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首页> 外文期刊>Human Pathology >CRABP-II is a highly sensitive and specific diagnostic molecular marker for pancreatic ductal adenocarcinoma in distinguishing from benign pancreatic conditions
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CRABP-II is a highly sensitive and specific diagnostic molecular marker for pancreatic ductal adenocarcinoma in distinguishing from benign pancreatic conditions

机译:CRABP-II是胰腺管腺癌与良性胰腺疾病相区分的高度灵敏和特异性的诊断分子标记

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摘要

CRABP-II, a retinoic acid binding protein, shuffles retinoic acid from cytoplasm into nucleus and forms a complex with nuclear retinoic acid receptor to facilitate transcriptional activities of retinoic acid. In this study, we studied the expression patterns of CRABP-II in pancreatic ductal adenocarcinoma (PDAC) compared with those in normal pancreas, chronic pancreatitis, and precancerous lesions. We showed no detectable expressions of CRABP-II in normal pancreatic parenchyma, normal ductal epithelium, and chronic pancreatitis. In contrast, the expression of CRABP-II was readily detected in all PDACs including metastatic PDACs. CRABP-II staining was also observed and progressively increased from pancreatic intraepithelial neoplasia 1 to 3. In addition, when fine needle aspiration specimens were evaluated from patients with PDAC, CRABP-II was positive in 55.6% cases if cytology diagnosis was "atypia," and in 87.5% cases, if "malignancy." Our study suggests that CRABP-II is highly and specifically expressed in PDAC and is more commonly expressed in high-grade precursor cancerous lesions than in low-grade lesions. Therefore, overexpression of CRABP-II is a late event of pancreatic carcinogenesis, and it could be used as a diagnostic marker to distinguish PDAC from other benign pancreatic conditions in both resection and cytology specimens.
机译:CRABP-II是一种视黄酸结合蛋白,可将视黄酸从细胞质改组为核,并与视黄酸核受体形成复合物,从而促进视黄酸的转录活性。在这项研究中,我们研究了CRABP-II在胰腺导管腺癌(PDAC)与正常胰腺,慢性胰腺炎和癌前病变中的表达模式。我们显示正常胰腺实质,正常导管上皮和慢性胰腺炎中均未检测到CRABP-II的表达。相反,在包括转移性PDAC在内的所有PDAC中都容易检测到CRABP-II的表达。还观察到CRABP-II染色,并从胰腺上皮内瘤变1​​到3逐渐增加。另外,当从PDAC患者中评估细针穿刺标本时,如果细胞学诊断为“非典型”,则CRABP-II阳性的占55.6%。在87.5%的情况下为“恶性”。我们的研究表明,CRABP-II在PDAC中高度特异性地表达,在高级别的前体癌性病变中比在低级别的病变中更常见。因此,CRABP-II的过表达是胰腺癌发生的晚期事件,在切除和细胞学标本中,CRABP-II可用作诊断标志物,以区分PDAC与其他良性胰腺疾病。

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