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二肽基肽酶IV活性与结直肠癌预后相关。

Dipeptidyl-peptidase IV activity is correlated with colorectal cancer prognosis.

作者信息

Larrinaga Gorka, Perez Itxaro, Sanz Begoña, Beitia Maider, Errarte Peio, Fernández Ainhoa, Blanco Lorena, Etxezarraga María C, Gil Javier, López José I

机构信息

Department of Nursing I, School of Nursing, University of the Basque Country (UPV/EHU), Leioa, Bizkaia, Spain; Department of Physiology, Faculty of Medicine and Dentistry,University of the Basque Country (UPV/EHU), Leioa, Bizkaia, Spain; BioCruces Health Research Institute, Barakaldo, Bizkaia, Spain.

Department of Physiology, Faculty of Medicine and Dentistry,University of the Basque Country (UPV/EHU), Leioa, Bizkaia, Spain; BioCruces Health Research Institute, Barakaldo, Bizkaia, Spain.

出版信息

PLoS One. 2015 Mar 19;10(3):e0119436. doi: 10.1371/journal.pone.0119436. eCollection 2015.

DOI:10.1371/journal.pone.0119436
PMID:25790122
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4366149/
Abstract

BACKGROUND

Dipeptidyl-peptidase IV (EC 3.4.14.5) (DPPIV) is a serine peptidase involved in cell differentiation, adhesion, immune modulation and apoptosis, functions that control neoplastic transformation. Previous studies have demonstrated altered expression and activity of tissue and circulating DPPIV in several cancers and proposed its potential usefulness for early diagnosis in colorectal cancer (CRC).

METHODS AND PRINCIPAL FINDINGS

The activity and mRNA and protein expression of DPPIV was prospectively analyzed in adenocarcinomas, adenomas, uninvolved colorectal mucosa and plasma from 116 CRC patients by fluorimetric, quantitative RT-PCR and immunohistochemical methods. Results were correlated with the most important classic pathological data related to aggressiveness and with 5-year survival rates. Results showed that: 1) mRNA levels and activity of DPPIV increased in colorectal neoplasms (Kruskal-Wallis test, p<0.01); 2) Both adenomas and CRCs displayed positive cytoplasmic immunostaining with luminal membrane reinforcement; 3) Plasmatic DPPIV activity was lower in CRC patients than in healthy subjects (Mann-U test, p<0.01); 4) Plasmatic DPPIV activity was associated with worse overall and disease-free survivals (log-rank p<0.01, Cox analysis p<0.01).

CONCLUSION/SIGNIFICANCE: 1) Up-regulation of DPPIV in colorectal tumors suggests a role for this enzyme in the neoplastic transformation of colorectal tissues. This finding opens the possibility for new therapeutic targets in these patients. 2) Plasmatic DPPIV is an independent prognostic factor in survival of CRC patients. The determination of DPPIV activity levels in the plasma may be a safe, minimally invasive and inexpensive way to define the aggressiveness of CRC in daily practice.

摘要

背景

二肽基肽酶IV(EC 3.4.14.5)(DPPIV)是一种丝氨酸肽酶,参与细胞分化、黏附、免疫调节和细胞凋亡,这些功能控制着肿瘤转化。先前的研究已经证明,在几种癌症中,组织和循环中的DPPIV表达和活性发生了改变,并提出其在结直肠癌(CRC)早期诊断中的潜在用途。

方法和主要发现

通过荧光法、定量逆转录聚合酶链反应和免疫组织化学方法,对116例CRC患者的腺癌、腺瘤、未受累的结直肠黏膜和血浆中的DPPIV活性、mRNA和蛋白质表达进行了前瞻性分析。结果与与侵袭性相关的最重要的经典病理数据以及5年生存率相关。结果显示:1)结直肠肿瘤中DPPIV的mRNA水平和活性增加(Kruskal-Wallis检验,p<0.01);2)腺瘤和CRC均显示细胞质免疫染色阳性,伴有腔膜增强;3)CRC患者的血浆DPPIV活性低于健康受试者(Mann-U检验,p<0.01);4)血浆DPPIV活性与较差的总生存率和无病生存率相关(对数秩检验p<0.01,Cox分析p<0.01)。

结论/意义:1)结直肠肿瘤中DPPIV的上调表明该酶在结直肠组织的肿瘤转化中起作用。这一发现为这些患者的新治疗靶点开辟了可能性。2)血浆DPPIV是CRC患者生存的独立预后因素。测定血浆中DPPIV活性水平可能是在日常实践中确定CRC侵袭性的一种安全、微创且廉价的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5570/4366149/fca0633a3123/pone.0119436.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5570/4366149/2d05f1d7d092/pone.0119436.g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5570/4366149/107f7a33b179/pone.0119436.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5570/4366149/b22b68f36f41/pone.0119436.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5570/4366149/462000b8d8d8/pone.0119436.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5570/4366149/00fcda3007ef/pone.0119436.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5570/4366149/fca0633a3123/pone.0119436.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5570/4366149/2d05f1d7d092/pone.0119436.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5570/4366149/ed6eb34856a8/pone.0119436.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5570/4366149/107f7a33b179/pone.0119436.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5570/4366149/b22b68f36f41/pone.0119436.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5570/4366149/462000b8d8d8/pone.0119436.g005.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5570/4366149/fca0633a3123/pone.0119436.g007.jpg

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