» Articles » PMID: 34834441

Potential Prognostic Biomarkers of NIMA (Never in Mitosis, Gene A)-Related Kinase (NEK) Family Members in Breast Cancer

Overview
Journal J Pers Med
Date 2021 Nov 27
PMID 34834441
Citations 47
Authors
Affiliations
Soon will be listed here.
Abstract

Breast cancer remains the most common malignant cancer in women, with a staggering incidence of two million cases annually worldwide; therefore, it is crucial to explore novel biomarkers to assess the diagnosis and prognosis of breast cancer patients. NIMA-related kinase (NEK) protein kinase contains 11 family members named NEK1-NEK11, which were discovered from ; however, the role of NEK family genes for tumor development remains unclear and requires additional study. In the present study, we investigate the prognosis relationships of NEK family genes for breast cancer development, as well as the gene expression signature via the bioinformatics approach. The results of several integrative analyses revealed that most of the NEK family genes are overexpressed in breast cancer. Among these family genes, overexpression had poor prognostic significance in distant metastasis-free survival (DMFS) in breast cancer patients. Meanwhile, had the highest level of DNA methylation, and the functional enrichment analysis from MetaCore and Gene Set Enrichment Analysis (GSEA) suggested that was associated with the cell cycle, G2M checkpoint, DNA repair, E2F, MYC, MTORC1, and interferon-related signaling. Moreover, Tumor Immune Estimation Resource (TIMER) results showed that the transcriptional levels of NEK2 were positively correlated with immune infiltration of B cells and CD4 T Cell. Collectively, the current study indicated that family genes, especially which is involved in immune infiltration, and may serve as prognosis biomarkers for breast cancer progression.

Citing Articles

ST3GAL4 promotes tumorigenesis in breast cancer by enhancing aerobic glycolysis.

Chen X, Su W, Chen J, Ouyang P, Gong J Hum Cell. 2024; 38(1):1.

PMID: 39422756 DOI: 10.1007/s13577-024-01137-z.


Role of NEK2 in tumorigenesis and tumor progression.

Xia J, Zhao H, Edmondson J, Koss B, Zhan F Trends Mol Med. 2024; 31(1):79-93.

PMID: 39181803 PMC: 11717647. DOI: 10.1016/j.molmed.2024.07.013.


Glucosylceramide synthase modulation ameliorates murine renal pathologies and promotes macrophage effector function in vitro.

Cheong A, Craciun F, Husson H, Gans J, Escobedo J, Chang Y Commun Biol. 2024; 7(1):932.

PMID: 39095617 PMC: 11297156. DOI: 10.1038/s42003-024-06606-7.


Identification of metastasis-related genes for predicting prostate cancer diagnosis, metastasis and immunotherapy drug candidates using machine learning approaches.

Wang Y, Ji B, Zhang L, Wang J, He J, Ding B Biol Direct. 2024; 19(1):50.

PMID: 38918844 PMC: 11197330. DOI: 10.1186/s13062-024-00494-x.


Comprehensive bioinformatics analysis of human cytomegalovirus pathway genes in pan-cancer.

Yan T, Pang X, Liang B, Meng Q, Wei H, Li W Hum Genomics. 2024; 18(1):65.

PMID: 38886862 PMC: 11181644. DOI: 10.1186/s40246-024-00633-5.


References
1.
Wu L, Saxena S, Goel P, Prajapati D, Wang C, Singh R . Breast Cancer Cell-Neutrophil Interactions Enhance Neutrophil Survival and Pro-Tumorigenic Activities. Cancers (Basel). 2020; 12(10). PMC: 7599756. DOI: 10.3390/cancers12102884. View

2.
Disis M, Stanton S . Triple-negative breast cancer: immune modulation as the new treatment paradigm. Am Soc Clin Oncol Educ Book. 2015; :e25-30. DOI: 10.14694/EdBook_AM.2015.35.e25. View

3.
Cirillo E, Parnell L, Evelo C . A Review of Pathway-Based Analysis Tools That Visualize Genetic Variants. Front Genet. 2017; 8:174. PMC: 5681904. DOI: 10.3389/fgene.2017.00174. View

4.
Pavan I, Peres de Oliveira A, Dias P, Basei F, Issayama L, de Castro Ferezin C . On Broken Ne(c)ks and Broken DNA: The Role of Human NEKs in the DNA Damage Response. Cells. 2021; 10(3). PMC: 7997185. DOI: 10.3390/cells10030507. View

5.
Lee K, Kuo Y, Ho Y, Huang Y . Triple-Negative Breast Cancer: Current Understanding and Future Therapeutic Breakthrough Targeting Cancer Stemness. Cancers (Basel). 2019; 11(9). PMC: 6769912. DOI: 10.3390/cancers11091334. View