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

  • Rainer Marco Lopez Lapa
  • , Mateus Camargo Barros-Filho
  • , Fabio Albuquerque Marchi
  • , Maria Aparecida Custódio Domingues
  • , Genival Barbosa de Carvalho
  • , Sandra Aparecida Drigo
  • , Luiz Paulo Kowalski
  • , Silvia Regina Rogatto*
  • *Kontaktforfatter
  • A.C.Camargo Cancer Center
  • São Paulo State University

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

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Abstract

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.

OriginalsprogEngelsk
TidsskriftOral Oncology
Vol/bind93
Sider (fra-til)76-84
ISSN1368-8375
DOI
StatusUdgivet - 1. jun. 2019

Finansiering

We are thankful for the A.C. Camargo Cancer Center Biobank for providing and processing the samples. We also thank Ana Hatagima ( in memorium ), Eliane P Ambrosio and Fabiola Encinas Rosa for their contribution during the study. This study was supported by grants from the National Institute of Science and Technology in Oncogenomics (INCITO - Fundação de Amparo à Pesquisa do Estado de São Paulo - FAPESP 2008/57887-9 and Conselho Nacional de Desenvolvimento Científico e Tecnológico - CNPq 573589/08-9 ). RML Lopez received fellowship from CNPq (# 153142/2012-0 ).

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