Characterization of KIF20B as a novel prognostic biomarker and therapeutic target for breast cancer
- PMID: 38426627
- DOI: 10.3892/ijo.2024.5631
Characterization of KIF20B as a novel prognostic biomarker and therapeutic target for breast cancer
Abstract
Despite advances in treatment and early detection, breast cancer remains one of the most common types of cancer and is the second leading cause of cancer death after lung cancer in women. Therefore, there is an urgent need to develop new biomarkers and therapeutic targets for the treatment of breast cancer. Based on gene expression profiles and subsequent screening performed in a preliminary study, kinesin family member 20B (KIF20B) was selected as a candidate target molecule, because it was highly and frequently expressed in all subtypes of breast cancer and barely detected in normal tissues. Reverse transcription‑quantitative PCR and western blotting revealed that KIF20B mRNA and protein expression levels were upregulated in most breast cancer cell lines but were scarcely expressed in normal mammary epithelial cells. Immunohistochemical staining of a tissue microarray showed that KIF20B was detected in 145 out of 251 (57.8%) breast cancer tissues. Strong KIF20B expression was significantly related to advanced pathological N stage. Moreover, patients with breast cancer and strong KIF20B expression exhibited a significantly worse prognosis than those with weak or negative KIF20B expression (P<0.0001, log‑rank test). In multivariate analysis, strong expression was an independent prognostic factor for patients with breast cancer. Furthermore, knockdown of KIF20B expression by small interfering RNA inhibited breast cancer cell proliferation and induced apoptosis. In addition, Matrigel cell invasion assays revealed that the invasiveness of breast cancer cells was significantly decreased by KIF20B silencing. Since KIF20B is an oncoprotein that is strongly expressed in highly malignant clinical breast cancer and serves a pivotal role in breast cancer cell proliferation, survival and invasion, KIF20B could be considered a candidate biomarker for prognostic prediction and a potential molecular target for developing new therapeutics, such as small molecule inhibitors, for a wide variety of breast cancers.
Keywords: KIF20B; biomarker; breast cancer; oncoantigen; therapeutic target.
Similar articles
-
Kinesin family member 20B regulates tongue cancer progression by promoting cell proliferation.Mol Med Rep. 2019 Mar;19(3):2202-2210. doi: 10.3892/mmr.2019.9851. Epub 2019 Jan 11. Mol Med Rep. 2019. PMID: 30664160 Free PMC article.
-
Characterization of KIF20A as a prognostic biomarker and therapeutic target for different subtypes of breast cancer.Int J Oncol. 2020 Jul;57(1):277-288. doi: 10.3892/ijo.2020.5060. Epub 2020 May 7. Int J Oncol. 2020. PMID: 32467984
-
KIF20B Correlates with LUAD Progression and Is an Independent Risk Factor.Crit Rev Eukaryot Gene Expr. 2024;34(3):49-59. doi: 10.1615/CritRevEukaryotGeneExpr.2023050271. Crit Rev Eukaryot Gene Expr. 2024. PMID: 38305288
-
Pseudopod-associated protein KIF20B promotes Gli1-induced epithelial-mesenchymal transition modulated by pseudopodial actin dynamic in human colorectal cancer.Mol Carcinog. 2018 Jul;57(7):911-925. doi: 10.1002/mc.22812. Epub 2018 Apr 10. Mol Carcinog. 2018. PMID: 29573464
-
KIF20B and MET, hub genes of DIAPHs, predict poor prognosis and promote pancreatic cancer progression.Pathol Res Pract. 2024 Feb;254:155046. doi: 10.1016/j.prp.2023.155046. Epub 2023 Dec 21. Pathol Res Pract. 2024. PMID: 38266456
Cited by
-
SEPT9: From pan-cancer to lung squamous cell carcinoma.BMC Cancer. 2024 Sep 5;24(1):1105. doi: 10.1186/s12885-024-12877-4. BMC Cancer. 2024. PMID: 39237897 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Molecular Biology Databases