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Prognostic Relevance of HJURP Expression in Patients with Surgically Resected Colorectal Cancer

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Abstract
HJURP is a key factor for CENP-A deposition and maintenance in centromeres. The role of mis-regulation of histone chaperones in cancer initiation and progression has been studied. However, its role in colorectal cancer is still unclear. In this study, we aimed to evaluate the expression of HJURP in 162 colorectal cancer tissue. To investigate the function of HJURP in the colorectal cancer cell, we suppressed HJURP expression by siRNA and confirmed proliferation, migration, invasion, and anchorage independent of colony forming ability. The association between HJURP expression levels and clinicopathological factors was evaluated in 162 CRC tissues using immunohistochemistry. The overall survival rate in patients of HJURP high expression was higher than those in HJURP low expression in CRC. Suppressing HJURP expression decreased cellular proliferation, invasion, and migration in four CRC cell lines: HT29, HCT116, SW480, SW620 in vitro study. Our findings revealed that the knockdown of HJURP suppressed the proliferation, migration, invasion, and tumorigenicity in CRC cells. Due to its strong association with CRC, HJURP could be a potential prognostic biomarker and a novel target for drug discovery.
All Author(s)
D. H. Kang ; J. Woo ; H. Kim ; S. Y. Kim ; S. Ji ; G. Jaygal ; T. S. Ahn ; H. J. Kim ; H. J. Kwak ; C. J. Kim ; M. J. Baek ; D. Jeong
Issued Date
2020
Type
Article
Keyword
Biomarkers, Tumor/*metabolismCell Line, TumorCell MovementCell ProliferationColorectal Neoplasms/metabolism/*surgeryDNA-Binding Proteins/*metabolismFemaleGene Expression Regulation, NeoplasticHCT116 CellsHT29 CellsHumansMalePrognosisSurvival AnalysisTreatment Outcome*Up-RegulationColorectal cancer (CRC)Hjurpprognostic biomarker
ISSN
1422-0067
Citation Title
International Journal of Molecular Sciences
Citation Volume
21
Citation Number
21
Citation Start Page
7928
Citation End Page
7928
Language(ISO)
eng
DOI
10.3390/ijms21217928
URI
http://schca-ir.schmc.ac.kr//handle/2022.oak/314
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