» Articles » PMID: 31007778

KIF23 Promotes Gastric Cancer by Stimulating Cell Proliferation

Overview
Journal Dis Markers
Publisher Wiley
Specialty Biochemistry
Date 2019 Apr 23
PMID 31007778
Citations 29
Authors
Affiliations
Soon will be listed here.
Abstract

Gastric cancer (GC) is one of the most aggressive malignant tumors with low early diagnosis and high metastasis. Despite progress in treatment, to combat this disease, a better understanding of the underlying mechanisms and novel therapeutic targets is needed. KIF23, which belongs to the KIF family, plays a vital role in various cell processes, such as cytoplasm separation and axon elongation. Nowadays, KIF23 has been found to be highly expressed in multiple tumor tissues and cells, suggesting a potential link between KIF23 and tumorigenesis. Herein, we reported that KIF23 expression was correlated with poor prognosis of gastric cancer and found an association between KIF23 and pTNM stage. An in vitro assay proved that the proliferation of gastric cancer cells was significantly inhibited, which is caused by KIF23 depletion. Additionally, knockdown of KIF23 resulted in a marked inhibition of cell proliferation of gastric cancer in mice, with significant downregulation of Ki67 and PCNA expression. In conclusion, these data indicate that KIF23 is a potential therapeutic target for gastric cancer treatment.

Citing Articles

KIFC3 promotes the progression of non-small cell lung cancer cells through the PI3K/Akt pathway.

Mu Y, Liu H, Luo A, Zhang Q Thorac Cancer. 2024; 15(33):2356-2364.

PMID: 39390964 PMC: 11586134. DOI: 10.1111/1759-7714.15465.


Diagnostic biomarker KIF23 is associated with immune infiltration and immunotherapy response in gastric cancer.

Bai M, Liu X Front Oncol. 2023; 13:1191009.

PMID: 37483517 PMC: 10361780. DOI: 10.3389/fonc.2023.1191009.


A Comprehensive Pan-Cancer Analysis Identifies CEP55 as a Potential Oncogene and Novel Therapeutic Target.

Zaki M, Eldeen M, K Abdulsahib W, Shati A, Alqahtani Y, Al-Qahtani S Diagnostics (Basel). 2023; 13(9).

PMID: 37175004 PMC: 10178510. DOI: 10.3390/diagnostics13091613.


Kinesin family member 23 knockdown inhibits cell proliferation and epithelial-mesenchymal transition in esophageal carcinoma by inactivating the Wnt/β-catenin pathway.

Xu Q, Li X, Li Y, Yu J, Yang A Funct Integr Genomics. 2023; 23(2):154.

PMID: 37162618 DOI: 10.1007/s10142-023-01088-y.


Integration of Chemoinformatics and Multi-Omics Analysis Defines ECT2 as a Potential Target for Cancer Drug Therapy.

Soltan M, Eldeen M, Sajer B, Abdelhameed R, Al-Salmi F, Fayad E Biology (Basel). 2023; 12(4).

PMID: 37106813 PMC: 10135641. DOI: 10.3390/biology12040613.


References
1.
Yang H, Chen Y, Takita J, Soeda E, Piao H, Hayashi Y . Genomic structure and mutational analysis of the human KIF1B gene which is homozygously deleted in neuroblastoma at chromosome 1p36.2. Oncogene. 2001; 20(36):5075-83. DOI: 10.1038/sj.onc.1204456. View

2.
Yu Y, Feng Y . The role of kinesin family proteins in tumorigenesis and progression: potential biomarkers and molecular targets for cancer therapy. Cancer. 2010; 116(22):5150-60. DOI: 10.1002/cncr.25461. View

3.
Valk K, Vooder T, Kolde R, Reintam M, Petzold C, Vilo J . Gene expression profiles of non-small cell lung cancer: survival prediction and new biomarkers. Oncology. 2011; 79(3-4):283-92. DOI: 10.1159/000322116. View

4.
Lee M, Choi D, Park M, Lee M . Gastric cancer: imaging and staging with MDCT based on the 7th AJCC guidelines. Abdom Imaging. 2011; 37(4):531-40. DOI: 10.1007/s00261-011-9780-3. View

5.
Duangtum N, Junking M, Sawasdee N, Cheunsuchon B, Limjindaporn T, Yenchitsomanus P . Human kidney anion exchanger 1 interacts with kinesin family member 3B (KIF3B). Biochem Biophys Res Commun. 2011; 413(1):69-74. DOI: 10.1016/j.bbrc.2011.08.050. View