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细胞外基质是胰腺导管腺癌早期的主要靶向环境。

Extracellular matrix is the main targeted environment in early stage of pancreatic ductal adenocarcinoma.

作者信息

Mansouri Vahid, Arjmand Babak, Hamzeloo-Moghadam Maryam, Razzaghi Zahra, Ahmadzadeh Alireza, Ehsani Ardakani Mohammad Javad, Mohamoud Robati Reza

机构信息

Proteomics Research Center, Faculty of Paramedical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Cell Therapy and Regenerative Medicine Research Center, Endocrinology and Metabolism Molecular-Cellular Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Gastroenterol Hepatol Bed Bench. 2023;16(4):401-407. doi: 10.22037/ghfbb.v16i4.2859.

DOI:10.22037/ghfbb.v16i4.2859
PMID:38313356
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10835096/
Abstract

AIM

Due to weak diagnosis and treatment of pancreatic ductal adenocarcinoma (PDAC), detection of PDAC possible biomarkers in early stage is the main aim of this study.

BACKGROUND

PDAC is known as an exocrine cancer with a 5-year overall survival of 11%.

METHODS

Gene expression profiles of early stage of PDAC tissue and normal tissue are downloaded from gene expression omnibus (GEO) and evaluated via GEO2R. The significant differentially expressed genes (DEGs) are investigated via protein-protein interaction (PPI) network analysis and gene ontology.

RESULTS

Among 104 DEGs, ALB, COL1A1, COL1A2, MMP1, POSTN, PLAU, and COL3A1 were pointed out as hub nodes. "Gelatin degradation by MMP1, 2, 3, 7, 8, 9, 12, 13" group of 52 biological terms were identified as the main affected terms.

CONCLUSION

In conclusion, ALB, MMP1, and COL1A1 genes were highlighted as possible biomarkers of early stage of PDAC. Dysfunction of extracellular matrix was identified as a main event in patients.

摘要

目的

由于胰腺导管腺癌(PDAC)的诊断和治疗手段有限,本研究的主要目的是探寻PDAC早期可能的生物标志物。

背景

PDAC是一种外分泌腺癌,其5年总生存率为11%。

方法

从基因表达综合数据库(GEO)下载PDAC组织和正常组织早期的基因表达谱,并通过GEO2R进行评估。通过蛋白质-蛋白质相互作用(PPI)网络分析和基因本体论研究显著差异表达基因(DEG)。

结果

在104个DEG中,白蛋白(ALB)、I型胶原蛋白α1(COL1A1)、I型胶原蛋白α2(COL1A2)、基质金属蛋白酶1(MMP1)、骨膜蛋白(POSTN)、纤溶酶原激活物(PLAU)和III型胶原蛋白α1(COL3A1)被指出是关键节点。52个生物学术语组成的“MMP1、2、3、7、8、9、12、13介导的明胶降解”组被确定为主要受影响的术语。

结论

总之,ALB、MMP1和COL1A1基因被确定为PDAC早期可能的生物标志物。细胞外基质功能障碍被确定为患者的主要病变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2ac/10835096/2168ab9957d5/GHFBB-16-401-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2ac/10835096/a9e680cc998c/GHFBB-16-401-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2ac/10835096/8827f342213a/GHFBB-16-401-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2ac/10835096/765285c86152/GHFBB-16-401-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2ac/10835096/2168ab9957d5/GHFBB-16-401-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2ac/10835096/a9e680cc998c/GHFBB-16-401-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2ac/10835096/8827f342213a/GHFBB-16-401-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2ac/10835096/765285c86152/GHFBB-16-401-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2ac/10835096/2168ab9957d5/GHFBB-16-401-g008.jpg

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Dysregulation of HNF1B/Clusterin axis enhances disease progression in a highly aggressive subset of pancreatic cancer patients.HNF1B/Clusterin 轴的失调增强了高度侵袭性胰腺癌患者亚群的疾病进展。
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COL17A1 facilitates tumor growth and predicts poor prognosis in pancreatic cancer.
Sci Rep. 2025 Apr 11;15(1):12515. doi: 10.1038/s41598-025-97629-5.
COL17A1 促进胰腺癌的生长并预测不良预后。
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COL1A1: A novel oncogenic gene and therapeutic target in malignancies.COL1A1:恶性肿瘤中的一种新的致癌基因和治疗靶点。
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Translational advances in pancreatic ductal adenocarcinoma therapy.胰腺导管腺癌治疗的转化进展。
Nat Cancer. 2022 Mar;3(3):272-286. doi: 10.1038/s43018-022-00349-2. Epub 2022 Mar 29.
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