Tadic Mario, Stoos-Veic Tajana, Kujundzic Milan, Turcic Petra, Aralica Gorana, Boskoski Ivo
Department of Gastroenterology, Dubrava University Hospital.
University of Zagreb Faculty of Pharmacy and Biochemistry.
Eur J Gastroenterol Hepatol. 2020 Apr;32(4):496-500. doi: 10.1097/MEG.0000000000001696.
Despite numerous investigations, we still do not have a specific marker for pancreatic ductal adenocarcinoma. Only guideline-recommended biomarker for pancreatic ductal adenocarcinoma is the CA19-9, but it is also present in other gastrointestinal diseases. IMP3 is a new potential biomarker that is over-expressed in some cancers. The aims of our study were (1) to assess IMP3 in benign pancreatic lesions and pancreatic cancer, and (2) to estimate its concentrations in localized and advanced pancreatic cancer.
Seventy-five patients with solid pancreatic lesions who underwent EUS-FNA were included. Patients were divided into three groups: benign lesions, cancer localized only on the pancreas, and patients with advanced pancreatic cancer (locally advanced or with distal metastases). Immunoreactivity of IMP3 was assessed on cytological smears sampled by endoscopic ultrasound.
IMP3 was expressed in 89% of the patients with pancreatic cancer and not in benign lesions. Stronger expression of IMP3 protein and stage of the pancreatic cancer was statistically significant. IMP3 was expressed in all localized cancers and in 85% of patients with advanced pancreatic cancer. In the subgroup with locally advanced cancer, IMP3 was expressed in 88%, and in 83% of patients in the subgroup with distal metastasis (P = 0.007). In the present study, sensitivity was 89%, specificity 100%, with positive predictive value of 100% and negative predictive value of 63%.
There is a positive correlation between IMP3 expression and TNM stages of the pancreatic cancer. Higher expression of IMP3 on EUS-FNA specimens can suggest poorer prognosis.
尽管进行了大量研究,但我们仍未找到胰腺导管腺癌的特异性标志物。胰腺导管腺癌唯一被指南推荐的生物标志物是CA19-9,但它也存在于其他胃肠道疾病中。IMP3是一种新的潜在生物标志物,在某些癌症中过度表达。我们研究的目的是:(1)评估IMP3在胰腺良性病变和胰腺癌中的情况;(2)估计其在局限性和晚期胰腺癌中的浓度。
纳入75例接受超声内镜引导下细针穿刺(EUS-FNA)的胰腺实性病变患者。患者分为三组:良性病变组、仅胰腺局部癌变组和晚期胰腺癌患者组(局部进展期或有远处转移)。通过内镜超声采集的细胞学涂片评估IMP3的免疫反应性。
IMP3在89%的胰腺癌患者中表达,在良性病变中不表达。IMP3蛋白的更强表达与胰腺癌分期在统计学上具有显著相关性。IMP3在所有局限性癌症以及85%的晚期胰腺癌患者中表达。在局部进展期癌症亚组中,88%的患者表达IMP3,在远处转移亚组中83%的患者表达IMP3(P = 0.007)。在本研究中,敏感性为89%,特异性为100%,阳性预测值为100%,阴性预测值为63%。
IMP3表达与胰腺癌的TNM分期之间存在正相关。超声内镜引导下细针穿刺标本上IMP3的高表达提示预后较差。