种肿瘤恶性病变的有用诊断标志物和预后不良的标志物。然而,直到现在,IMP3 作为胰腺导管内乳头状黏液性肿瘤(IPMN)的诊断和预后标志物的价值仍不清楚。在这项研究中,我们检测了 190 例手术切除样本和 15 例活检样本中 IMP3 的免疫组化表达,并分析了 IMP3 作为诊断和预后标志物的价值。在高级别异型增生的 IPMN 中,有 71.8%(28/39)的肿瘤表达 IMP3,在伴有浸润性癌的 IPMN 中,有 81.3%(26/32)的肿瘤表达 IMP3,但在低级别异型增生的 IPMN 中或中级异型增生的 IPMN 中均未发现 IMP3 表达。在癌性病变(高级别异型增生的 IPMN 和 IPMN-IC)中,IMP3 的表达明显高于非癌性病变(低级别异型增生的 IPMN 和中级异型增生的 IPMN),其敏感性为 76.1%,特异性为 100%(P<.001)。我们还发现活检标本中癌性病变和非癌性病变之间的 IMP3 表达有显著差异(P=0.027)。在 IPMN-IC 中,高表达组(>50%肿瘤染色)的疾病特异性生存率明显短于低表达组(≤50%肿瘤染色;P=0.0069)。综上所述,我们的研究结果表明,IMP3 是一种鉴别良恶性病变的有用诊断标志物,是 IPMN 有价值的预后生物标志物。