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The clinical significance of apolipoprotein L1 in head and neck squamous cell carcinoma
Author(s) -
Feng Zhong,
Huiping Lu,
Gang Chen,
YiWu Dang,
Xiao-Guohui Zhang,
Yao Liang,
Mingxuan Li,
Guosheng Li,
Xiaoyi Chen,
Yuxuan Yao,
YongYing Qin,
Miao Mo,
Kai-Lang Zhang,
Hua Ding,
ZhiGuang Huang,
ZhuXin Wei
Publication year - 2020
Publication title -
oncology letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.766
H-Index - 54
eISSN - 1792-1082
pISSN - 1792-1074
DOI - 10.3892/ol.2020.12240
Subject(s) - head and neck squamous cell carcinoma , carcinogenesis , cancer , oncogene , cancer research , immunohistochemistry , molecular medicine , biology , cell cycle , tissue microarray , pathology , biomarker , downregulation and upregulation , head and neck cancer , oncology , medicine , gene , biochemistry
Approximately 500,000 new head and neck squamous cell carcinoma (HNSCC) cases are detected every year around the world, and its incidence ranks sixth among all cancer types globally. Among these cases, oral squamous cell carcinoma (OSCC) and laryngeal squamous cell carcinoma (LSCC) are HNSCC subtypes with high incidence rates, especially in China. The present study examines the association between the apolipoprotein L1 (APOL1) mRNA and protein expression and clinical parameters in HNSCC. The two most common types (oral and larynx) of HNSCC were selected for subgroup analyses. Immunohistochemistry (IHC) was used to detect APOL1 protein expression levels in HNSCC clinical specimens. It was demonstrated that APOL1 protein expression in 221 cases of HNSCC was higher compared with that in normal tissues. Consistent upregulation of APOL1 protein was also found in subgroups of OSCC and LSCC. Through mining the ArrayExpress, The Cancer Genome Atlas and the Gene Expression Omnibus databases, microarrays and RNA sequencing data for HNSCC were retrieved, which were used to analyze APOL1 mRNA expression levels. The results showed that APOL1 expression was higher in both OSCC and LSCC subtypes, as well as in HNSCC, compared with that in non-cancerous squamous epithelium. The summary receiver operating characteristic analysis showed that APOL1 had potential as a diagnostic biomarker for HNSCC, OSCC and LSCC. Thus, upregulation of APOL1 may contribute to the tumorigenesis of HNSCC.

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