Integrated miRNA and mRNA expression analysis uncovers drug targets in laryngeal squamous cell carcinoma patients

被引:23
|
作者
Lopez Lapa, Rainer Marco [1 ,2 ]
Barros-Filho, Mateus Camargo [1 ]
Marchi, Fabio Albuquerque [1 ]
Custodio Domingues, Maria Aparecida [3 ]
de Carvalho, Genival Barbosa [4 ]
Drigo, Sandra Aparecida [5 ]
Kowalski, Luiz Paulo [4 ]
Rogatto, Silvia Regina [5 ,6 ]
机构
[1] CIPE AC Camargo Canc Ctr, Int Res Ctr, Sao Paulo, Brazil
[2] Sao Paulo State Univ UNESP, Dept Genet, Inst Biosci, Botucatu, SP, Brazil
[3] Sao Paulo State Univ UNESP, Dept Pathol, Fac Med, Botucatu, SP, Brazil
[4] AC Camargo Canc Ctr, Dept Head & Neck Surg & Otorhinolaryngol, Sao Paulo, Brazil
[5] Sao Paulo State Univ UNESP, Dept Surg & Orthoped, Fac Med, Botucatu, SP, Brazil
[6] Univ Southern Denmark, Dept Clin Genet, Vejle Hosp, Inst Reg Hlth Res, Vejle, Denmark
基金
巴西圣保罗研究基金会;
关键词
Laryngeal squamous cell carcinoma; mRNA; miRNAs; Integrative analysis; Drug targets; Treatment; Chemotherapy; CANCER CELLS; ALPHA-V; ALK7; EXPRESSION; POOR-PROGNOSIS; HEAD; INVASION; OVEREXPRESSION; PROLIFERATION; METASTASIS; APOPTOSIS;
D O I
10.1016/j.oraloncology.2019.04.018
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: The current treatment of laryngeal squamous cell carcinoma (LSCC) is based on radical surgery and radiotherapy resulting in high morbidity. Chemoradiotherapy has been used as alternative to organ sparing; however, several advanced cases presented resistance to treatment, which contributes to a high risk of recurrence and mortality. Coding RNAs and miRNAs have potential to be used as biomarkers or targets for cancer therapy. Materials and Methods: In this study, 36 LSCC and 5 non-neoplastic control samples were investigated using miRNA and mRNA large-scale expression analysis and a cross-validation was performed using the TCGA database (116 LSCC and 12 surrounding normal tissues). Results: The large-scale profiling revealed the involvement of 28 miRNAs and 817 genes differentially expressed in LSCC. An integrative analysis comprising predicted and experimentally validated miRNA/mRNA interactions (negatively correlated), resulted in 28 miRNAs and 543 mRNAs. Decreased expression of miR-199b was significantly associated with shorter disease-free survival in LSCC (internal and TCGA datasets). The expression levels of selected miRNAs (miR-199b-5p, miR-29c-3p, miR-204-5p, miR-125b-5p and miR-92a-3p) and genes (COL3A1, COL10A1, ERBB4, HMGA2, HLF, TOP2A, MMP3, MMP13, MMP10 and PPP1R3) were confirmed as altered in LSCC by RT-qPCR. Additionally, a drug target prediction analysis revealed drug combinations based on miRNA and mRNA expression, pointing out novel alternatives to optimize the LSCC treatment. Conclusion: Collectively, these findings provide new insights in the LSCC transcriptional deregulation and potential drug targets.
引用
收藏
页码:76 / 84
页数:9
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