Published online Oct 15, 2020. doi: 10.4251/wjgo.v12.i10.1104
Peer-review started: April 14, 2020
First decision: May 15, 2020
Revised: May 29, 2020
Accepted: August 15, 2020
Article in press: August 15, 2020
Published online: October 15, 2020
Processing time: 183 Days and 3.2 Hours
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.
To study the expression and prognostic significance of KIF23 in gastric cancer (GC).
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.
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.
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.
Core Tip: This study investigated the role of the kinesin super family 23 (KIF23) in the gastric cancer (GC), including its expression and prognosis significance in GC. We found that 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. We believe that our study makes a significant contribution to the literature as it revealed a novel relationship between KIF23 and GC and may provide a new therapeutic target for treating GC.