Identification of prognostic marker genes in head and neck squamous cell carcinoma: A study based on The Cancer Genome Atlas database and experimental validation

被引:2
作者
Zhong, Qilong [1 ]
Zhou, Li [2 ]
Zhu, Dan [1 ]
机构
[1] Maoming Peoples Hosp, Dept Ear Nose Throat, 101,Weimin Rd, Maoming 525000, Guangdong, Peoples R China
[2] Maoming Peoples Hosp, Dept Urol, Maoming, Peoples R China
关键词
head and neck squamous cell carcinoma; Kaplan‐ meier survival curve; pearson correlation coefficient; prognostic marker genes; prognostic risk assessment model; POOR-PROGNOSIS; DOWN-REGULATION; EXPRESSION; OVEREXPRESSION; GROWTH; PROLIFERATION; RESISTANCE; HOXC13-AS; EOTAXIN-1; BIOMARKER;
D O I
10.1111/jop.13186
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background Early detection and prognostic prediction are crucial in improving the survival of patients with head and neck squamous cell carcinoma (HNSCC). Therefore, we provided potential molecular markers in this study for early diagnosis and prognosis of this cancer based on The Cancer Genome Atlas (TCGA) database analysis and experimental validations. Methods Differentially expressed genes (DEGs) between HNSCC tumor and normal samples were identified by TCGA database-based analyses. Univariate and multivariate Cox regression analyses were applied, respectively, to identify survival-related DEGs and independent prognostic factors in HNSCC. Further, RT-qPCR was employed to verify expression of DEGs in cancer and adjacent tissues from HNSCC patients recruited in our hospital, in which we also clarified the correlation between candidate genes and clinicopathological characteristics and prognosis of HNSCC patients. Results TCGA data analyses yielded 59 DEGs. Cox analyses identified 13 candidate genes closely related to prognosis of HNSCC patients and established a five-gene signature comprising AC103702.2, LINC00941, RPL29, FOXL2, and CCL11. This five-gene signature could classify patients into high- and low-risk groups. The survival rate of the high-risk group was significantly lower than that of the low-risk group. Clinical tissue experiments further confirmed that AC103702.2, LINC00941, CCL11, and RPL29P19 genes were inversely associated with the prognosis of HNSCC patients, while CCL11 gene was positively associated. We also found that high-risk HNSCC patients presented a higher incidence of lymph node metastasis. Conclusion Five prognostic marker genes (AC103702.2, LINC00941, CCL11, RPL29P19, and FOXL2) as a gene cluster may serve as prognostic marker genes in HNSCC.
引用
收藏
页码:891 / 901
页数:11
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