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垂体腺苷酸环化酶激活肽及PAC1受体在胰腺导管癌中的表达

PACAP and PAC1 receptor expression in pancreatic ductal carcinoma.

作者信息

Ferencz Sandor, Reglodi Dora, Kaszas Balint, Bardosi Attila, Toth Denes, Vekony Zsofia, Vicena Viktoria, Karadi Oszkar, Kelemen Dezso

机构信息

Department of Surgery, University of Pécs, Medical School, Pécs 7622, Hungary.

Department of Anatomy, MTA-PTE PACAP Research Group, University of Pécs, Medical School, Pécs 7622, Hungary.

出版信息

Oncol Lett. 2019 Dec;18(6):5725-5730. doi: 10.3892/ol.2019.10971. Epub 2019 Oct 8.

DOI:10.3892/ol.2019.10971
PMID:31788045
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6865831/
Abstract

Pancreatic carcinoma is one of the most malignant diseases and is associated with a poor survival rate. Pituitary adenylate cyclase activating polypeptide (PACAP) is a neuropeptide that acts on three different G protein-coupled receptors: the specific PAC1 and the VPAC1/2 that also bind vasoactive intestinal peptide. PACAP is widely distributed in the body and has diverse physiological effects. Among other things, it acts as a trophic factor and influences proliferation and differentiation of several different cells both under normal circumstances and tumourous transformation. Changes of PACAP and its receptors have been shown in various tumour types. However, it is not known whether PACAP and its specific receptor are altered in pancreatic cancer. Perioperative data of patients with pancreas carcinoma was investigated over a five-year period. Histological results showed Grade 2 or Grade 3 adenocarcinoma in most cases. PACAP and PAC1 receptor expression were investigated by immunohistochemistry. Staining intensity of PAC1 receptor was strong in normal tissues both in the exocrine and endocrine parts of the pancreas, the receptor staining was markedly weaker in the adenocarcinoma. PACAP immunostaining was weak in the exocrine part and very strong in the islets and nerve elements in non-tumourous tissues. The PACAP immunostaining almost disappeared in the adenocarcinoma samples. Based on these findings a decrease or lack of the PAC1 receptor/PACAP signalling might have an influence on tumour growth and/or differentiation.

摘要

胰腺癌是最具恶性的疾病之一,生存率很低。垂体腺苷酸环化酶激活多肽(PACAP)是一种神经肽,作用于三种不同的G蛋白偶联受体:特异性PAC1以及也结合血管活性肠肽的VPAC1/2。PACAP广泛分布于体内,具有多种生理作用。其中,它作为一种营养因子,在正常情况下以及肿瘤转化过程中影响几种不同细胞的增殖和分化。PACAP及其受体的变化已在多种肿瘤类型中得到证实。然而,尚不清楚PACAP及其特异性受体在胰腺癌中是否发生改变。对胰腺癌患者的围手术期数据进行了为期五年的调查。组织学结果显示,大多数病例为2级或3级腺癌。通过免疫组织化学研究PACAP和PAC1受体的表达。PAC1受体在胰腺外分泌和内分泌部分的正常组织中染色强度较强,在腺癌中受体染色明显较弱。PACAP免疫染色在非肿瘤组织的外分泌部分较弱,在胰岛和神经成分中非常强。在腺癌样本中,PACAP免疫染色几乎消失。基于这些发现,PAC1受体/PACAP信号的减少或缺失可能会影响肿瘤的生长和/或分化。

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The Neuroprotective and Biomarker Potential of PACAP in Human Traumatic Brain Injury.PACAP 在人类创伤性脑损伤中的神经保护和生物标志物潜力。
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