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

Oral Oncol

Department of Surgery and Orthopedics, Faculty of Medicine, São Paulo State University - UNESP, Botucatu, SP, Brazil; Department of Clinical Genetics, Vejle Hospital, Institute of Regional Health Research, University of Southern Denmark, Denmark. Electronic address:

Published: June 2019

AI Article Synopsis

  • The treatment for laryngeal squamous cell carcinoma (LSCC) is traditionally radical surgery and radiotherapy, but chemoradiotherapy shows promise despite resistance in advanced cases leading to recurrence and mortality.
  • A study analyzed 36 LSCC samples and found 28 involved miRNAs and 817 differentially expressed genes, with decreased miR-199b linked to shorter disease-free survival.
  • The research suggests potential biomarkers and drug targets to improve LSCC treatment, highlighting the need for new therapeutic strategies.

Article 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.

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Source
http://dx.doi.org/10.1016/j.oraloncology.2019.04.018DOI Listing

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