Identification of SPRR3 as a novel diagnostic/prognostic biomarker for oral squamous cell carcinoma via RNA sequencing and bioinformatic analyses

被引:14
作者
Yu, Lu [1 ,2 ,3 ]
Yang, Zongcheng [1 ,2 ,3 ]
Liu, Yingjiao [4 ]
Liu, Fen [5 ]
Shang, Wenjing [5 ]
Shao, Wei [5 ]
Wang, Yue [5 ]
Xu, Man [6 ]
Wang, Ya-nan [1 ,2 ,3 ]
Fu, Yue [6 ]
Xu, Xin [1 ,2 ,3 ]
机构
[1] Shandong Univ, Dept Implantol, Sch & Hosp Stomatol, Jinan, Shandong, Peoples R China
[2] Shandong Univ, Shandong Prov Key Lab Oral Tissue Regenerat, Jinan, Shandong, Peoples R China
[3] Shandong Univ, Shandong Engn Lab Dent Mat & Oral Tissue Regenera, Jinan, Shandong, Peoples R China
[4] Univ Edinburgh, Coll Humanities & Social Sci, Sch Philosophy Psychol & Language Sci, Edinburgh, Midlothian, Scotland
[5] Shandong Univ, Sch Basic Med Sci, Dept Microbiol, Key Lab Expt Teratol,Chinese Minist Educ, Jinan, Shandong, Peoples R China
[6] Shandong Univ, Sch Med, Jinan, Shandong, Peoples R China
来源
PEERJ | 2020年 / 8卷
关键词
Oral squamous cell carcinoma; Bioinformatics; SPRR3; Biomarker; High-throughput RNA sequence; CORNIFIED ENVELOPE; STRING DATABASE; R PACKAGE; EXPRESSION; SURVIVAL; CANCER; GENES; ASSOCIATION; ENRICHMENT; SIGNATURE;
D O I
10.7717/peerj.9393
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Oral squamous cell carcinoma (OSCC) has always been one of the most aggressive and invasive cancers among oral and maxillofacial malignancies. As the morbidity and mortality of the disease have increased year by year, the search for a promising diagnostic and prognostic biomarker for the disease is becoming increasingly urgent. Tumorous and adjacent tissues were collected from three OSCC sufferers and we obtained 229 differentially expressed genes (DEGs) between tumor and normal tissues via high-throughput RNA sequence. Function and pathway enrichment analyses for DEGs were conducted to find a correlation between tumorigenesis status and DEGs. Protein interaction network and molecular complex detection (MCODE) were constructed to detect core modules. Two modules were enriched in MCODE. The diagnostic and prognostic values of the candidate genes were analyzed, which provided evidence for the candidate genes as new tumor markers. Small Proline Rich Protein 3 (SPRR3), a potential tumor marker that may be useful for the diagnosis of OSCC, was screened out. The survival analysis showed that SPRR3 under expression predicted the poor prognosis of OSCC patients. Further experiments have also shown that the expression of SPRR3 decreased as the malignancy of OSCC increased. Therefore, we believe that SPRR3 could be used as a novel diagnostic and prognostic tumor marker.
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页数:25
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