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Prognostic significance of KIF23 expression in gastric cancer

BACKGROUND: Kinesin super family 23 (KIF23) is a member of the KIF family, and it plays an important role in mitosis and cytokinesis. Loss of expression can cause mitotic arrest. The Oncomine database is one of the largest oncogene chip databases in the world, and is an integrated data mining platfo...

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Autores principales: Liang, Wei-Tian, Liu, Xiao-Fang, Huang, Hai-Bo, Gao, Zi-Ming, Li, Kai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7579732/
https://www.ncbi.nlm.nih.gov/pubmed/33133380
http://dx.doi.org/10.4251/wjgo.v12.i10.1104
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author Liang, Wei-Tian
Liu, Xiao-Fang
Huang, Hai-Bo
Gao, Zi-Ming
Li, Kai
author_facet Liang, Wei-Tian
Liu, Xiao-Fang
Huang, Hai-Bo
Gao, Zi-Ming
Li, Kai
author_sort Liang, Wei-Tian
collection PubMed
description BACKGROUND: Kinesin super family 23 (KIF23) is a member of the KIF family, and it plays an important role in mitosis and cytokinesis. Loss of expression can cause mitotic arrest. The Oncomine database is one of the largest oncogene chip databases in the world, and is an integrated data mining platform for cancer gene information. By querying the database, differences in expression between tumor tissue and normal tissue can be determined. AIM: To study the expression and prognostic significance of KIF23 in gastric cancer (GC). METHODS: We used immunohistochemistry to compare the expression of KIF23 in GC and normal gastric tissues. We mined the data on the expression and prognosis of KIF23 in GC using Oncomine and Kaplan–Meier plotter database. RESULTS: Compared with normal gastric tissues, KIF23 expression was increased in GC tissues, and correlated with T, N, and tumor–node–metastasis stages. Survival analysis showed that patients with high expression of KIF23 had a poor overall survival. There were five studies in the Oncomine database in which expression of KIF23 was significantly higher in GC tissues than in normal gastric tissues (P < 0.05). Kaplan–Meier plotter database analysis showed that recurrence-free survival, overall survival, distant metastasis free survival, and post progression survival of patients with high expression of KIF23 were lower than those of patients with low expression. Further stratified analysis found that prognostic survival indicators worsened in patients with T2 and T3 poorly differentiated adenocarcinoma with high expression of KIF23. CONCLUSION: KIF23 is highly expressed in GC and is associated with a poor prognosis of patients. It may be of great significance in the diagnosis, treatment, and prognostic evaluation of GC.
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spelling pubmed-75797322020-10-29 Prognostic significance of KIF23 expression in gastric cancer Liang, Wei-Tian Liu, Xiao-Fang Huang, Hai-Bo Gao, Zi-Ming Li, Kai World J Gastrointest Oncol Basic Study BACKGROUND: Kinesin super family 23 (KIF23) is a member of the KIF family, and it plays an important role in mitosis and cytokinesis. Loss of expression can cause mitotic arrest. The Oncomine database is one of the largest oncogene chip databases in the world, and is an integrated data mining platform for cancer gene information. By querying the database, differences in expression between tumor tissue and normal tissue can be determined. AIM: To study the expression and prognostic significance of KIF23 in gastric cancer (GC). METHODS: We used immunohistochemistry to compare the expression of KIF23 in GC and normal gastric tissues. We mined the data on the expression and prognosis of KIF23 in GC using Oncomine and Kaplan–Meier plotter database. RESULTS: Compared with normal gastric tissues, KIF23 expression was increased in GC tissues, and correlated with T, N, and tumor–node–metastasis stages. Survival analysis showed that patients with high expression of KIF23 had a poor overall survival. There were five studies in the Oncomine database in which expression of KIF23 was significantly higher in GC tissues than in normal gastric tissues (P < 0.05). Kaplan–Meier plotter database analysis showed that recurrence-free survival, overall survival, distant metastasis free survival, and post progression survival of patients with high expression of KIF23 were lower than those of patients with low expression. Further stratified analysis found that prognostic survival indicators worsened in patients with T2 and T3 poorly differentiated adenocarcinoma with high expression of KIF23. CONCLUSION: KIF23 is highly expressed in GC and is associated with a poor prognosis of patients. It may be of great significance in the diagnosis, treatment, and prognostic evaluation of GC. Baishideng Publishing Group Inc 2020-10-15 2020-10-15 /pmc/articles/PMC7579732/ /pubmed/33133380 http://dx.doi.org/10.4251/wjgo.v12.i10.1104 Text en ©The Author(s) 2020. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Basic Study
Liang, Wei-Tian
Liu, Xiao-Fang
Huang, Hai-Bo
Gao, Zi-Ming
Li, Kai
Prognostic significance of KIF23 expression in gastric cancer
title Prognostic significance of KIF23 expression in gastric cancer
title_full Prognostic significance of KIF23 expression in gastric cancer
title_fullStr Prognostic significance of KIF23 expression in gastric cancer
title_full_unstemmed Prognostic significance of KIF23 expression in gastric cancer
title_short Prognostic significance of KIF23 expression in gastric cancer
title_sort prognostic significance of kif23 expression in gastric cancer
topic Basic Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7579732/
https://www.ncbi.nlm.nih.gov/pubmed/33133380
http://dx.doi.org/10.4251/wjgo.v12.i10.1104
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