Home HOME General Physiology and Biophysics 2022 General Physiology and Biophysics Vol.41, No.1, p. 15–30, 2022

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Founded: 1982
ISSN 1338-4325 (online)
ISSN 0231-5882 (print)
Published in English,
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General Physiology and Biophysics Vol.41, No.1, p. 15–30, 2022

Title: Identification of hub genes in chronic pancreatitis and analysis of association with pancreatic cancer via bioinformatic analysis
Author: Hongxuan Li, Chenjun Hao, Qiu Yang, Wenqi Gao, Biao Ma, Dongbo Xue

Abstract: hronic pancreatitis (CP), a fibroinflammatory disease, is a potential risk factor for pancreatic cancer. This study attempted to identify and analyze the key genes involved in CP development and their association with pancreatic cancer. The GSE41418 dataset was obtained from the Gene Expression Omnibus database. Gene ontology and Kyoto Encyclopedia of Genes and Genomes pathway analyses were performed on common differentially expressed genes. A protein-protein interaction network was constructed by using the STRING database. The expression and prognostic value of hub genes in pancreatic cancer were analyzed by Gene Expression Profiling Interactive Analysis (GEPIA) and UALCAN databases. The results showed that the upregulated genes primarily focused on the cell cycle, DNA replication, and phagosome activity. The PPI network was composed of 184 nodes and 925 edges. The 10 hub genes were screened by CytoHubba, of which CCNB2, CDC6, CDK1 and CKS2 were observed to be differentially expressed in pancreatic cancer with CP, and all of them were detrimental to overall survival and recurrence-free survival of pancreatic cancer. In this study, we employed bioinformatic analysis to determine that CCNB2, CDC6, CDK1 and CKS2 may be key genes in the development of CP and pancreatic cancer.

Keywords: Chronic pancreatitis — Pancreatic cancer — GEPIA — UALCAN — Prognostic value
Published online: 14-Feb-2022
Year: 2022, Volume: 41, Issue: 1 Page From: 15, Page To: 30
doi:10.4149/gpb_2021033


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